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Sylvian fissure morphology in Prader-Willi syndrome and early-onset morbid obesity
Author(s) -
Jennifer Miller,
Jessica A. Couch,
Christiana M. Leonard,
Krista Schwenk,
Stephen Towler,
Jonathan J. Shuster,
Anthony P. Goldstone,
Guojun He,
Daniel J. Driscoll,
Yijun Liu
Publication year - 2007
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1097/gim.0b013e31812f720d
Subject(s) - insula , psychology , operculum (bryozoa) , etiology , obesity , developmental psychology , audiology , medicine , neuroscience , psychiatry , biology , botany , genus
Prader-Willi syndrome is a well-defined genetic cause of childhood-onset obesity that can serve as a model for investigating early-onset childhood obesity. Individuals with Prader-Willi syndrome have speech and language impairments, suggesting possible involvement of the perisylvian region of the brain. Clinical observations suggest that many individuals with early-onset morbid obesity have similar speech/language deficits, indicating possible perisylvian involvement in these children as well. We hypothesized that similar perisylvian abnormalities may exist in both disorders.

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