脊髓性肌萎缩症（spinal muscular atrophy，SMA）是一种常染色体隐性遗传的神经肌肉疾病，主要是运动神经元存活基因1（survival motor neuron gene 1，SMN1 ...

（大山脚16日讯）6岁女童自出生后便被诊断患有罕见的脊髓性肌萎缩症（Spinal Muscular Atrophy Type 2，简称SMA Type ...

Newborn with SMA gene mutation receives presymptomatic treatment at SAT Hospital, a rare step in managing rare diseases.

A 'fragile' girl's life has been transformed thanks to "caring and loving" staff at a hospice. Ellie, 12, from Salisbury, ...

Spinal muscular atrophy (SMA) is a progressive neurodegenerative disorder set in motion before birth. Scientists at St. Jude Children's Research Hospital led the first in utero treatment of SMA ...

Spinal Muscular Atrophy treatment is evolving fast, with gene therapy, oral drugs, and next-gen muscle enhancers offering new hope and long-term outcomes. With each breakthrough in SMA treatment, we ...

But now there is a ray of light. Lilah is scheduled for surgery on July 15 that will see a metal ring called a halo fastened ...

The baby from Ranaghat in Nadia is suffering from spinal muscular atrophy (SMA) Type I, a condition that causes progressive ...

Thiruvananthapuram: For the first time in India, pre-symptomatic treatment to an infant, diagnosed with spinal muscular ...

A girl was diagnosed with a rare muscle -wasting condition after she stopped crawling as a baby. Ellie Soares, 11, seemed ...

Liu walks with an unsteady gait due to muscular atrophy in lower legs, she affectionately calls herself Waiwai, meaning ...