Rosselli-Gulienetti syndrome

A rare congenital ectodermal dysplasia syndrome with a range of signs and symptoms including cleft lip or palate, mental retardation and various forms of ectodermal dysplasia. Additional symptoms may include fused eyelids, absent nails, delayed bone growth and dry skin. It is believed that this syndrome follows an autosomal dominant pattern of inheritance with incomplete penetrance, and caused by a mutation affecting the TP63 gene

Also known as: Rosselli-Gulienetti syndrome

1 clinical trial for this condition and its sub-types, 0 tagged with Rosselli-Gulienetti syndrome itself.