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Dandy-Walker malformation and polydactyly: a possible expression of hydrolethalus syndrome.
Clin Genet. 1996 Apr; 49(4):211-5.CG

Abstract

Hydrolethalus syndrome consists of hydrocephalus, polydactyly, micrognathia, midcranial malformations, visceral abnormalities and perinatal lethality. It was first described in Finland, and only a few other cases outside Scandinavia are known. We report the first Hungarian patient who displayed many signs of the syndrome but had no cleft lip and visceral abnormalities. This observation suggests the existence of oligosymptomic hydrolethalus syndrome, and suggests that Dandy-Walker malformation with polydactyly may be a manifestation of the hydrolethalus syndrome.

Authors+Show Affiliations

Department of Pediatrics, University Medical School of Pécs, Hungary.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

8828988

Citation

Morava, E, et al. "Dandy-Walker Malformation and Polydactyly: a Possible Expression of Hydrolethalus Syndrome." Clinical Genetics, vol. 49, no. 4, 1996, pp. 211-5.
Morava E, Adamovich K, Czeizel AE. Dandy-Walker malformation and polydactyly: a possible expression of hydrolethalus syndrome. Clin Genet. 1996;49(4):211-5.
Morava, E., Adamovich, K., & Czeizel, A. E. (1996). Dandy-Walker malformation and polydactyly: a possible expression of hydrolethalus syndrome. Clinical Genetics, 49(4), 211-5.
Morava E, Adamovich K, Czeizel AE. Dandy-Walker Malformation and Polydactyly: a Possible Expression of Hydrolethalus Syndrome. Clin Genet. 1996;49(4):211-5. PubMed PMID: 8828988.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Dandy-Walker malformation and polydactyly: a possible expression of hydrolethalus syndrome. AU - Morava,E, AU - Adamovich,K, AU - Czeizel,A E, PY - 1996/4/1/pubmed PY - 2000/5/19/medline PY - 1996/4/1/entrez SP - 211 EP - 5 JF - Clinical genetics JO - Clin Genet VL - 49 IS - 4 N2 - Hydrolethalus syndrome consists of hydrocephalus, polydactyly, micrognathia, midcranial malformations, visceral abnormalities and perinatal lethality. It was first described in Finland, and only a few other cases outside Scandinavia are known. We report the first Hungarian patient who displayed many signs of the syndrome but had no cleft lip and visceral abnormalities. This observation suggests the existence of oligosymptomic hydrolethalus syndrome, and suggests that Dandy-Walker malformation with polydactyly may be a manifestation of the hydrolethalus syndrome. SN - 0009-9163 UR - https://www.unboundmedicine.com/medline/citation/8828988/Dandy_Walker_malformation_and_polydactyly:_a_possible_expression_of_hydrolethalus_syndrome_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0009-9163&date=1996&volume=49&issue=4&spage=211 DB - PRIME DP - Unbound Medicine ER -