Complete monosomy mosaic of chromosome 21: case report and review of literature.

Abstract

Complete monosomy mosaic of chromosome 21 is a rare disorder. The syndromic features are highly variable. This study describes a girl of Mexican origin with complete monosomy 21 in mosaicism with novel findings, including cortical atrophy, macrostomia, pectum excavatum and immune deficiencies. Parental karyotypes were normal. FISH analysis with probes from 21q22.1-q22.2 region and centromere of X DNA probe was performed on peripheral blood lymphocytes whereas 21q22.1-q22.2 and 21q, 4p, 4q subtelomeric DNA probes were tested in fibroblasts. We propose that the monosomy 21 mosaicism is the cause of the survival of children with more than 4 months of age.

• Authors: Jaime Toral-Lopez, Luz Maria Gonzalez-Huerta, Sergio A Cuevas-Covarrubias
• Journal: Gene (Gene) Vol. 510 Issue 2 Pg. 175-9 (Dec 01 2012) ISSN: 1879-0038 [Electronic] Netherlands
• PMID: 22985727 (Publication Type: Case Reports, Journal Article, Review)
• Copyright: Copyright © 2012 Elsevier B.V. All rights reserved.

Topics

• Chromosomes, Human, Pair 21 (genetics)
• Female
• Humans
• In Situ Hybridization, Fluorescence
• Karyotype
• Lymphocytes (pathology)
• Monosomy (genetics, physiopathology)
• Mosaicism