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PubMed · 7308236

Partial monosomy 10p syndrome.

J M Klep-de Pater·J B Bijlsma·F M Alkema
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Abstract

A 7 year-old girl is described with a de novo deletion of the short arm of chromosome 10 (qter p13:). The clinical features of: mental retardation, a large asymmetric head, antimongoloid slant, exophthalmos, epicanthus, ptosis, abnormal ears, pectus excavatum and widely spaced nipples are compared with those of five earlier reported cases with a deletion 10p. The data available suggest the existence of a clinically recognizable monosomy 10p syndrome.

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Abnormalities, MultipleChildChromosome AberrationsChromosome DeletionChromosomes, Human, 6-12 and XFemaleHumansIntellectual DisabilitySyndromeCase ReportsJournal Article

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BibTeXRIS

J M Klep-de Pater, J B Bijlsma, F M Alkema. 1981. Partial monosomy 10p syndrome.. https://doi.org/10.1007/bf00441326

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