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Terminal deletion of chromosome 10q and its clinical features
R Kogasaka1, T Morohoshi, Y Sawada
1Department of Pediatrics, Sunagawa City Medical Center, Japan.
Acta Paediatrica Japonica : Overseas Edition
|February 1, 1990
Abstract:
A male case with terminal deletion of chromosome 10q has growth retardation, craniofacial dysmorphism, congenital heart disease and other minor anomalies. The karyotypic formula is 46, XY, del (10), (q26.1----qter) by a high resolution G-banding staining. There are few differences in clinical features between our case and the previously reported cases.