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Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
The IFAP syndrome is a rare X-linked genetic disorder reported in nearly 40 patients. It is characterized by the triad of Ichthyosis Follicularis, Alopecia, and Photophobia from birth. Other features such as short stature, intellectual disability, and seizures may develop in the first few years of l...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3127745/ https://ncbi.nlm.nih.gov/pubmed/21600032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-29 |
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