A Y/15 translocation in a 45,X male with Prader-Willi syndrome.

Journal: Genetic Counseling (Geneva, Switzerland)
Published:
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.

Authors
S Puvabanditsin, E Garrow, S Razi, A Mohar, J Tadros, N Phattraprayoon, P Patel