Prader‐Willi syndrome and Robertsonian translocations involving chromosome 15
Anthony C. Casamassima, Lawrence R. Shapiro, Patrick L. Wilmot, Karen Berk Smith
Abstract
Anthony C. Casamassima, Lawrence R. Shapiro, Patrick L. Wilmot, Karen Berk Smith
Abstract
A case of Prader-Willi syndrome is presented in which high resolution chromosome analysis revealed not only a familial Robertsonian translocation [t(13q15q)], but also a del(15) (q11.2q13) of the chromosome 15 not involved in the translocation. While there have been numerous reports of Robertsonian translocations involving chromosome 15 in patients with Prader-Willi syndrome, in this case, the Robertsonian translocation was shown to be unrelated to the clinical findings.
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A case of Prader-Willi syndrome is presented in which high resolution chromosome analysis revealed not only a familial Robertsonian translocation [t(13q15q)], but also a del(15) (q11.2q13) of the chromosome 15 not involved in the translocation. While there have been numerous reports of Robertsonian translocations involving chromosome 15 in patients with Prader-Willi syndrome, in this case, the Robertsonian translocation was shown to be unrelated to the clinical findings.
Key concepts: Chromosomal translocation, Robertsonian translocation, Biology, Genetics, Chromosome, Chromosome 21, Karyotype, Gene