டவுன் சிண்ட்ரோம் & குரோமோசோம் அசாதாரணங்களின் ஜர்னல்
திறந்த அணுகல்

சுருக்கம்

Genetic Disorder of Obesity and Intellectual Disability of Specific Genes in Prader-Willi Syndrome

Pinge Hui*

Prader-Willi condition is described by serious juvenile hypotonia with helpless suck and inability to flourish; hypogonadism causing genital hypoplasia and pubertal deficiency; trademark facial highlights; youth beginning heftiness and hyperphagia; formative deferral/gentle scholarly incapacity; short height; and a particular conduct aggregate. Rest irregularities and scoliosis are normal. Development chemical deficiency is continuous, and substitution treatment gives improvement in development, body organization, and actual traits. The board is generally to a great extent steady. Agreement clinical symptomatic measures exist, yet finding ought to be affirmed through hereditary testing. Prader-Willi disorder is because of nonattendance of in a fatherly way communicated engraved qualities at 15q11.2-q13 through fatherly cancellation of this area, maternal uniparental disomy 15 (2030%), or an engraving imperfection (13%). Parent-explicit DNA methylation investigation will distinguish >99% of people. Notwithstanding, extra hereditary investigations are important to distinguish the sub-atomic class. There are different engraved qualities around here, the deficiency of which add to the total aggregate of Prader-Willi condition. In any case, nonattendance of a little nucleolar arranging RNA quality, SNORD116, appears to repeat a considerable lot of the clinical highlights. Kin repeat hazard is regularly <1%, however higher dangers might relate in specific cases. Pre-birth finding is accessible.