Нейролайф · DCP China
SMA

SMA — where it's treated in the network

Most families arrive with the SMA diagnosis already confirmed and a drug already prescribed — nusinersen (Spinraza), Zolgensma or risdiplam (Evrysdi) — looking for who will take on the rehabilitation side. A network case manager will help compare clinics by SMA type (I–IV), the child's age, respiratory function and travel logistics, then schedule the course around the injection calendar.

8188+
patients
from 4 weeks + regular cycles
course
About the condition

What is Spinal Muscular Atrophy (SMA)?

Spinal muscular atrophy (SMA) is an inherited neuromuscular disease in which motor neurons in the anterior horns of the spinal cord gradually die, and the signal from the brain to the muscles no longer arrives in full. The cause is a fault in the SMN1 gene on chromosome 5; severity depends on the SMN2 backup gene copy number. ICD-10 codes it as G12.0 (SMA type I) across G12.0–G12.9. It occurs in 1 of every 6,000–10,000 newborns.

Families usually reach the network case manager with the SMA diagnosis already confirmed and a drug already prescribed — nusinersen (Spinraza), Zolgensma or risdiplam (Evrysdi) — looking for who will take on the rehabilitation side. The case manager will help compare clinics by SMA type (I–IV), the child's age and respiratory function. Details on causes, symptoms, diagnostics and the rehabilitation program are in the expandable blocks below.

Frequently asked questions

Frequently asked questions about Spinal Muscular Atrophy (SMA)

Is rehabilitation suitable for SMA type I?

Can rehabilitation be combined with Spinraza/Zolgensma?

Which network clinic suits SMA with severe scoliosis?

How often are rehabilitation courses needed?

Talk to a network coordinator

The coordinator reviews your documents and suggests matching clinics. We reply on Telegram and WhatsApp within an hour on workdays.

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