Which genetic condition should I choose for a biology project? - m s condition_symptoms
Agammagoblulinemia
Albinism
ACU
Alzheimer's
Charcot-Marie-Tooth
Cleft lip and cleft palate
Clubfoot
Coffin-Lowry Syndrone
Blindness
Diabetes mellitus
Down Syndrome
Fragile X syndrome
Galactosemia
Glaucoma
Hereditary Deafness
Congenital cataracts
Hurler
Hypercholesterolemia
Hypertension
Maple syrup urine
Marfan Syndrome
Muscular dystrophy
Phenylketonuria
Progeria
Pyloric stenosis
Spina bifida
Thalassemia
Trisomy 9
Trisomy 13
Trisomy 18
Turner Syndrome
Tuberous sclerosis
Xeroderma pigmentosum
These are genetic diseases that I could choose, but you do not choose to May from a genetic disease in the list, as long as it does not use enough information for me to answer some questions.
These questions concern the effects of the disease, symptoms, treatment, mode of transmission and a large amount of genetic information to others to pass on the genetic origin, diagnosis, cure, or research for healing, is an expected lifespan / W person status, frequency, and a square canister to the possible outcomes for children, etc.
If anyone wants to know what specific questions, please contact a comment to know that I am after and I will try immediately to put matters
The genetic conditions that I can find important information? Please give me a number of conditions that are now my first choice, and please explain why it is not recommended. Thanks
Wednesday, January 6, 2010
M S Condition_symptoms Which Genetic Condition Should I Choose For A Biology Project?
3 comments:
I'd go with fragile X, it's a condition that not only has reprecussions on those with the condition but those who are carriers and the research is really taking off.
Time Article – Fragile X: Unraveling Autism's Secrets
http://www.time.com/time/magazine/article/0,9171,1818268,00.html
Time Article – A new approach to correcting autism
http://www.time.com/time/health/article/0,8599,1696451,00.html
http://www.seasidetherapeutics.com/
www.fraxa.org
www.fragilex.org
Hard to say, but if I did I really choose the Tay-Sachs disease, abbreviated (TSD, also known as GM2) gangliosidosis known hexosaminidase or loss.
It is an autosomal recessive genetic disease. Presented in its most common variant known Tay-Sachs child is a relentless deterioration of mental and physical abilities, from the age of 6 months and usually results in death at the age of four years.
The research in the late 20 Century demonstrated that Tay-Sachs is caused by a genetic mutation of the Hexa gene on chromosome 15th Been a large number of HEXA mutations discovered, and new ones are still reported. These mutations reach significant frequencies in various populations. The French Canadians of Quebec, the frequency of the carrier similar to the southeast Ashkenazi Jews, but they also carry another mutation. Many Cajuns in Louisiana, take in the south of the same mutation is more common in Ashkenazi Jews. Most HEXA mutations are rare and not in isolated populations of genetically manufactured. The disease can occur, possiblyInheritance of two independent mutations in the gene HEXA. This is one reason why it is so interesting, because they usually have the same mutation.
Until the 1970s and 80s, when they learned of the molecular genetics of disease, juvenile and adult disease is not always recognized as a variant of the TSD. Post-infantile Tay-Sachs disease is often diagnosed as other neurological disorders such as Friedreich's ataxia. [5] The patients are often filled with many people in wheelchairs, from time to adulthood, but many adults live lives that are located where the mental and physical difficulties. Psychiatric symptoms and seizures can be controlled by medication.
If you want to and need help, please let me know.
If you what to do, I want to say color-blindness, because I think it's fairly easy to understand, how it is transmitted, but with a little more difficult than you can know more than you would down with the syndrome.
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