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Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1)
J P Fryns1, A Kleczkowska, E Smeets
1Center for Human Genetics, University of Leuven, Belgium.
American Journal of Medical Genetics
|December 1, 1990
Abstract:
Here we report on a de novo apparently balanced reciprocal 5q;7p translocation in a 15-year-old girl with apparent Cohen syndrome characterized by hypotonia, obesity, multiple congenital anomalies, and mental retardation. This case may indicate that the gene for Cohen syndrome is at 5q33.1 or 7p15.1.