| Literature DB >> 2213846 |
E K Pivnick1, M B Qumsiyeh, A T Tharapel, J B Summitt, R S Wilroy.
Abstract
Reciprocal translocations involving the short arm of acrocentric chromosomes can segregate to produce partial duplications without associated deletions. We present a case of an infant with a 46,XY,-15,+der(15),T(6;15)(q23;p12)pat chromosome complement. The infant had multiple congenital abnormalities including cranial anomalies, facial dysmorphism, anterior webbing of the neck, cardiac anomalies, and joint contractures. From a comparison of the infant's phenotype with 20 other patients with a similar duplication, it is evident that partial duplication of the long arm of chromosome 6 is a clinically diagnosable syndrome.Entities:
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Year: 1990 PMID: 2213846 PMCID: PMC1017204 DOI: 10.1136/jmg.27.8.523
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318