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what kind of mutation is hypertrichosis

A 33-year-old female asked:
Dr. Michael Dugan
Specializes in Hematology
Yes: When the medication is stopped the hair will get better, and it may take a while.
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A 43-year-old member asked:
Dr. J. Lawrence Dohan
56 years experience Dermatology
Yes: Some people are very hairy. There are various causes and various manifestations.
A 33-year-old female asked:
Dr. Milroy Samuel
23 years experience Obstetrics and Gynecology
Perhaps : Usually time is the key. However everyone is different.
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A 50-year-old member asked:
Dr. Jefferson Chen
33 years experience Neurosurgery
Chromosome 17: Canavan's disease is an autosomal recessive inherited disease mapped to chromosome 17. This disorder falls into the family of leukodystrophies. This ... Read More
A 38-year-old member asked:
Dr. James Ferguson
45 years experience Pediatrics
Autosomal Dominant: The commonly seen form of achondroplasia is an autosomal dominant form of short limb dwarfism. 80% are new mutations but it can be passed parent to ch ... Read More
A 53-year-old member asked:
Dr. Christopher Abel
25 years experience Pediatrics
Depends: There are too many different types of scid - severe combined immunodeficiency for there to be just one mutation. Scid is commonly referred to as "bub ... Read More
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A 23-year-old female asked:
Dr. Elizabeth Wallen
34 years experience Pediatrics
Don't understand: What do you want explained?
A member asked:
Dr. Donald Nino
37 years experience Family Medicine
Hemophilia: A mutation on the x chromosome that affects the blood clotting factors viii or ix.
A 45-year-old member asked:
Dr. Lois Freisleben-Cook
40 years experience Pediatrics
Hemoglobin: formation is affected in thalassemia. Mutation in one or both of the genes responsible for the production of hemoglobin proteins (alpha and beta glo ... Read More
A 56-year-old member asked:
Dr. Johanna Fricke
49 years experience Developmental and Behavioral Pediatrics
X-linked mutation: Barth syndrome, also known as 3-methylglutaconic aciduria type II (MGCA2), is caused by mutation in the tafazzin gene (TAZ) on chromosome Xq28. Each b ... Read More

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