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Further delineation of the KBG syndrome
K Devriendt1, M Holvoet, J P Fryns
1Center for Human Genetics, University Hospital Leuven, Belgium.
Genetic Counseling (Geneva, Switzerland)
|October 20, 1998
Abstract:
Further Delineation of the KBG syndrome: We present a mother and her daughter with clinical features of KBG syndrome, including mild mental retardation, distinct facial features, macrodontia and skeletal anomalies. In the daughter, a heart defect (ventricular septal defect) was present.