A Familial Case of Engelmann Disease with Hearing Impairment.
نویسندگان
چکیده
منابع مشابه
Angioid streaks in a case of Camurati–Engelmann disease
Camurati-Engelmann disease (CED) is a rare autosomal dominant disease with various phenotypic expressions. The hallmark of the disease is bilateral symmetric diaphyseal hyperostosis of the long bones with progressive involvement of the metaphysis. Ocular manifestations occur rarely and mainly result from bony overgrowth of the orbit and optic canal stenosis. We report a case of CED showing angi...
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ژورنال
عنوان ژورنال: Practica Oto-Rhino-Laryngologica
سال: 2002
ISSN: 1884-4545,0032-6313
DOI: 10.5631/jibirin.95.1005