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Ichthyosis follicularis with alopecia and photophobia syndrome : ウィキペディア英語版 | Ichthyosis follicularis with alopecia and photophobia syndrome
IFAP syndrome is an extremely rare genetic syndrome. It is also known as Ichthyosis follicularis, alopecia, and photophobia syndrome or simply ichthyosis follicularis.〔James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.〕 It is extremely rare: there were only 10 known cases (all male) in 1998.〔OMIM (Online Mendelian Inheritance in Man), Johns Hopkins University, (Ichthyosis follicularis, atrichia and photophobia )〕 ==Symptoms== The main symptoms are given by its name: dry, scaly skin (ichthyosis), absence of hair (atrichia) and excessive sensitivity to light (photophobia). Additional features include short stature, mental retardation, seizures and a tendency for respiratory infections.〔
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