## A diagnosis of IFAP (ichthyosis follicularis with atrichia and photophobia) syndrome was established in a 1-year-old boy with congenital hairlessness, generalized ichthyotic skin changes with follicular hyperkeratoses, and photophobia. IFAP syndrome is considered to be an X-linked recessive tra
β¦ LIBER β¦
Ichthyosis follicularis with atrichia and photophobia (IFAP) syndrome in two unrelated female patients
β Scribed by Stefano Cambiaghi; Mauro Barbareschi; Gianluca Tadini
- Book ID
- 117845233
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- English
- Weight
- 124 KB
- Volume
- 46
- Category
- Article
- ISSN
- 1097-6787
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The syndrome of ichthyosis follicularis, alopecia, and photophobia (IFAP) is an uncommon neuroichthyosis described in only 10 males so far. We report on a man with congenital ichthyosis and alopecia with apparently normal development in early infancy. Photophobia and generalized myoclonicastatic sei