Ectrodactyly-ectodermal dysplasia-clefting syndrome (ECC) is a rare genetic disorder characterized by missing or malformed fingers and toes, abnormalities of skin, hair, nails, teeth, and cleft lip and/or palate. Affected individuals may have split hands, feet that turn inward, sparse hair, missing teeth, and defects in sweat and oil glands. The syndrome is caused by mutations in the TP63 gene and diagnosis is based on clinical signs and confirmed via genetic testing.
Ectrodactyly-ectodermal dysplasia-clefting syndrome (ECC) is a rare genetic disorder characterized by missing or malformed fingers and toes, abnormalities of skin, hair, nails, teeth, and cleft lip and/or palate. Affected individuals may have split hands, feet that turn inward, sparse hair, missing teeth, and defects in sweat and oil glands. The syndrome is caused by mutations in the TP63 gene and diagnosis is based on clinical signs and confirmed via genetic testing.
Ectrodactyly-ectodermal dysplasia-clefting syndrome (ECC) is a rare genetic disorder characterized by missing or malformed fingers and toes, abnormalities of skin, hair, nails, teeth, and cleft lip and/or palate. Affected individuals may have split hands, feet that turn inward, sparse hair, missing teeth, and defects in sweat and oil glands. The syndrome is caused by mutations in the TP63 gene and diagnosis is based on clinical signs and confirmed via genetic testing.