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ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
Am J Med Genet. 1993 Mar 01; 45(5):642-8.AJ

Abstract

We describe a family with at least seven living persons who are affected by an hitherto undescribed autosomal-dominant syndrome with variable expression, bearing close resemblance to the EEC syndrome and related disorders. The main manifestations are hypodontia and/or early loss of permanent teeth, ectrodactyly, obstruction of lacrimal ducts, onychodysplasia, and excessive freckling. We propose the acronym ADULT (acro-dermato-ungual-lacrimal-tooth)-syndrome for this condition.

Authors+Show Affiliations

Institut für Humangenetik, Universität Bonn, Germany.No affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

8456838

Citation

Propping, P, and K Zerres. "ADULT-syndrome: an Autosomal-dominant Disorder With Pigment Anomalies, Ectrodactyly, Nail Dysplasia, and Hypodontia." American Journal of Medical Genetics, vol. 45, no. 5, 1993, pp. 642-8.
Propping P, Zerres K. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia. Am J Med Genet. 1993;45(5):642-8.
Propping, P., & Zerres, K. (1993). ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia. American Journal of Medical Genetics, 45(5), 642-8.
Propping P, Zerres K. ADULT-syndrome: an Autosomal-dominant Disorder With Pigment Anomalies, Ectrodactyly, Nail Dysplasia, and Hypodontia. Am J Med Genet. 1993 Mar 1;45(5):642-8. PubMed PMID: 8456838.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia. AU - Propping,P, AU - Zerres,K, PY - 1993/3/1/pubmed PY - 1993/3/1/medline PY - 1993/3/1/entrez SP - 642 EP - 8 JF - American journal of medical genetics JO - Am. J. Med. Genet. VL - 45 IS - 5 N2 - We describe a family with at least seven living persons who are affected by an hitherto undescribed autosomal-dominant syndrome with variable expression, bearing close resemblance to the EEC syndrome and related disorders. The main manifestations are hypodontia and/or early loss of permanent teeth, ectrodactyly, obstruction of lacrimal ducts, onychodysplasia, and excessive freckling. We propose the acronym ADULT (acro-dermato-ungual-lacrimal-tooth)-syndrome for this condition. SN - 0148-7299 UR - https://wwww.unboundmedicine.com/medline/citation/8456838/ADULT_syndrome:_an_autosomal_dominant_disorder_with_pigment_anomalies_ectrodactyly_nail_dysplasia_and_hypodontia_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1993&volume=45&issue=5&spage=642 DB - PRIME DP - Unbound Medicine ER -