TRISOMY 10P

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  • 1 January 1976
    • journal article
    • research article
    • Vol. 19  (1) , 57-60
Abstract
A stillborn male fetus having a trisomy of the short arm of chromosome 10 is described. The father is a carrier of the reciprocal translocation 46XY,t(10;21)(10pter.fwdarw.10p11: :21p11.fwdarw.21qter). The clinical picture included growth retardation, bilateral cleft lip and palate, micrognathia, short neck, microphalus and bilateral clubbed feet. The long bones were markedly thinned with spontaneous fractures. Autopsy findings included pulmonary hypoplasia and renal dyplasia. Previous reports of trisomy 10 and trisomy of the short arm of chromosome 10 are discussed.

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