SMA-005

Spinal Muscular Atrophy Type II (SMA-II)

Europe 18 months male Germany Total Cost: 958

Patient Condition

The child was diagnosed with SMA-II type at 6 months old, with a homozygous deletion of exon 7 of the SMN1 gene and a copy number of SMN2 was 3. The child was 2 years old when he came for treatment. He could sit alone but could not walk independently and needed assistive devices. The CHOP INTEND score is 42 and the HFMSE score is 28. Respiratory function: FVC 65% predicted, occasional decrease in nocturnal oxygen saturation (minimum 88%). Cobb angle of scoliosis is 15 degrees. Previously undergoing physical therapy and spinal brace therapy, motor function progressed slowly.

Treatment Timeline

PhaseDetailsDate
Comprehensive evaluation and treatment plan formulation
Spinraza loading dose therapy
Maintenance treatment and rehabilitation intensification
Long-term maintenance and functional optimization

Treatment Outcome

beforeHFMSE 28, sitting alone but not walking, FVC 65%, scoliosis 15 degrees, slow progress in motor function
afterHFMSE 45 points, walking assistance for 50 meters, FVC maintained at 70%, no progression of scoliosis, and significant improvement in self-care ability
highlightSpinraza treatment increased motor function scores in children with SMA-II by 61%, achieved assisted walking, and significantly improved quality of life