Prader Willi Syndrome Peer Review Journals | Open Access Journals

Journal of Genetics and Genomes

ISSN: 2684-4567

Open Access

Prader Willi Syndrome Peer Review Journals

Prader-Willi syndrome (PWS) is a multi systemic systemic genetic disorder occurred due to absence of expression of genes on the maternally inherited chromosome. Many of the minor behaviors could help mostly in diagnosis and critical in management. PWS is an illustration of a genetic circumstances including genomic imprinting. During inception many PW child can exhibit a range of behavioral problems that become more observable in adolescence and adulthood and inhibit mostly with aspect of life. Early diagnosis of PWS allows for early mediation, usually through daily recombinant growth hormone doses which supports gradual growth and increased muscle weight. The syndrome is treated the most common genetic cause of obesity occurring in for every one child among 30,000 births. This journal gives open platform to explore new innovations, developments , recent studies, treatments in the form of articles, case reports, research papers, and many more.

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