Congenital myopathy with oculo-facial abnormalities (Marden-Walker syndrome)
- PMID: 1877612
- DOI: 10.1002/ajmg.1320390402
Congenital myopathy with oculo-facial abnormalities (Marden-Walker syndrome)
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.
Similar articles
-
Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.Birth Defects Orig Artic Ser. 1975;11(2):104-8. Birth Defects Orig Artic Ser. 1975. PMID: 1227520
-
A new autosomal recessive syndrome with Noonan-like phenotype, myopathy with congenital contractures and malignant hyperthermia.Birth Defects Orig Artic Ser. 1985;21(2):111-7. Birth Defects Orig Artic Ser. 1985. PMID: 4041573 No abstract available.
-
[Genetic-morphologic fatal syndromes. Cerebro-oculo-facioskeletal syndrome (Pena-Shokeir syndrome II)].Pathologe. 1993 Jul;14(4):219-20. Pathologe. 1993. PMID: 8367388 German. No abstract available.
-
Marden-Walker syndrome: a case report and a critical review of the literature.Clin Dysmorphol. 1993 Jul;2(3):211-9. Clin Dysmorphol. 1993. PMID: 7506965 Review.
-
King syndrome: a genetically heterogenous phenotype due to congenital myopathies.Am J Med Genet. 1992 Aug 1;43(6):954-6. doi: 10.1002/ajmg.1320430610. Am J Med Genet. 1992. PMID: 1415346 Review.
Cited by
-
Unusual manifestation of Marden-Walker syndrome.Indian J Hum Genet. 2012 May;18(2):256-8. doi: 10.4103/0971-6866.100798. Indian J Hum Genet. 2012. PMID: 23162309 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical