De Novo Duplication of Chromosome 7 (q21.1-q32); Case Report and Review of the Literature
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25 août 2010
À propos de cet article
Publié en ligne: 25 août 2010
Pages: 35 - 37
DOI: https://doi.org/10.2478/v10034-010-0016-6
Mots clés
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Cytogenetic analysis of a 1-year-old boy with multiple congenital anomalies revealed partial duplication of the chromosome 7q21.2-q32 band region. His main features included: frontal bossing, small jaw, low-set ears, deep-set eyes, strabismus, drooping left upper eyelid, widely-spaced eyes, short nose, long philtrum, down-curved upper lip, camptodactyly and hypotonia.