An autosomal dominant disease characterized by autosomal dominant inheritance in tissues arising from the ectoderm including: ankyloblepharon filiforme adnatum and cleft lip and palate that has_material_basis_in heterozygous mutation in the TP63 gene on chromosome 3q27.
Synonyms
AEC syndrome,
ankyloblepharon-ectodermal defects-cleft lip and palate syndrome,
Hay-Wells syndrome
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