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خبر راه اندازی سامانه ثبت بیماران مبتلا به آتروفی نخاعی – عضلانی

خبر راه اندازی سامانه ثبت بیماران مبتلا به آتروفی نخاعی – عضلانی در سایت دانشگاه شهید بهشتی بارگزاری شد برای دیدن متن کامل خبر به لینک زیر مراجعه کنید   https://sbmu.ac.ir/index.jsp?siteid=518&fkeyid=&siteid=518&pageid=42632&newsview=104965

Drug treatment for spinal muscular atrophy types II and III

https://pubmed.ncbi.nlm.nih.gov/32006461/ Abstract Background: Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor neuron 1 (SMN1) gene on chromosome 5, or a heterozygous deletion in combination with a (point) mutation in the second SMN1 allele. This results in degeneration of anterior horn cells, which leads to progressive muscle weakness. Children with […]

FDA Approves Oral Treatment for Spinal Muscular Atrophy

The U.S. Food and Drug Administration today approved Evrysdi (risdiplam) to treat patients two months of age and older with spinal muscular atrophy (SMA), a rare and often fatal genetic disease affecting muscle strength and movement. This is the second drug and the first oral drug approved to treat this disease. “Evrysdi is the first drug for […]