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Monosomy 10qter.

C Turleau·J de Grouchy·G Ponsot·D Bouygues
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Abstract

An 11-year-old girl with 10q26qter deletion is described and compared with another patient reported in the literature. The most characteristic features of monosomy 10qter seem to be: severe mental retardation; growth retardation; microcephaly; and facial dysmorphism with a long and triangular facies, a broad and prominent nasal bridge, a poorly developed tip of the nose, a short philtrum, and flattened angles of the mandible. Several of these features are opposed in type and countertype to features of trisomy 10qter.

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ChildChromosome DeletionChromosomes, Human, 6-12 and XFaceFemaleGrowth DisordersHumansIntellectual DisabilityMicrocephalySyndromeCase ReportsJournal Article

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BibTeXRIS

C Turleau, J de Grouchy, G Ponsot, D Bouygues. 1979-04-05. Monosomy 10qter.. https://doi.org/10.1007/bf00321014

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