Biology, asked by yuvikajauhari5239, 10 months ago

Type of germlayer defect in prader willi syndrom

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Answered by sriharshab

Answer:

Prader-Willi syndrome (PWS) is a genetic syndrome caused by the lack of expression of imprinted genes located on paternal chromosome, characterized by endocrine defects, an insatiable appetite, short stature, cognitive and behavioral difficulties and dysmorphic features.

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