Prader-Willi syndrome

15q12, 15q11-q13 GeneReviews Google OMIM Orphanet PubMed Who named it? Wikipedia

*Gene map locus 15q12, 15q11-q13

Labhart-Willi syndrome

PWS

Prader-Labhart-Willi syndrome

[Clinical features: diminished fetal activity; obesity; muscular hypotonia; mental retardation; short stature; hypogonadotropic hypogonadism; small hands and feet]

[Inheritance: isolated cases]


Imprinting Mutations in Prader-Willi Syndrome	A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect	A 3-year-old markedly obese boy with Prader-Willi syndrome
American Journal of Human Genetics	Arquivos de Neuro-Psiquiatria	Child's Doctor


Prader-Willi Syndrome	Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes	Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of Prader-Willi syndrome
eMedicine	Genetics and Molecular Biology	Journal of Medical Genetics


Enhanced activation of reward mediating prefrontal regions in response to food stimuli in Prader-Willi syndrome	Enhanced activation of reward mediating prefrontal regions in response to food stimuli in Prader-Willi syndrome	Enhanced activation of reward mediating prefrontal regions in response to food stimuli in Prader-Willi syndrome
Journal of Neurology, Neurosurgery and Psychiatry	Journal of Neurology, Neurosurgery and Psychiatry	Journal of Neurology, Neurosurgery and Psychiatry


Satiety dysfunction in Prader-Willi syndrome demonstrated by fMRI	Prader-Willi syndrome	Prader-Willi syndrome
Journal of Neurology, Neurosurgery and Psychiatry	Medical Genetics	Neuroneonatology


Prader-Willi syndrome	Prader-Willi syndrome	Brain Developmental Abnormalities in Prader-Willi Syndrome Detected by Diffusion Tensor Imaging
Neuroneonatology	Neuroneonatology	Pediatrics

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Edited by Aldo Campana, February 8, 2010