Prader Willi syndrome with hypothyroidism
- PMID: 2754723
- DOI: 10.1111/j.1365-2788.1989.tb01471.x
Prader Willi syndrome with hypothyroidism
Abstract
A case of Prader Willi Syndrome who suffered from hypothyroidism is described. This patient on cytogenetic examination was found to have Mosaic 46,XX/46,XX,del(15)(q11.1q11.2) karyotype.
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