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Congenital myopathy with oculo-facial abnormalities (Marden-Walker syndrome).
Am J Med Genet. 1991 Jun 15; 39(4):377-9.AJ

Abstract

Marden-Walker syndrome present in the neonatal period is characterized by oculo-facial abnormalities, congenital myopathy, and contractures. A newborn infant with a similar pattern of anomalies is reported, and further evidence for autosomal recessive inheritance as well as new neuropathological findings are included.

Authors+Show Affiliations

Department of Pediatrics, Hebrew University, Jerusalem, Israel.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

1877612

Citation

Linder, N, et al. "Congenital Myopathy With Oculo-facial Abnormalities (Marden-Walker Syndrome)." American Journal of Medical Genetics, vol. 39, no. 4, 1991, pp. 377-9.
Linder N, Mathot I, Livoff A, et al. Congenital myopathy with oculo-facial abnormalities (Marden-Walker syndrome). Am J Med Genet. 1991;39(4):377-9.
Linder, N., Mathot, I., Livoff, A., Glass, J., Bornstein, I., Gross, E., Yatsiv, S., & Sommer, A. (1991). Congenital myopathy with oculo-facial abnormalities (Marden-Walker syndrome). American Journal of Medical Genetics, 39(4), 377-9.
Linder N, et al. Congenital Myopathy With Oculo-facial Abnormalities (Marden-Walker Syndrome). Am J Med Genet. 1991 Jun 15;39(4):377-9. PubMed PMID: 1877612.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Congenital myopathy with oculo-facial abnormalities (Marden-Walker syndrome). AU - Linder,N, AU - Mathot,I, AU - Livoff,A, AU - Glass,J, AU - Bornstein,I, AU - Gross,E, AU - Yatsiv,S, AU - Sommer,A, PY - 1991/6/15/pubmed PY - 1991/6/15/medline PY - 1991/6/15/entrez SP - 377 EP - 9 JF - American journal of medical genetics JO - Am J Med Genet VL - 39 IS - 4 N2 - Marden-Walker syndrome present in the neonatal period is characterized by oculo-facial abnormalities, congenital myopathy, and contractures. A newborn infant with a similar pattern of anomalies is reported, and further evidence for autosomal recessive inheritance as well as new neuropathological findings are included. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/1877612/Congenital_myopathy_with_oculo_facial_abnormalities__Marden_Walker_syndrome__ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1991&volume=39&issue=4&spage=377 DB - PRIME DP - Unbound Medicine ER -