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Trader Willi syndrome with hypothyroidism
Author(s) -
BHATE M. S.,
ROBERTSON P. E.,
DAVISON E. V.,
BRUMMITT J. A.
Publication year - 1989
Publication title -
journal of intellectual disability research
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.941
H-Index - 104
eISSN - 1365-2788
pISSN - 0964-2633
DOI - 10.1111/j.1365-2788.1989.tb01471.x
Subject(s) - pediatrics , psychology , medicine , psychiatry
. 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,det(15Kq11.1q11.2) karyotype.