Angelman Syndrome

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Angelman syndrome is a rare genetic condition caused by deficient gene expression of E3 ubiquitin protein ligase (also known as UBE3A) and was first described in 1965 by Dr Harry Angelman. Characteristic findings of Angelman syndrome include severe developmental delay and movement or balance disorder, usually in the form of gait ataxia and/or tremulous movement of limbs

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شكرا جزيلا لك على المعلومات القيمة
وعلى وجود الترجمة للغة العربية

szmcydc
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Sir kindly start making vedios again ...I'm preparing for my MBBS test and I'm addicted to your way of teaching....your sincere student from Pakistan 🇵🇰 ❤❤..Have a good life my Sir..

KamranUllah-uwht
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Saw colin farrels child has this, sad. Thank you

IQ-nvbm
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Thank you. I didn’t make about this disease

john.the.beloved