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]

16 images [ from 1 to 15 ]	1 2 next


Prader-Willi Syndrome	Prader-Willi Syndrome	Imprinting Mutations in Prader-Willi Syndrome
American Family Physician	American Family Physician	American Journal of Human Genetics


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	Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes
Arquivos de Neuro-Psiquiatria	Child's Doctor	Genetics and Molecular Biology


Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of 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 Medical Genetics	Journal of Neurology, Neurosurgery and Psychiatry	Journal of Neurology, Neurosurgery and Psychiatry


Enhanced activation of reward mediating prefrontal regions in response to food stimuli in Prader-Willi syndrome	Satiety dysfunction in Prader-Willi syndrome demonstrated by fMRI	Prader-Willi syndrome
Journal of Neurology, Neurosurgery and Psychiatry	Journal of Neurology, Neurosurgery and Psychiatry	Medical Genetics


Prader-Willi syndrome	Prader-Willi syndrome	Prader-Willi syndrome
Neuroneonatology	Neuroneonatology	Neuroneonatology

16 images [ from 1 to 15 ]	1 2 next

Search with keyword(s) And Or Wildcard = *


Print this page

Php programming by Robert Barbey Edited by Aldo Campana, November 3, 2009