Labial Pits--Cleft Lip and/or Palate Syndrome: A Report of Five New Families

Abstract
Genealogical and clinical findings of five new families with the syndrome of pits of the lower lips and clefts of lip and palate (PiCLCP) suggest that the condition is transmitted as an autosomal dominant trait with—in most instances—complete penetrance of the mutant gene. The phenotype manifestations vary considerably from case to case. A satisfactory cosmetic result can be achieved by total excision of the pits provided one preserves the vermilion border.

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