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Case Reports
. 1998;9(3):191-4.

Further delineation of the KBG syndrome

K Devriendt  1 , M Holvoet, J P Fryns
Affiliations
  • PMID: 9777340
Case Reports

Further delineation of the KBG syndrome

K Devriendt et al. Genet Couns. 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.

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