Format

Send to

Choose Destination
Clin Dysmorphol. 2000 Apr;9(2):87-91.

The KBG syndrome.

Author information

1
Department of Clinical Genetics, Institute of Child Health, Bristol Children's Hospital, UK.

Abstract

We report on two boys with a combination of short stature, a broad face, macrodontia and developmental delay. These features suggest that they have the KBG syndrome, a rare but distinctive phenotype. The pattern of inheritance remains uncertain and both autosomal dominant and X-linked recessive inheritance should be considered in genetic counselling.

PMID:
10826617
[Indexed for MEDLINE]

Supplemental Content

Loading ...
Support Center