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EEC syndrome: report on 20 new patients, clinical and genetic considerations.
Am J Med Genet. 1990 Sep; 37(1):42-53.AJ

Abstract

We report on 20 Brazilian patients (11 sporadic and 9 familial cases) with the ectrodactyly, ectodermal dysplasia, clefting syndrome (EEC syndrome). Genetic aspects, clinical manifestations, and differential diagnosis of the syndromes involving ectodermal dysplasia/limb anomalies and cleft lip/palate are discussed.

Authors+Show Affiliations

Laboratório de Genética Humana, Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, USP, Bauru, Brazil.No affiliation info available

Pub Type(s)

Case Reports
Journal Article
Review

Language

eng

PubMed ID

2240042

Citation

Rodini, E S., and A Richieri-Costa. "EEC Syndrome: Report On 20 New Patients, Clinical and Genetic Considerations." American Journal of Medical Genetics, vol. 37, no. 1, 1990, pp. 42-53.
Rodini ES, Richieri-Costa A. EEC syndrome: report on 20 new patients, clinical and genetic considerations. Am J Med Genet. 1990;37(1):42-53.
Rodini, E. S., & Richieri-Costa, A. (1990). EEC syndrome: report on 20 new patients, clinical and genetic considerations. American Journal of Medical Genetics, 37(1), 42-53.
Rodini ES, Richieri-Costa A. EEC Syndrome: Report On 20 New Patients, Clinical and Genetic Considerations. Am J Med Genet. 1990;37(1):42-53. PubMed PMID: 2240042.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - EEC syndrome: report on 20 new patients, clinical and genetic considerations. AU - Rodini,E S, AU - Richieri-Costa,A, PY - 1990/9/1/pubmed PY - 1990/9/1/medline PY - 1990/9/1/entrez SP - 42 EP - 53 JF - American journal of medical genetics JO - Am J Med Genet VL - 37 IS - 1 N2 - We report on 20 Brazilian patients (11 sporadic and 9 familial cases) with the ectrodactyly, ectodermal dysplasia, clefting syndrome (EEC syndrome). Genetic aspects, clinical manifestations, and differential diagnosis of the syndromes involving ectodermal dysplasia/limb anomalies and cleft lip/palate are discussed. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/2240042/EEC_syndrome:_report_on_20_new_patients_clinical_and_genetic_considerations_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1990&volume=37&issue=1&spage=42 DB - PRIME DP - Unbound Medicine ER -