genetic disease comprendium

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Genetic Disease Comprendium Biology Period 2-3A 2011

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Genetic Disease Comprendium. Biology Period 2-3A 2011. Turner syndrome. The two main features of Turner syndrome is that they are shorter than average and small or bad development of ovaries. . - PowerPoint PPT Presentation

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Page 1: Genetic Disease  Comprendium

Genetic Disease Comprendium

Biology Period 2-3A2011

Page 2: Genetic Disease  Comprendium

Turner syndromeTurner syndrome is a chromosomal

condition that messes up development in females. Women with this condition tend to

be shorter than average.The two main features of Turner syndrome is that they are shorter than average and small or bad development of ovaries.

Turner syndrome is not usually inherited by the family. Turner syndrome occurs when one of the two X chromosomes normally found in women is missing or incomplete. Although the exact cause of Turner syndrome is not known.

Page 3: Genetic Disease  Comprendium

This is a genetic disease that causes thick, sticky mucus to build up in the

lungs, Digestive tracts and more parts of the human body. This

genetic disease is life-threatening.

Cystic fibrosisCystic fibrosis is passes down in families.

People who would be most likely to get this disease is young kids and young adults.

The disease can be treated though. A few ways this disease can be treated is by a prescribed antibiotics, inhaled medicines, or even a flu or pneumococcal vaccine.

<----- Cystic fibrosis can do this to your hands.

Above is a diagram of cystic fibrosis

By: Bridget Emmons, and Catherine Oakley

Above shows a diagram of mucus build up in the lungs and blockage of mucus in the pancreas

Page 4: Genetic Disease  Comprendium

NeurofibromatosisIt causes tumors that may be benign or may cause serious damage

• How is this disease inherited? – it is a autosomal dominate disorder: which means only one copy of the affected gene is needed for this disorder to develop.

• Are there certain people that are more prone to inheriting the disease? - if there patient has it they have a 50/50 chance of inheriting it.

• How is this disease treated?- there is no cure, only there is therapy to manage the symptoms and complications. Surgery may be needed.

• Cassie Scott and Samantha Arzie

Page 5: Genetic Disease  Comprendium

Canavan Disease by: Allie Brennan, Karley

Hilton.• It causes early childhood death.• This disease is inherited when babies inherit two nonworking copies

of the Canavan gene, they are not able to make enough ASPA. Without this enzyme, the body is not able to break down another substance, called NAA, which builds up and causes brain damage, mental retardation, tremors and an inability to move muscles.

• The certain people prone to inheriting this disease are estimated 1 in 40 Ashkenazi Jews is a carrier of the disease .Screening will detect about 97% of carriers.

• There is no current treatment for this disease.

Page 6: Genetic Disease  Comprendium

Alzheimer'sAlzheimer’s

Causes:-Memory Loss

-Thinking-Behavior

By: Isabel Engelbrekt & Kaeleigh Paternoster

Who Alzheimer’s affects:

-people of old age-people can also

have early onset of Alzheimer's at ages

40-50Treatment:-Currently there is

no cure-drug and non-

drug treatments may help with both cognitive and behavioral

symptoms

How Alzheimer’s is Inherited:

-an affected person inherits the altered

gene (which is sufficient to cause the disease)

from one parent-The inheritance pattern of late-onset Alzheimer disease is uncertain.

-People who inherit one copy of the APOE e4

allele have an increased chance of developing

the disease; those who inherit two copies of the

allele are at even greater risk.

This picture shows what areas of the brain are affected

Page 7: Genetic Disease  Comprendium

Tree Man Disease• Tree man disease is caused by

HPV a fairly common infection that usually causes sufferers to develop small warts.

• Although many affected persons inherit the disorder, between 30 and 50 percent of new cases arise spontaneously through mutation in an individuals genes.

• People who have HPV are more prone to getting this disease.

• Surgery is recommended to remove tumors from the nervous system.

• Caleb and Hunter

Page 8: Genetic Disease  Comprendium

AutismWhat is it?• Autism is a range of complex neurodevelopment disorders, characterized by social

impairments, communication difficulties, and restricted, repetitive, and stereotyped patterns of behavior.

How do you know:• no babbling or pointing by age 1 • no single words by 16 months or two-word phrases by age 2 • no response to name • loss of language or social skills • poor eye contact • excessive lining up of toys or objects • no smiling or social responsivenessCause:• Scientists aren’t certain about what causes autism.Cure:• There is no cure.

Page 9: Genetic Disease  Comprendium

Down SyndromeWhat does it cause:• Impulsive behavior• Poor judgment • Short attention spam• Slow learning How the disease is inherited:• There are 47 chromosomes instead of 46.• On the 21st chromosome there is an extra

copy, so there is 3 instead of 2.Treatment: • There is no specific treatment.• If one is born with gastrointestinal

blockage may need surgery. This disease does not affect certain people, it is just random.

Darby LeafMary YoungSam Briant

Page 10: Genetic Disease  Comprendium

By: Sam WilsonKatie Peacock

Riggs Long

Anemia

Page 11: Genetic Disease  Comprendium

• Anemia is caused by a decrease in production of red blood cell or hemoglobin.• Also it could be by a loss or

destruction of blood.

The causes of Anemia.

Page 12: Genetic Disease  Comprendium

• It’s inherited from your parents, in your genes.

How the disease is inherited.

Page 13: Genetic Disease  Comprendium

• Iron supplements

TREATMENTS

Page 14: Genetic Disease  Comprendium
Page 15: Genetic Disease  Comprendium

By: Travis BoothDan Whitney

Joey Clark

Achondroplasia(Dwarfism)

Page 16: Genetic Disease  Comprendium

• Achondroplasia is a genetic condition that results in abnormally short stature and is the most common cause of short stature with short limbs.

• The average height of an adult with Achondroplasia is 131 cm (52 inches, or 4 foot 4 inches) in males and 124 cm (49 inches, or 4 foot 1 inch) in females.

• Achondroplasia literally means without cartilage formation• Achondroplasia is one of the oldest known birth defects.

About Achondroplasia

Page 17: Genetic Disease  Comprendium

• Achondroplasia may be inherited as an autosomal dominant trait, that means that if a child gets the defective gene from one parent, the child will have the disorder. If one parent has Achondroplasia, the infant has a 50% chance of inheriting the disorder.

• If both parents have the condition, the infant's chances of being affected increase to 75%.

• In some conditions when neither of the parents have the disorder, there chances that the child is born with the disorder.

How is Achondroplasia Inherited?

Page 18: Genetic Disease  Comprendium

• For Achondroplasia anybody who is born with it more than likely will have offspring with the disorder as long as the other parent has the same disorder.

Are There Certain People Who Are Prone To Getting The Disease?

Page 19: Genetic Disease  Comprendium

• For this particular disease there is no actual treatment for it if you are born with it you stay with it.

How Is it treated

Page 20: Genetic Disease  Comprendium