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Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
Am J Med Genet. 1992 Sep 15; 44(2):136-7.AJ

Abstract

The Simpson-Golabi-Behmel syndrome is an X-linked condition characterized by pre- and postnatal overgrowth, "coarse" face, postaxial polydactyly, midline defects, and psychomotor development ranging from normal to mildly retarded. We report on an additional sporadic patient with novel manifestations, contributing to a more thorough delineation of this syndrome.

Authors+Show Affiliations

Gurrieri F
Istituto di Genetica Medica, Facoltà di Medicina e Chirurgia A. Gemelli, U.C.S.C., Roma, Italy.
Cappa M
No affiliation info available
Neri G
No affiliation info available

MeSH

Abnormalities, MultipleAdolescentCardiomyopathy, DilatedFaceGenetic LinkageGrowth DisordersHernia, DiaphragmaticHumansMaleNipplesSyndromeX Chromosome

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

1456280

Citation

Gurrieri, F, et al. "Further Delineation of the Simpson-Golabi-Behmel (SGB) Syndrome." American Journal of Medical Genetics, vol. 44, no. 2, 1992, pp. 136-7.
Gurrieri F, Cappa M, Neri G. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome. Am J Med Genet. 1992;44(2):136-7.
Gurrieri, F., Cappa, M., & Neri, G. (1992). Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome. American Journal of Medical Genetics, 44(2), 136-7.
Gurrieri F, Cappa M, Neri G. Further Delineation of the Simpson-Golabi-Behmel (SGB) Syndrome. Am J Med Genet. 1992 Sep 15;44(2):136-7. PubMed PMID: 1456280.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome. AU - Gurrieri,F, AU - Cappa,M, AU - Neri,G, PY - 1992/9/15/pubmed PY - 1992/9/15/medline PY - 1992/9/15/entrez SP - 136 EP - 7 JF - American journal of medical genetics JO - Am J Med Genet VL - 44 IS - 2 N2 - The Simpson-Golabi-Behmel syndrome is an X-linked condition characterized by pre- and postnatal overgrowth, "coarse" face, postaxial polydactyly, midline defects, and psychomotor development ranging from normal to mildly retarded. We report on an additional sporadic patient with novel manifestations, contributing to a more thorough delineation of this syndrome. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/1456280/Further_delineation_of_the_Simpson_Golabi_Behmel__SGB__syndrome_ DB - PRIME DP - Unbound Medicine ER -