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Apert Syndrome OMIM

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Location: http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=101200

Description: #101200 APERT SYNDROME
Alternative titles;
ACROCEPHALOSYNDACTYLY, TYPE I; ACS1
ACS I
APERT-CROUZON DISEASE, INCLUDED
ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED
ACS II, INCLUDED
VOGT CEPHALODACTYLY, INCLUDED
Apert syndrome is a congenital disorder characterized primarily by craniosynostosis, midface hypoplasia, and syndactyly of the hands and feet with a tendency to fusion of bony structures. Most cases are sporadic, but autosomal dominant inheritance has been reported

Type: Reference Material
Author/Contact: Victor A. McKusick
Institution: OMIM
Primary Subject/Category:

Language: English

Submitted by: admin
Hits: 203
Added: Sat Aug 08 2009
Last Modified: Fri Mar 05 2010