Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
<p>Abstract</p> <p>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 f...
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| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BMC
2011-05-01
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| Reeks: | Orphanet Journal of Rare Diseases |
| Onderwerpen: | |
| Online toegang: | http://www.ojrd.com/content/6/1/29 |
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