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Genet Couns. 1998;9(3):191-4.

Further delineation of the KBG syndrome.

Author information

1
Center for Human Genetics, University Hospital Leuven, Belgium.

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.

PMID:
9777340
[Indexed for MEDLINE]

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