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Acrofacial dysostosis of unknown type: nosology of the acrofacial dysostoses.
Am J Med Genet. 1995 Mar 27; 56(2):155-60.AJ

Abstract

We describe a stillborn girl with an unclassified form of mandibulofacial dysostosis, a postaxial defect of the right, and a preaxial defect of the left hand. The Nager syndrome is characterized by preaxial limb defects, whereas the Genée-Wiedemann syndrome (= Miller syndrome) by postaxial limb defects. We briefly review the established acrofacial dysostoses (AFD) and discuss the position of our case in the current classification.

Authors+Show Affiliations

Department of Pediatrics, University of Düsseldorf, Germany.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Review

Language

eng

PubMed ID

7625437

Citation

Preis, S, et al. "Acrofacial Dysostosis of Unknown Type: Nosology of the Acrofacial Dysostoses." American Journal of Medical Genetics, vol. 56, no. 2, 1995, pp. 155-60.
Preis S, Raymaekers-Buntinx I, Majewski F. Acrofacial dysostosis of unknown type: nosology of the acrofacial dysostoses. Am J Med Genet. 1995;56(2):155-60.
Preis, S., Raymaekers-Buntinx, I., & Majewski, F. (1995). Acrofacial dysostosis of unknown type: nosology of the acrofacial dysostoses. American Journal of Medical Genetics, 56(2), 155-60.
Preis S, Raymaekers-Buntinx I, Majewski F. Acrofacial Dysostosis of Unknown Type: Nosology of the Acrofacial Dysostoses. Am J Med Genet. 1995 Mar 27;56(2):155-60. PubMed PMID: 7625437.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Acrofacial dysostosis of unknown type: nosology of the acrofacial dysostoses. AU - Preis,S, AU - Raymaekers-Buntinx,I, AU - Majewski,F, PY - 1995/3/27/pubmed PY - 1995/3/27/medline PY - 1995/3/27/entrez SP - 155 EP - 60 JF - American journal of medical genetics JO - Am J Med Genet VL - 56 IS - 2 N2 - We describe a stillborn girl with an unclassified form of mandibulofacial dysostosis, a postaxial defect of the right, and a preaxial defect of the left hand. The Nager syndrome is characterized by preaxial limb defects, whereas the Genée-Wiedemann syndrome (= Miller syndrome) by postaxial limb defects. We briefly review the established acrofacial dysostoses (AFD) and discuss the position of our case in the current classification. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/7625437/Acrofacial_dysostosis_of_unknown_type:_nosology_of_the_acrofacial_dysostoses_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1995&volume=56&issue=2&spage=155 DB - PRIME DP - Unbound Medicine ER -