neuromuscular diagnosis in the modern era · neuromuscular diagnosis in the modern era kevin j....
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![Page 1: Neuromuscular Diagnosis in the Modern Era · Neuromuscular Diagnosis in the Modern Era Kevin J. Felice, D.O. Director, Charles H. Kaman Neuromuscular Center Hospital for Special Care](https://reader030.vdocuments.mx/reader030/viewer/2022040820/5e685eabcf85b218bc3ff020/html5/thumbnails/1.jpg)
Neuromuscular Diagnosis in the Modern Era
Kevin J. Felice, D.O.
Director, Charles H. Kaman Neuromuscular Center
Hospital for Special Care
Professor of Neurology
University of Connecticut School of Medicine Teaching Affiliate
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Neuromuscular Medicine
2005: Development
of automated and
Next Generation
DNA sequencing
Mid-1800: Duchenne &
Charcot introduce modern
clinicopathological methods
Mid-1900: Refinement of
muscle histopathology,
electron microscopy, and
electomyography
1987: Discovery of the
dystrophin gene by Kunkel,
Hoffman and Brown
1953: Discovery of DNA by
Watson and Crick
1990s: Progressive
Improvements in DNA
diagnosis
Time Line
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Hereditary Myopathies
• Duchenne muscular dystrophy (XR)
• Becker muscular dystrophy (XR)
• Facioscapulohumeral muscular dystrophy (AD)
• Emery-Dreifuss muscular dystrophy (XR)
• Myotonic dystrophy (Steinert disease) (AD)
• Limb-girdle muscular dystrophy (AD,AR,XR)
• Oculopharyngeal muscular dystrophy (AD)
• Congenital muscular dystrophy (AR)
• Congenital myopathies (AD,AR,XR)
• Myotonic congenita (AD,AR)
• Periodic paralyses (AD)
• Metabolic myopathies (AR)
• Mitochondrial myopathies (maternal)
• Distal myopathies (AD,AR)
Classification 1980
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Hereditary Myopathies
Muscular dystrophies
28 types
Congenital
muscular dystrophies
19 types
Congenital myopathies
20 types
Distal myopathies
10 types
Myotonic dystrophies
2 types
Metabolic myopathies
30 types
Mitochondrial myopathies
30 types
Channelopathies
4 types
Classification 2015
Genetic Neuromuscular Disorders
761 disease phenotypes
406 different genes
76 mapped loci awaiting gene identification
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Neuromuscular Disorders
• Neuromuscular history & exam
• Laboratory & genetic testing
• Neurophysiology/EMG
• Pathology of muscle, nerve, or skin
• Musculoskeletal & neuromuscular
imaging
Five Diagnostic Tools
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Neuromuscular Disorders
• Problems
– Phenotypic diversity
– Genetic diversity
– Cost of studies
• Solutions
– Careful exam
– Physician understanding of testing limitations
– Step-wise approach to testing
– Patient understanding & compliance
Five Diagnostic Tools
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Myopathy Evaluation
1. Proximal limb-girdle (e.g., BMD, LGMD)
2. Distal-predominant weakness (e.g., Miyoshi, Laing)
3. Proximal arm & distal leg (scapuloperoneal) (e.g., FSHD)
4. Distal arm & proximal leg (e.g., IBM, DM1)
5. Myopathies with blepharoptosis or ophthalmoparesis (e.g., OPMD,
DM1, CPEO)
6. Prominent neck extensor weakness (e.g., INEM, polymyositis)
7. Bulbar weakness (e.g., OPMD, LGMD1A)
8. Episodic weakness with rhabdomyolysis/myoglobinuria (e.g.,
McArdle disease, CPT2)
9. Episodic weakness unrelated to exercise (e.g., periodic paralyses)
10. Stiffness and decreased ability to relax (e.g., DM1, myotonia
congenita)
Patterns of Weakness
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Myopathy Evaluation
Pattern of weakness
Distal onset Proximal onset
Familial Acquired Familial Acquired
Muscular dystrophies
Congenital myopathies
Pompe disease
Polymyositis
Dermatomyositis
Toxic myopathies
Laing
Myoshi
Myofibrillar
Inclusion body
myositis
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Myopathy Evaluation
• Ptosis & ophthalmoplegia
– CPEO
– DM1
– OPMD
• Facial weakness
– FSHD
– OPMD
• Scapular winging
– FSHD
– LGMD2A
• Dysphagia
– OPMD
• Pseudohypertrophy
– Dystrophinopathy
• Contractures
– EDMD
– Ullrich
• Myotonia
– DM1
– DM2
• Fasciculations
– SMA
• Gynecomastia
– Kennedy
Phenotypic Features
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Phenotypic Diversity (Pleiotropy)
• Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD)
• Autosomal recessive EDMD (EDMD-AD) (H222Y)
• Autosomal dominant limb-girdle muscular dystrophy with cardiac conduction system disease (LGMD1B)
• Dilated cardiomyopathy with conduction system disease
• Dunnigan-type familial partial lipodystrophy
• Charcot-Marie Tooth neuropathy, axonal variant
• Mandibuloacral dysplasia, autosomal recessive
• Hutchinson-Gilford progeria
EDMD-AD
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Genetic Diversity
• Muscular dystrophies
– FSHD
– Scapuloperoneal MD
– Emery-Dreifuss MD
– LGMD (e.g., calpainopathy)
– Myotonic MD
• Metabolic myopathies
– PFK deficiency
– Acid maltase deficiency
• Congenital myopathies
– Nemaline rod
– Central core
– Myotubular
• Scapuloperoneal SMA
– Without sensory neuropathy
– With sensory neuropathy
(Davidenkow syndrome)
Disorders with Scapular Winging
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Neuromuscular Diagnosis
• Importance:
– Verify neuromuscular localization
– Focal neuropathies
– Polyneuropathy evaluation of demyelinating, axonal or
multifocal
– NMJ evaluation of pre- or post-synaptic
– Motor neuron diseases
– Myopathies associated with fibs, positive waves, or
myotonic discharges
• Limitations:
– Mild, metabolic or non-inflammatory myopathies
Neurophysiology
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Neuromuscular Diagnosis
• Types:
– Spinal imaging (MRI, CT) to assess for cord and root
disease
– Muscle imaging (MRI, US) to assess for pattern of
involvement
– Neurography (MRI, US) to assess for nerve entrapment,
edema or inflammation
• Limitations:
– Costs
– Availability of other tools
– Insurance coverage in US
Neuroimaging
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Muscle Biopsy
Surgical
specimen
Paraffin
sections
Frozen
sections
Immuno
sections
Electron
microscopy
Special
studies
Inflammation
Necrosis
Vasculitis
Histochemistry
Protein-based
analyses
Inclusions
Mitochondrial abn
Excess lipid or glycogen
Enzyme studies
DNA studies
Testing
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Muscle Biopsy
• Usually indicated
– Progressive myopathic weakness of unclear etiology
– History of exercise intolerance due to suspected metabolic or mitochondrial disorder
– Recurrent rhabdomyolysis
– Combined muscle & nerve biopsy in cases of suspected vasculitis
– HyperCKemia or myopathic EMG
– To search for suspected systemic disease with skeletal muscle manifestations – amyloid, sarcoid, mitochondrial cytopathy
• Usually not indicated
– When phenotype points to a specific genetic myopathy
– Motor neuron disease
– Polyneuropathy
– Myasthenic syndromes
– Myotonic disorders
– Channelopathies
Indications
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Muscle Biopsy
• Primary protein defects – Dystrophin: Xp21 muscular dystrophies
– Sarcoglycans: LGMD 2C-2F
– Dysferlin: LGMD2B, Miyoshi myopathy
– Caveolin-3: LGMD 1A, rippling muscle disease, idiopathic hyperCKemia
– Laminin 2: MDC1A (merosin-deficient MD)
– Collagen VI: Ullrich congenital muscular dystrophy
– Integrin 7: mild congenital MD
– Emerin: X-linked EDMD
– SERCA 1: Brody’s disease
– Plectin: Epidermolysis bullosa with muscular dystrophy
– Calpain-3: LGMD2A (immunoblot only)
• Secondary protein defects
– -dystroglycan: MDC1C (FRP), FCMD, MEB, WWS
– Laminin 2: MDC1B, LARGE, MDC1C, FCMD, MEB, WWS
– Sarcoglycans: LGMD 2C-2F
• Protein Accumulation
– Actin: congenital actinopathy, nemaline myopathy
– Myosin: Laing distal myopathy, myosin storage disease
– Desmin: myofibrillar myopathies
Immunohistochemistry
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nucleus
mitochondria
chromosome
gene
mitochondrial DNA
Organization of the Human Genome
>406 genes implicated in >761 NMD phenotypes
(Kaplan, www.musclegenetable.org)
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Human genome
Nuclear genome
~20,000 genes Mitochondrial genome
37 genes
• Only 1-2% of the entire genome is used for encoding proteins
• A large portion of the human genome is “repetitive DNA”
• Non-coding regions are involved in regulating gene function
Organization of the Human Genome
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Mutation
Chromosomal Molecular
Single-base substitutions Length variation
Genetic Defects
• Substitutions in the coding sequence
• Frameshift & premature termination of translation
• Repeat expansion
• Epigenetic silencing / activation
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Hereditary Myopathies
• Chromosomes
– Fluorescent in situ hybridization (FISH)
• DNA
– Restriction fragments (Southern blot analysis)
– PCR
– Sequencing
– Next-Gen panels
– Whole exome or genome sequencing
• mRNA
– Northern blot analysis
– Microarray expression analyses
• Protein
– Immunohistochemistry
– Enzyme assays
– Western blot analysis
Genetic Methods
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Neuromuscular Weakness
MND, PN, NMJ Disorder Myopathy
Clinical, EMG and lab assessment
Acquired Genetic
Specificity Highly Probable
Define clinical phenotype utilizing
EMG and muscle path if necessary
Specificity Possible Nonspecific Phenotype
Review clinical features and pedigree
Targeted DNA Testing Next-Gen Slice Whole exome sequencing
Diagnosis
+ -
Diagnosis
+
-
Diagnosis
+ -
Research
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Myopathy Evaluation
High specificity
1. Clinical Exam
--DMD
--FSHD1
--DM1
--OPMD
--EDMD
--Miyoshi
--McArdle
--Andersen
2. Clinical + Muscle Path
--DM2
--BMD
--GNE myopathy
--Pompe
3. Clinical + EMG
--DM2
--Myotonia congenita
Focused DNA testing
Diagnostic Approach
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Patient: AS (HSC36352)
• Referring service: general medicine
• Referring diagnosis: bilateral foot drop
• Patient: 45-yo woman
• Complaint:
– Progressive leg weakness, foot drop, and gait difficulties for 10
years
– Recent upper extremity weakness
– No pain or sensory symptoms
• Past medical history: right calf muscle biopsy 10 years ago (UVM)
• Family history:
– Born in India
– No weakness in unrelated parents, son, or relatives
History
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Patient: AS (HSC36352)
• Height & weight: 64 inches & 124 lb.
• CN: question mild lower facial weakness; weak whistle
• Motor
– Chair: slight hesitation
– Stance: mildly hyperlordosis
– Gait: steppage pattern
– Deep knee bend, tiptoes, heels: unable
– Strength: see MRC scores
– Atrophy: neck muscles; mild anterior foreleg atrophy; EDBs intact
– Positives: mildly winged & upwardly displaced scapulae
– Negatives: no pseudohypertrophy, scoliosis, contractures, fasciculations, or myotonia
• Sensory: normal
• Reflexes: hypoactive
• UMN or cerebellar signs: none
Exam
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Patient: AS (HSC36352)
MRC Score
UE R L LE R L
Arm abductors 4 4 Hip flexors 3 3
Arm flexors 5 5 Hip extensors 4 4
Arm extensors 5 5 Hip abductors 4 4
Wrist flexors 5 5 Hip adductors 3 3
Wrist extensors 5 5 Knee flexors 4 4
Finger flexors 5 5 Knee extensors 4 4
Finger extensors 4+ 4+ Foot dorsiflexors 2 2
Thumb extensors 5 5 Foot plantar flexors 4 4
Median FPL 5 5 Foot evertors 3 3
Median thenar 5 5 Foot invertors 4 4
Ulnar FDI 5 5 Toe flexors 4 4
Ulnar hypothenar 5 5 Toe extensors 3 3
Jamar grip forces (lb.) (RHD) 40 35 Toe abductors 2 2
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Myopathies & Vacuoles
• Storage diseases
– Glycogen storage (e.g., Pompe disease)
– Lipid storage (e.g., carnitine deficiency)
• Autophagic (rimmed) vacuoles
– Acquired myopathies (e.g., IBM)
– Hereditary myopathies (e.g., OPMD)
• Empty vacuoles
– Dilated t-tubules (e.g., periodic paralysis)
Types of Vacuoles
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Myopathies & Rimmed Vacuoles
• Hereditary inclusion body myopathies
– h-IBM2 or Nonaka myopathy
– h-IBM with Paget disease/FTD
– h-IBM3
• Distal myopathies
– Welander
– Markesbery-Griggs (ZASPopathy)
– Udd (titinopathy)
• Dystrophies
– LGMD1A (myotilin)
– LGMD2A (calpain)
– LGMD2G (telethoninopathy)
– EDMD
– FSHD
– OPMD
Disorders
• Sporadic inclusion body myositis (sIBM)
• Myofibrillar myopathy
– Myotilinopathy (LGMD1A)
– ZASPopathy
– Desminopathy
– Filaminopathy
– Bag3-opathy
– B-crystallin-opathy
– Reducing body myopathy (FHL1-opathy)
• Other myopathies
– Pompe disease
– Danon disease
– X-linked myopathy with excessive autophagy (VMA21)
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Distal-Onset Myopathies
• Hereditary distal myopathies
• Sporadic inclusion body
myositis
• Myotonic dystrophy type 1
• Facioscapulohumeral MD
• Oculopharyngeal MD
• Oculopharyngodistal MD
• Emery-Dreifuss MD
• Acid maltase deficiency
Disorders
• LGMD1A (myotilin)
• LGMD1C (caveolin-3)
• LGMD2A (calpain 3)
• LGMD2G (telethonin)
• Debrancher deficiency
• Nemaline myopathy
• Central core disease
• Myotubular myopathy
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Hereditary Distal Myopathies
Type Inheritance Locus (gene) Age Initial weakness
Welander AD 2p13 (TIA1) 40-60 Finger & wrist extensors
Udd (tibial muscular dystrophy)
AD 2q31 (titan) 35-50 Anterior foreleg
Markesbery AD 10q22.2 (ZASP) 40-50 Anterior foreleg
Laing AD 14q11.2 (MYH7) 3-25 Anterior foreleg, neck flexors
VCPDM AD 5q31 (matrin 3) 35-60 Anterior foreleg, finger extensors
Myofibrillar AD
AD
AD
AD
AD
AD
XR
AD
2q35 (desmin)
11q22 (-crystallin)
5q31 (myotilin)
10q22.2 (ZASP)
7q32 (filamin)
10q26.11 (BAG3)
Xq26.3 (FHL1)
7q36.3 (DNAJB6)
25-45 Hands or legs
Cardiomyopathy
HIBM2 (Nonaka, DMRV) AR 9p1-q1 (GNE) 15-30 Anterior foreleg
Miyoshi AR 2p13 (dysferlin) 15-30 Posterior foreleg
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Hereditary Distal Myopathies
Type CK Pathology
Welander 1-3X Dystrophic, rimmed vacuoles
Udd (tibial muscular dystrophy) 1-4X Dystrophic, rimmed vacuoles
Markesbery 1-4X Myofibrillar myopathy, dystrophic, rimmed vacuoles
Laing 1-3X Mild to moderate dystrophic, fiber type disproportion
VCPDM 1-3X Rimmed vacuoles
Myofibrillar 1-4X Myofibrillar myopathy, dystrophic, rimmed vacuoles
HIBM2 (Nonaka, DMRV) 3-4X Dystrophic, prominent rimmed vacuoles
Miyoshi 20-150X Dystrophic, dysferlin defect
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DNA Test
Patient: AS (HSC36352)
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HIBM
• Described by Argov (distal myopathy with rimmed vacuoles) in Israel and Nonaka in Japan in 1984
• Autosomal recessive
• Severe progressive myopathy with anterior foreleg-onset weakness, quadriceps-sparing
• Progresses to wheelchair in mean 12 years
• No bulbar, cardiac, or respiratory muscle involvement
• Caused by a deficiency in first enzyme in sialic acid biosynthetic pathway
• Defect leads to decreased sialylation of key proteins such as neural cell adhesion molecule (NCAM) and GM1
• Gene: (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase [GNE] at 9p1-q1
Features
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HIBM
• Affects diverse backgrounds – all ethnic groups
• Iranian Jews 1:1500 births
– Homozygous M712T mutation
• Japanese one frequent founder mutation V572L
• Multiple compound heterozygous missense mutations in kinase and epimerase domains of GNE in other ethnic groups
• Mutations in C-terminal domain (allosteric region) cause sialic storage disease
• About 400 cases reported in medical literature
• Survey of 400 clinics identified 146 patients
• Estimated 1600 to 2000 patients worldwide (1.4% of all myopathy patients)
Features
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Myopathy Evaluation
Moderate specificity
1. Clinical Exam
--LGMD
--EDMD
--Metabolic myopathy
--Hypertrophic cardiomyopathy
--Dilated cardiomyopathy
--Periodic paralyses
--Malignant hyperthermia
2. Clinical + Muscle Path
--Congenital myopathy
--Congenital muscular dystrophy
--Myofibrillar myopathy
--Lipid storage myopathy
--Distal myopathy
3. Clinical + EMG
--Unspecified myotonic disorder
DNA panel or slice
Diagnostic Approach
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Case 3: JR (UC090878)
• Referring service: general neurology
• Referring diagnosis: spinal muscular atrophy
• Patient: 37-yo man
• Complaint:
– Progressive leg weakness for 2 years
– Mild generalized weakness since childhood
– No pain or sensory symptoms
• Past medical history: unremarkable
• Family history: similar weakness in mother and multiple
maternal relatives
History
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Case 3: JR (UC090878)
Family History
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Case 3: JR (UC090878)
Family History
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?
?
I
II
III
IV
V
VI
1
1
2 3 4 5 6
8 9 10 11 12 13 2 3 4 5 6 7 14 15 16 17 18 19 20
1 2 3 4 5 6 7 8 9 10 11
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31
5 6 8 7 9 10 11 12
2 3 4 5 6 8 9 7 10
32 33 34 35
affected
reported to have “muscle weakness”
mental retardation – unknown etiology
13 14 15 1 2 3 4
1
examined √
√
√ √ √ √ √ √
√ √ √ √ √
√
sickle cell disease
? unknown if affected
2
5 ?
√
√
√
√
√ 18 22-26
12-13
17 21 20 19
11
16
Case 3: JR (UC090878)
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Case 3: JR (UC090878)
• Height & weight: 69 inches & 144 lb
• General: Normal
• CN: Normal
• Motor
– Difficulty arising from chair
– Lumbar hyperlordosis & protuberant abdomen
– Steppage pattern gait
– Atrophy of humeral, brachioradialis, hand, anterior foreleg, EDB
– Marked scapular winging
– No muscle pseudohypertrophy, gynecomastia, enlarged nerves, contractures, fasciculations, myotonia
• Sensory: Normal
• Reflexes: Diffusely hypoactive
• UMN signs: None
• Cerebellar signs: None
Exam
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Case 3: JR (UC090878)
• Upper extremity
– Arm abductors: 3/3
– Arm flexors: 3/3
– Arm extensors: 4/4
– Wrist flexors: 4/4
– Wrist extensors: 4/4
– Finger flexors: 2/2
– Finger extensors: 2/2
– Ulnar hand: 3/3
– Median hand: 3/3
– Grips (lb.): 25/25 (RHD)
• Lower extremity
– Hip flexors: 4/4
– Hip extensors: 4/4
– Hip abductors: 4/4
– Hip adductors: 4/4
– Knee flexors: 4/4
– Knee extensors: 4/4
– Plantar flexors: 4/4
– Foot extensors: 2/2
– Toe flexors: 3/3
– Toe extensors: 2/2
MRC Score (R/L)
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Genetic Diversity
• Muscular dystrophies
– FSHD
– Scapuloperoneal MD
– Emery-Dreifuss MD
– LGMD (e.g., calpainopathy)
– Myotonic MD
• Metabolic myopathies
– PFK deficiency
– Acid maltase deficiency
• Congenital myopathies
– Nemaline rod
– Central core
– Myotubular
• Scapuloperoneal SMA
Disorders with Scapular Winging
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Case 3: JR (UC090878)
• CK: 46 U/L (n<269)
• Other Labs: Normal
• FVC: 3.66 L (73%)
• NCS: Normal
• EMG:
– Mild myopathic changes
– No fibs, PSWs, myotonia, or fasciculations
• DNA tests (maternal aunt)
– FSHD: negative
– SMA: negative
Studies
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Myopathies
• Normal muscle fiber size:
– Males: 40-80 μm diameter
– Females: 30-70 μm diameter
– Mean size by type:
• Type 1: 52 μm
• Type 2: 59 μm
– Fiber type size difference: Mean diameters of type 1 and
type 2 fibers should not differ by more than 12% of the
largest diameter of the largest fiber type
Myofiber Size
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Muscle Fiber Type Atrophy
• Type I
– Myotonic dystrophy type I
– Congenital myopathies
• Central core disease
• Myotubular myopathy
• Centronuclear myopathy
• Nemaline myopathy
• Congenital fiber type
disproportion
• Congenital MYH7 myopathy
– Disuse (rare)
• Type II
– Disuse
– Aging
– Weight loss
– Systemic disease
– Stroke
– Myasthenia gravis
– Myotonic dystrophy type II
Considerations
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Congenital Myopathies
• Central core disease
• Nemaline myopathy
• Core-rod myopathy
• Centronuclear myopathy
• Multiminicore disease
• Congenital fiber-type
disproportion
• Reducing body myopathy
• Zebra body myopathy
• Fingerprint body myopathy
• Cytoplasmic body myopathy
• Tubular aggregate myopathy
• Type 1 fiber predominance
• Spheroid body myopathy
• Hyaline body myopathy
• Cap disease
• Sarcotubular myopathy
Classification
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Nemaline Myopathies
Type MIM# Inheritance
Chromosome
Gene Protein
NEM1 609284 AD 1q21.2 TPM3 -tropomyosin, slow
NEM2 256030 AR 2q22 NEB Nebulin
NEM3 161800 AD 1q42.1 ACTA1 actin 1 (skeletal muscle)
NEM4 609285 AD 9p13 TPM2 -tropomyosin
NEM5 605355 AR 19q13 TNNT1 troponin T type 1 (skeletal, slow)
NEM6 609273 AD 15q ? ?
NEM7 610687 AR 14q12 CFL2 cofilin 2 (muscle)
Classification
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ACTA1 Myopathies
• Nemaline myopathy
• Nemaline myopathy with cores
• Accumulation of thin filaments
• Congenital fiber-type disproportion
• Cap disease
Pathologic Changes
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CFTD
• ACTA1
• TPM3
• RYR1
• SEPN1
• MYH7
Implicated Genes
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Patient: RG (HSC44194)
• Referring service: neurology
• Referring diagnosis: myopathy
• Patient: 62-yo man
• Complaint:
– Mild leg weakness and gait imbalance for 5 years
– Difficulty climbing stairs
– Previously strong and physically active
• Past medical history:
– Hypertension, asthma,, elevated LFTs (2 negative liver biopsies), left
vastus lateralis muscle biopsy
• Family history:
– Mother had poliomyelitis
– Maternal uncle has multiple sclerosis
– 30-yo daughter is in good health
History
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Patient: RG (HSC44194)
• General:
– Large calf muscle
– No hand or foot deformities, scoliosis, winged scapulae, contractures,
gynecomastia
• Mental status: normal
• Cranial nerve: normal
• Motor:
– Mild waddling gait pattern
– Unable to perform deep knee bend
– Difficulty standing on tiptoes
– Mild proximal leg weakness
• Sensory: normal
• Reflexes: normal
Exam
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Patient: RG (HSC44194)
MRC Score
UE R L LE R L
Arm abductors 5 5 Hip flexors 4 4
Arm flexors 5 5 Hip extensors 5 5
Arm extensors 5 5 Hip abductors 5 5
Wrist flexors 5 5 Hip adductors 5 5
Wrist extensors 5 5 Knee flexors 5 5
Finger flexors 5 5 Knee extensors 5 5
Finger extensors 5 5 Foot dorsiflexors 5 5
Thumb extensors 5 5 Foot plantar flexors 5 5
Median FPL 5 5 Foot evertors 5 5
Median thenar 5 5 Foot invertors 5 5
Ulnar FDI 5 5 Toe flexors 5 5
Ulnar hypothenar 5 5 Toe extensors 5 5
Jamar grip forces (lb.) 102 86 Toe abductors 5 5
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Proximal Weakness
• Motor neuronopathies
– Spinal muscular atrophy
– Kennedy disease
– Amyotrophic lateral sclerosis
• Polyneuropathies
– CIDP/AIDP
– Diabetic amyotrophy
– Porphyria
• NMJ Disorders
– Myasthenia gravis
– Lambert-Eaton myasthenic syndrome
– Botulism
– Congenital myasthenic syndromes
Differential Diagnosis
• Myopathies
– Acquired
• Inflammatory myopathies
(PM/DM)
• Toxic myopathies (e.g., statins)
• Endocrine myopathies
– Genetic
• Muscular dystrophies
• Congenital myopathies
• Myotonic dystrophies
• Mitochondrial myopathies
• Myofibrillar myopathies
• Pompe disease
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Patient: RG (HSC44194)
• FVC: 3.34 L (76%)
• CK: 1450 U/L
• Echo/ECG: normal
• EMG: myopathic pattern with fibrillations and
positive sharp waves
• DNA:
– FSHD1: negative
– DM2: negative
Studies
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Myopathies
Cell-Based Classification
1. Disorders
2. Neurogenic
3. NMJ transmission
4. Sarcolemma
5. Nuclear proteins
6. Myofibrils
7. Intermediate filaments
8. Mitochondria
9. SR & t-tubules
10. Cytoplasmic proteins
11. Metabolic & storage disorders
12. DNA expansion disorders
13. FSHD
14. Inflammatory myopathies
15. Toxic myopathies
16. Aging and systemic disease
17. Rare structural abnormalities
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Neuromuscular Disorders
• Autosomal Dominant
– LGMD Type 1
– EDMD-AD
– FSHD1
– FSHD2
– Myotonic dystrophies type 1 & 2
– Congenital-AD
– OPMD
Muscular Dystrophies
• Autosomal Recessive
– LGMD Type 2
– EDMD-AR
– Congenital-AR
• X-Linked Recessive
– Duchenne
– Becker
– EDMD-XR
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Muscular Dystrophies
Name Inheritance Chromosome Gene Protein
LGMD1A AD 5q31 MYOT Myotilin
LGMD1B AD 1q22 LMNA Lamin A/C
LGMD1C AD 3p25 CAV3 Caveolin-3
LGMD1D AD 7q36.2 DNAJB6 DNAJB6
LGMD1E AD 2q35 DES Desmin
LGMD1F AD 7q32.1-q32.2 TNPO3 Transportin-3
LGMD1G AD 4q21 HNRPDL HNRPDL
LGMD1H AD 3p25.1-p23 ? ?
LGMD, Dominant
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Muscular Dystrophies
Name Inheritance Chromosome Gene Protein
LGMD2A AR 15q15.1 CAPN3 Calpain-3
LGMD2B AR 2p13 DYSF Dysferlin
LGMD2C AR 13q12 SGCG γ-SG
LGMD2D AR 17q12-q21.33 SGCA α-SG
LGMD2E AR 4q12 SGCB β-SG
LGMD2F AR 5q33 SGCD δ-SG
LGMD2G AR 17q12 TCAP Telethonin
LGMD2H AR 9q31.2 TRIM32 TRIM32
LGMD2I AR 19q13.3 FKRP Fukutin-related protein
LGMD2J AR 2q31 TTN Titin
LGMD, Recessive
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Muscular Dystrophies
Name Inheritance Chromosome Gene Protein
LGMD2K AR 9q34 POMT1 POMT1
LGMD2L AR 11p14.3 ANO5 Anoctamin 5
LGMD2M AR 9q31-q33 FKTN Fukutin
LGMD2N AR 14q24 POMT2 POMT2
LGMD2O AR 1p34 POMGNT1 POMGNT1
LGMD2Q AR 8q24 PLEC1 Plectin
LGMD2R AR 2q35 DES Desmin
LGMD2S AR 4q35.1 TRAPPC11 TRAPPC11
LGMD2T AR 3p21.31 GMPPB GMPPB
LGMD, Recessive
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Diagnosis: LGMD, type 2L (ANO5, 11p14.3)
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LGMD2L
• Rare autosomal recessive disorder
• Several large families reported of French-Canadian and Finnish ancestry
• Age of onset: 11-50 years
• Phenotype: proximal myopathy, proximal LE myopathy, quadriceps
myopathy, Miyoshi phenotype
• Progressive disorder – some patients wheelchair-bound after 12 years
• No clear genotype-phenotype correlation
• CK: normal to markedly elevated
• EMG: myopathic pattern with fibs and positive sharp waves
• Muscle biopsy: dystrophic pattern with fatty infiltration
• Anoctamin 5 protein is a complex glycoprotein localized in intracellular
vesicles, and has diverse cellular roles in the early development of the
musculoskeletal system
Features
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Myopathy Evaluation
Low specificity
1. Myopathy, unspecified
--Nonspecific clinical,
path and EMG findings
2. Neuromyopathy
--Possible myofibrillar or
mitochondrial disorder
3. Genetic or sporadic
non-inflammatory
myopathy, fixed or
metabolic, with negative
focused and/or panel
DNA studies
Exome or genome
sequencing
Diagnostic Approach
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Patient: HC (HSC50115)
• Referring service: neurology
• Referring diagnosis: myopathy
• Patient: 31-yo man
• Complaint:
– Progressive leg weakness for 10 years
– Difficulty performing job as letter carrier for 3 years
– Recent arm and hand weakness
– Occasional muscle aches and cramps
– No sensory symptoms
– No speech, swallowing or breathing difficulties
• Past medical history: negative
History
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Patient: HC (HSC50115)
Pedigree
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Patient: HC (HSC50115)
• General: thin body habitus, hypertelorism, pes
cavus, hammertoes
• Mental status: normal
• Cranial nerve: normal
• Sensory: mildly reduced toe vibration sensation
• Reflexes: absent
Exam
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Patient: HC (HSC50115)
• Motor exam
– Arise from chair: no difficulty
– Stance & base: normal
– Gait: mildly unsteady, steppage-pattern
– Deep knee bend: mild difficulty
– Standing on heels & tiptoes: unable
– Tandem-walking: mild difficulty
– Atrophy: trapezius, deltoid, medial pectoralis, humeral, distal quadriceps,
foreleg, foot muscles
– Mild scapular winging
• Studies
– FVC: 4.02 L (74%)
– CK: 1022 units/L (n<170)
Exam
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Patient: HC (HSC50115)
MRC Score
UE R L LE R L
Arm abductors 5 5 Hip flexors 5 5
Arm flexors 4 4 Hip extensors 5 5
Arm extensors 4 4 Hip abductors 5 5
Wrist flexors 5 5 Hip adductors 5 5
Wrist extensors 5 5 Knee flexors 5 5
Finger flexors 5 5 Knee extensors 4 4
Finger extensors 5 5 Foot dorsiflexors 2 2
Thumb extensors 5 5 Foot plantar flexors 3 3
Median FPL 5 5 Foot evertors 3 3
Median thenar 4 4 Foot invertors 3 3
Ulnar FDI 4 4 Toe flexors 2 2
Ulnar hypothenar 4 4 Toe extensors 2 2
Jamar grip forces (lb.) 54 44 Toe abductors 0 0
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NCSs
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CNE
Comment: Some areas in proximal limb muscles show increased (early) recruitment of small,
polyphasic MUAPs.
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CNE
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Patient: HC (HSC50115)
• CMT axonal DNA panel (15 genes): DNM2 VOUS
• Kennedy disease DNA: negative
• Pompe disease GAA blood spot: negative
• Myofibrillar myopathy DNA panel (6 genes): negative
• LGMD DNA panel (35 genes):
– COL6A2 G555R VOUS
– TTN E25692D VOUS
• mtDNA sequencing: MT-TR VOUS
• WES: POLG E1136K pathogenic variant (heterozygous)
• Diagnosis: mitochondrial neuromyopathy, POLG-related
Diagnostic Odyssey