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Results 1 - 10 of 28 for hypothyroidism OR alopecia
  1. TSHB gene 
    ... least 10 TSHB gene mutations involved in congenital hypothyroidism, a condition characterized by abnormally low levels of ... a form of the condition called central congenital hypothyroidism, which occurs when stimulation of thyroid hormone production ...
    https://medlineplus.gov/genetics/gene/tshb - Genetics
  2. TSHR gene 
    ... mutations have been identified in people with congenital hypothyroidism, a condition characterized by abnormally low levels of ... levels remain low, causing mild to severe congenital hypothyroidism. Impaired thyroid stimulating hormone receptors may also disrupt ...
    https://medlineplus.gov/genetics/gene/tshr - Genetics
  3. TG gene 
    ... Mutations in the TG gene can cause congenital hypothyroidism, a condition characterized by abnormally low levels of ... not have other signs and symptoms of congenital hypothyroidism (described above). It is unclear why enlargement of ...
    https://medlineplus.gov/genetics/gene/tg - Genetics
  4. DUOX2 gene 
    ... identified several DUOX2 gene mutations that cause congenital hypothyroidism, a condition characterized by a reduction of thyroid ... hormone levels are extremely low, causing severe congenital hypothyroidism. If only one copy of the DUOX2 gene ...
    https://medlineplus.gov/genetics/gene/duox2 - Genetics
  5. TPO gene 
    ... cell membrane. TPO gene mutations can cause congenital hypothyroidism, a condition characterized by abnormally low levels of ... or reduced, leading to the features of congenital hypothyroidism. In most affected individuals, the thyroid gland is ...
    https://medlineplus.gov/genetics/gene/tpo - Genetics
  6. PAX8 gene 
    ... least 15 mutations in this gene cause congenital hypothyroidism, a condition characterized by abnormally low levels of ... Di Lauro R. PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis. Nat Genet. 1998 May; ...
    https://medlineplus.gov/genetics/gene/pax8 - Genetics
  7. FOXN1 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/foxn1 - Genetics
  8. SLC5A5 gene 
    ... mutations have been identified in people with congenital hypothyroidism, a condition characterized by abnormally low levels of ... thyroid hormones. The signs and symptoms of congenital hypothyroidism associated with these gene mutations range from mild ...
    https://medlineplus.gov/genetics/gene/slc5a5 - Genetics
  9. 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 ...
    https://medlineplus.gov/genetics/gene/vdr - Genetics
  10. GJA1 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics
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