Marie Unna congenital hypotrichosis
Congenital hypotrichosis characterized by little or no eyebrows, eyelashes, or body hair at birth, followed by the development of coarse, wiry, twisted hair in early childhood which progresses to ALOPECIA. Two genetically distinct forms exist; type I is caused by mutations in the hair growth associated (HR) gene. OMIM: 146550
Also Known As:
Hypotrichosis, Marie Unna type; Marie Unna hereditary hypotrichosis
Networked: 2
relevant articles (0 outcomes,
0 trials/studies)
Disease Context: Research Results
Experts
1. | Choi, Jee-Hyun:
1 article
(01/2018)
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2. | Choi, Keonwoo:
1 article
(01/2018)
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3. | Kim Yoon, Sungjoo:
1 article
(01/2018)
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4. | Kim, Eunmin:
1 article
(01/2018)
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5. | Kim, Injung:
1 article
(01/2018)
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6. | Kim, Jeong-Ki:
1 article
(01/2018)
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7. | Lee, Hwa-Young:
1 article
(01/2018)
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8. | Park, Jongkeun:
1 article
(01/2018)
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9. | Baek, In Cheol:
1 article
(06/2009)
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10. | Cha, Dal-Sun:
1 article
(06/2009)
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Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Marie Unna congenital hypotrichosis: