-Gorlin syndrome- ندوة

Thursday 10 Nov 2022, 09:00 → 11:00 Asia/Baghdad

كلية طب الاسنان - قاعة فاضل القدسي - الطابق الارضي

م.م. رنا مرتضى

Gorlin syndrome, is a hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms.

Main clinical manifestations include multiple basal cell carcinomas (BCCs), odontogenic keratocysts of the jaws, hyperkeratosis of palms and soles, skeletal abnormalities, intracranial ectopic calcifications, and facial dysmorphism (macrocephaly, cleft lip/palate and severe eye anomalies).

Management requires a multidisciplinary approach and need Regular follow-up by a multi-specialist team (dermatologist, neurologist and odontologist).

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