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Results 1 - 10 of 19 for Alopecia
  1. ... are associated with an increased risk of androgenetic alopecia, a form of hair loss also known as male pattern baldness in men and female pattern hair loss in women. The variants change the number or ...
  2. ... VDR gene mutations impair hair growth, leading to hair loss (alopecia); however, mutations that block VDR's ability to interact with calcitriol do not cause alopecia, indicating that calcitriol is not necessary for the ...
  3. ... been found to cause T-cell immunodeficiency, congenital alopecia, and nail dystrophy, a condition that affects the ... a result, people with T-cell immunodeficiency, congenital alopecia, and nail dystrophy develop recurrent serious infections starting ...
  4. ... been found to cause palmoplantar keratoderma and congenital alopecia 1, a condition characterized by skin problems, an absence of hair from birth (congenital alopecia), and often nail abnormalities. The mutation identified in ...
  5. ... include features such as genital abnormalities in males, hair loss (alopecia), and enlarged parietal foramina (described above). The ALX4 ... the function of hair follicles and lead to alopecia, but the mechanism is unclear.Because enlarged parietal ...
  6. ... of stroke, deterioration of cognitive function (dementia), premature hair loss (alopecia), and attacks of low back pain. These signs ... of TGF-β signaling may also underlie the hair loss and back pain seen in people with CARASIL, ...
  7. ... have difficulty feeding, breathing problems, a skin rash, hair loss (alopecia), and a lack of energy (lethargy). If left ...
  8. ... DRB1*04:01). MedlinePlus Genetics provides information about Alopecia areata More About This Health Condition Certain variations ...
  9. ... of the barrier. MedlinePlus Genetics provides information about Alopecia areata More About This Health Condition Mutations in ...
  10. ... condition is characterized by delayed or absent puberty, hair loss, abnormal movements, hearing loss, and intellectual disability.Most ... in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome. Am ...
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