Display Settings:

Format

Send to:

Choose Destination
Am J Med Genet. 1992 Sep 15;44(2):129-35.

Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature.

Author information

  • 1Department of Human Genetics, Medical College of Virginia/Virginia Commonwealth University, Richmond 23298-0033.

Abstract

Simpson-Golabi-Behmel Syndrome (SGBS), an X-linked encephalo-tropho-schisis syndrome described in fewer than a dozen families, is characterized by pre- and postnatal overgrowth, "coarse" face, minor facial anomalies and, in more severe cases, multiple congenital anomalies and mental retardation. We report on 2 brothers with overgrowth, macrocephaly, polydactyly, supernumerary nipples, and characteristic facial appearance. In addition, the propositus also had pulmonic stenosis and a cleft palate. The findings present in our patients are compared to those in the original patients and to those in patients described more recently. Despite the fact that our patients have most of the minor and several of the more severe malformations, they are not mentally retarded.

PMID:
1456279
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Loading ...
    Write to the Help Desk