Yuncheng People's Hospital
SMA

Treatment of SMA in Yuncheng

Yuncheng People's Hospital includes spinal muscular atrophy among the genetic developmental disorders treated by its rehabilitation department, combining physical therapy, occupational therapy, and equipment-based physiotherapy.

Стабилизация и сдвиг по моторным шкалам
improvement
patients
2–3 months
course
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About the condition

What is Spinal Muscular Atrophy (SMA)?

Spinal muscular atrophy (SMA) is a genetic neuromuscular disease that Yuncheng People's Hospital lists among the genetic developmental disorders treated by its pediatric neurology practice. For children with SMA, the clinic uses a broad range of modern equipment-based physiotherapy combined with physical therapy and occupational therapy.

What parents should know

Based on the experience of families who have completed rehabilitation at the clinic, progress with SMA develops gradually: improvements in head control, hand use, and rolling to the side become noticeable over several months of regular sessions.

Required examinations

Before the video consultation, it helps to provide a medical discharge summary with the diagnosis and, if available, genetic test results.

Causes

SMA is caused by a mutation in the SMN1 gene on chromosome 5 — in the vast majority of patients this is a deletion of exon 7. The SMN1 gene is responsible for producing a protein that motor neurons in the spinal cord need to function; when it is deficient, these neurons gradually die off, leading to muscle weakness. How severe the condition is largely depends on the number of copies of the 'backup' SMN2 gene — the more copies, the milder the disease tends to be. SMA is inherited in an autosomal recessive pattern, so both parents are usually healthy carriers.

Symptoms

Based on the clinic's description and patient experience, SMA presents with marked general weakness, difficulty holding the head up, limited hand movement, and chewing difficulties due to muscle weakness.

Diagnostics

Before the video consultation, the clinic needs a medical discharge summary with the diagnosis and case history; if available, genetic test results confirming the diagnosis.

Prognosis and Treatment Approach

The clinic classifies SMA among the neurological disorders treated with a broad range of equipment-based physiotherapy combined with PT and occupational therapy. Based on the clinic's patient experience, gradual progress in head control, hand use, and rolling to the side is possible over a course of treatment; the specific program and duration are determined individually.

Our approach

How we treat

01

Diagnostics

Comprehensive examination and patient assessment by an international team of specialists

02

Treatment plan

Development of an individual rehabilitation program considering diagnosis specifics

03

Therapy

Intensive course of procedures: physical therapy, massage, physiotherapy, acupuncture and other methods

04

Results

Progress evaluation, home recommendations and maintenance therapy plan

FAQ

Questions about treatment of Spinal Muscular Atrophy (SMA)

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