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Updated: Jul 7, 2026

FISH for Pre-implantation Genetic Diagnosis
Published on: February 23, 2011
A Y/15 translocation in a 45,X male with Prader-Willi syndrome
S Puvabanditsin1, E Garrow, S Razi
1Department of Pediatrics, Jersey City Medical Center, Jersey City, New Jersey 07302, USA. surasak1@aol.com
Abstract:
We report a male neonate with a 45 X karyotype; the long arm of a chromosome 15 was translocated onto the proximal long arm of the Y chromosome. Breakpoints were identified by in situ fluorescence hybridization (FISH) on the proximal 15q13 and Yq11.2. The derivative chromosome has no primary centromere. Clinical features were compatible with Prader-Willi syndrome. This is the first report case ofmonosomy 15q and Yq deletion with Prader-Willi syndrome.
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