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ISSN: 2472-1115

Journal of Down Syndrome & Chromosome Abnormalities
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Prader-Willi Syndrome

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Prader-Willi Syndrome

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Prader-Willi Syndrome

Prader-Willi syndrome is a disorder caused by loss of genetic material from proximal arm of chromosome 15. An important characteristic of Prader-Willi syndrome is a continuous sense of hunger that usually begins at around 2 years of age. Persons with Prader-Willi syndrome want to eat constantly because they never feel full (hyperphagia) and usually have trouble controlling their weight. Many problems of Prader-Willi syndrome are due to obesity. The common features of this disease are mental retardation, short stature, small hands and small feet etc.

Related Journals of Prader-Willi Syndrome

Journal of Clinical & Medical Genomics, Cellular and Molecular Biology, Journal of Genetic Syndromes & Gene TherapyJournal of Tissue Science & EngineeringChromosome Research, Chromosome Research, Genes Chromosomes and Cancer, Genetics in Medicine, Human Genetics.

Prader-Willi Syndrome

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