Prader Willi syndrome with hypothyroidism

M S Bhate; P E Robertson; E V Davison; J A Brummitt

doi:10.1111/j.1365-2788.1989.tb01471.x

Prader Willi syndrome with hypothyroidism

J Ment Defic Res. 1989 Jun:33 ( Pt 3):235-44. doi: 10.1111/j.1365-2788.1989.tb01471.x.

Authors

M S Bhate¹, P E Robertson, E V Davison, J A Brummitt

Affiliation

¹ Prudhoe Hospital, Northumberland, England.

PMID: 2754723
DOI: 10.1111/j.1365-2788.1989.tb01471.x

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.

Publication types

Case Reports

MeSH terms

Adult
Child Development
Chromosome Deletion
Chromosomes, Human, Pair 15
Female
Humans
Hypothyroidism / genetics*
Intellectual Disability / genetics
Karyotyping
Obesity / genetics
Prader-Willi Syndrome / genetics*