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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Cite this paper

@article{Bhate1989PraderWS, title={Prader Willi syndrome with hypothyroidism.}, author={Manasi Bhate and Pat Robertson and Edwin Davison and J A Brummitt}, journal={Journal of mental deficiency research}, year={1989}, volume={33 ( Pt 3)}, pages={235-44} }