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Ghita Filali Baba

Publications (1)

Expanding the Spectrum of Hay–wells Syndrome: A Trichoscopic Perspective

Rasha Moumna, Ouissal Essadeq, Ghita Filali Baba, Laila Benzekri & Nadia Ismaili · Asian Journal of Pediatric Research · 2025

Aims: Hay–Wells syndrome (ankyloblepharon–ectodermal dysplasia–clefting or AEC syndrome) is a rare autosomal dominant disorder caused by TP63 mutations, classically associated with skin, hair, nail, and craniofacial anomalies. Although hair abnormalities are commonly reported, th...

Open access Research Article 10.9734/ajpr/2025/v15i6455