The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition
pmid: 946410
The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition
Seven patients from four families are reported who had an inherited condition of which the main features were ankyloblepharon, ectodermal defects and cleft lip and palate. The ectodermal defects were partial or complete hair loss, absent or dystrophic nails, pointed widely spaced teeth and partial anhidrosis. Associated anomalies included lacrimal duct atresia, supernumerary nipples, syndactyly and auricular deformities. The inheritance of this abnormality was consistent with that of an autosomal dominant trait. The relationship between this and similar syndromes is discussed.
- Guy's and St Thomas' NHS Foundation Trust United Kingdom
- Guy's Hospital United Kingdom
- King's College Hospital NHS Foundation Trust United Kingdom
Adult, Chromosome Aberrations, Hypohidrosis, Male, Tooth Abnormalities, Cleft Lip, Eyelids, Infant, Nails, Malformed, Alopecia, Chromosome Disorders, Syndrome, Pedigree, Cleft Palate, Ectodermal Dysplasia, Child, Preschool, Humans, Female, Hair
Adult, Chromosome Aberrations, Hypohidrosis, Male, Tooth Abnormalities, Cleft Lip, Eyelids, Infant, Nails, Malformed, Alopecia, Chromosome Disorders, Syndrome, Pedigree, Cleft Palate, Ectodermal Dysplasia, Child, Preschool, Humans, Female, Hair
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