X-linked hypertrichosis

Chromosomal disorder From Wikipedia, the free encyclopedia

X-linked hypertrichosis

X-linked hypertrichosis, also known as X-linked congenital generalized hypertrichosis, is a hereditary disorders characterized by generalized congenital hypertrichosis and thick eyebrows.[1]

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X-linked hypertrichosis
Other namesX-linked congenital generalized hypertrichosis
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X-linked hypertrichosis is an X-linked dominant disorder.
SpecialtyDermatology
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Signs and symptoms

Hypertrichosis is characterized as excessive hair growth anywhere on the body, in either men or women.[2] X-linked hypertrichosis affects males more than females.[3]

Causes

X-linked hypertrichosis was first mapped in chromosome Xq24-q27.1 in a Mexican family; however, the underlying genetic facts remain unknown.[4] X-linked hypertrichosis is inherited in an X-linked dominant pattern of inheritance.[3]

See also

Further reading

  • DeStefano, Gina M.; Fantauzzo, Katherine A.; Petukhova, Lynn; Kurban, Mazen; Tadin-Strapps, Marija; Levy, Brynn; Warburton, Dorothy; Cirulli, Elizabeth T.; Han, Yujun; Sun, Xiaoyun; Shen, Yufeng; Shirazi, Maryam; Jobanputra, Vaidehi; Cepeda-Valdes, Rodrigo; Cesar Salas-Alanis, Julio; Christiano, Angela M. (2013-05-07). "Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis". Proceedings of the National Academy of Sciences. 110 (19): 7790–7795. doi:10.1073/pnas.1216412110. ISSN 0027-8424. PMC 3651487. PMID 23603273.
  • Figuera, Luis E.; Pandolfo, Massimo; Dunne, Patrick W.; Cantú, Jose M.; Patel, Pragna I. (1995). "Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24–q27.1". Nature Genetics. 10 (2). Springer Science and Business Media LLC: 202–207. doi:10.1038/ng0695-202. ISSN 1061-4036. PMID 7663516.

References

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