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The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition.
Br J Dermatol. 1976 Mar; 94(3):277-89.BJ

Abstract

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.

Authors

No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

946410

Citation

Hay, R J., and R S. Wells. "The Syndrome of Ankyloblepharon, Ectodermal Defects and Cleft Lip and Palate: an Autosomal Dominant Condition." The British Journal of Dermatology, vol. 94, no. 3, 1976, pp. 277-89.
Hay RJ, Wells RS. The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition. Br J Dermatol. 1976;94(3):277-89.
Hay, R. J., & Wells, R. S. (1976). The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition. The British Journal of Dermatology, 94(3), 277-89.
Hay RJ, Wells RS. The Syndrome of Ankyloblepharon, Ectodermal Defects and Cleft Lip and Palate: an Autosomal Dominant Condition. Br J Dermatol. 1976;94(3):277-89. PubMed PMID: 946410.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition. AU - Hay,R J, AU - Wells,R S, PY - 1976/3/1/pubmed PY - 1976/3/1/medline PY - 1976/3/1/entrez SP - 277 EP - 89 JF - The British journal of dermatology JO - Br J Dermatol VL - 94 IS - 3 N2 - 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. SN - 0007-0963 UR - https://wwww.unboundmedicine.com/medline/citation/946410/The_syndrome_of_ankyloblepharon_ectodermal_defects_and_cleft_lip_and_palate:_an_autosomal_dominant_condition_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0007-0963&date=1976&volume=94&issue=3&spage=277 DB - PRIME DP - Unbound Medicine ER -