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.
Links
MeSH
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 -