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Severe postaxial acrofacial dysostosis: an anatomic and angiographic study.
Am J Med Genet. 1990 Apr; 35(4):490-2.AJ

Abstract

We describe a severe case of postaxial acrofacial dysostosis syndrome [POADS] or Genée-Wiedemann syndrome in a stillborn female. The report includes an arteriographic and anatomic study of the limbs. Previously unreported findings such as hypoplasia of the femora, ossification defect of the ischium and pubis, bilobed tongue, and lung hypoplasia were noted. This case documents further variability in the POADS or Genée-Wiedemann syndrome.

Authors+Show Affiliations

Department of Pathology, La Paz Hospital, Madrid, Spain.No affiliation info available

Pub Type(s)

Case Reports
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

2333876

Citation

Rodríguez, J I., and J Palacios. "Severe Postaxial Acrofacial Dysostosis: an Anatomic and Angiographic Study." American Journal of Medical Genetics, vol. 35, no. 4, 1990, pp. 490-2.
Rodríguez JI, Palacios J. Severe postaxial acrofacial dysostosis: an anatomic and angiographic study. Am J Med Genet. 1990;35(4):490-2.
Rodríguez, J. I., & Palacios, J. (1990). Severe postaxial acrofacial dysostosis: an anatomic and angiographic study. American Journal of Medical Genetics, 35(4), 490-2.
Rodríguez JI, Palacios J. Severe Postaxial Acrofacial Dysostosis: an Anatomic and Angiographic Study. Am J Med Genet. 1990;35(4):490-2. PubMed PMID: 2333876.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Severe postaxial acrofacial dysostosis: an anatomic and angiographic study. AU - Rodríguez,J I, AU - Palacios,J, PY - 1990/4/1/pubmed PY - 1990/4/1/medline PY - 1990/4/1/entrez SP - 490 EP - 2 JF - American journal of medical genetics JO - Am J Med Genet VL - 35 IS - 4 N2 - We describe a severe case of postaxial acrofacial dysostosis syndrome [POADS] or Genée-Wiedemann syndrome in a stillborn female. The report includes an arteriographic and anatomic study of the limbs. Previously unreported findings such as hypoplasia of the femora, ossification defect of the ischium and pubis, bilobed tongue, and lung hypoplasia were noted. This case documents further variability in the POADS or Genée-Wiedemann syndrome. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/2333876/Severe_postaxial_acrofacial_dysostosis:_an_anatomic_and_angiographic_study_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1990&volume=35&issue=4&spage=490 DB - PRIME DP - Unbound Medicine ER -