An interstitial deletion of the long arm of chromosome 13
- 1 April 1989
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 35 (4) , 276-281
- https://doi.org/10.1111/j.1399-0004.1989.tb02943.x
Abstract
A case of an interstitial deletion of chromosome 13, identified as 46,XY,del(13)(q22q31), is reported in a child with psychomotor retardation, prominent low-set ears, epicanthus, hypertelorism, broad nasal bridge, hypoplastic fifth fingers and abnormal dermatoglyphics. This patient is compared to others in the literature with a similar deletion.Keywords
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