Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1991 May;28(5):297-303.
doi: 10.1136/jmg.28.5.297.

Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study

Affiliations
Review

Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study

A Verloes et al. J Med Genet. 1991 May.

Abstract

A syndrome of holoprosencephaly and postaxial polydactyly, associated with hydrocephalus, heart defect, adrenal hypoplasia, and other visceral malformations, has been observed in five unrelated children with normal chromosomes. Clinical overlap with lethal acrodysgenital dwarfism (Smith-Lemli-Opitz syndrome type II) and hydrolethalus syndrome is discussed. Recessive inheritance seems likely.

PubMed Disclaimer

References

    1. J Med Genet. 1990 Dec;27(12):756-9 - PubMed
    1. Birth Defects Orig Artic Ser. 1975;11(2):294-313 - PubMed
    1. J Med Genet. 1988 Jul;25(7):501-2 - PubMed
    1. J Med Genet. 1988 Feb;25(2):88-95 - PubMed
    1. Am J Med Genet. 1989 Aug;33(4):489-99 - PubMed

MeSH terms