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Clinical Findings Associated with a De Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis

We present the case of an 18-month-old boy with dysmorphic facial features, developmental delay, growth retardation, bilateral clubfeet, thrombocytopenia, and strabismus, whose array CGH analysis revealed concurrent de novo trisomy 10p11.22p15.3 and monosomy 7p22.3. We describe the patient's cl...

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Main Authors: Omid Kohannim, Jane Peredo, Katrina M. Dipple, Fabiola Quintero-Rivera
Formato: Artigo
Idioma:Inglês
Publicado: Hindawi Limited 2011-01-01
Series:Case Reports in Genetics
Acceso en liña:http://dx.doi.org/10.1155/2011/131768
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