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Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome
1Istituto di Genetica Medica, Facoltà di Medicina e Chirurgia A. Gemelli, U.C.S.C., Roma, Italy.
American Journal of Medical Genetics
|September 15, 1992
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.