Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.

AUTOR(ES)

Glass, I A

RESUMO

We report a 16 year old boy with the abnormal karyotype 46,XY,del(2)(q32.2q33.1) who has mental retardation, microcephaly, epilepsy, craniofacial dysmorphism, distinctive scalloped skin pigmentation, and normal levels of isocitrate dehydrogenase.

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