（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 ...

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

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

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

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

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 ...

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

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

Panelists discuss how insurance challenges impact spinal muscular atrophy (SMA) care, with prior authorizations becoming more ...

In combination with Eli Lilly’s tirzepatide, marketed as Zepbound for obesity, Scholar Rock’s monolonal antibody helped ...

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 ...

Jaipur: The life of 20-month-old Kartik hangs in balance. Diagnosed with spinal muscular atrophy (SMA), a rare and life-threatening neuromuscular dise.