Genetic — where it's treated in the network
Genetic conditions require a special approach focused on improving quality of life and maintaining body functions. Network coordinators help select the clinic and course format for children with spinal muscular atrophy (SMA), Duchenne muscular dystrophy (DMD), genetic epilepsy, Down syndrome, Friedreich's ataxia, and metachromatic leukodystrophy.
Where it is treated in our network
4 clinics in our network offer different approaches to this diagnosis.
- Shenzhen, China
Microbiota Lab
Gut-brain axis program as baseline for genetic diagnoses with GI comorbidities (especially Down syndrome — 40-50% with microbiome dysbiosis). Metagenomic 16S rRNA sequencing + personalized probiotics, nutraceuticals, FMT when indicated. As part of a multimodal plan with core rehabilitation.
Visit clinic site - Huizhou, China
Neurolife — Huizhou
Multidisciplinary program for all 6 genetic diagnoses: SMA I-IV, DMD, Down syndrome, Friedreich, leukodystrophies, genetic epilepsies. Coordination with the treating neurologist on disease-modifying therapy protocols (nusinersen/Zolgensma/Evrysdi/Spinraza), parallel rehabilitation with TCM adjuncts for immunity support.
Visit clinic site - Shangrao, China
Hansi — Stem Cells
Partner cell therapy center for selected candidates: autologous stem cells, perinatal cells, and exosome nasal therapy for neuroregeneration. Applicable for SMA, DMD, Down syndrome, Friedreich, leukodystrophies. 5-stage protocol with consultation+screening to determine responsiveness.
Visit clinic site - Tashkent, Uzbekistan
Neurolife — Tashkent
Basic support program without travelling to China: specialized exercise therapy, respiratory gymnastics, occupational therapy, speech therapy, psychologist-defectologist. For all SMA types, DMD, Down syndrome — outpatient observation between visits to Chinese clinics, coordination with parents on the course schedule in core network clinics.
Visit clinic site
What is Genetic Conditions?
Genetic conditions in pediatric rehabilitation form a broad group of diagnoses caused by DNA mutations. In most cases the diagnosis is already confirmed; the home neurologist has prescribed a drug (when one exists), and the family is looking for who will take on the rehabilitation side. ICD-10 covers several rubrics: G12 (SMA), G71 (muscular dystrophies), Q90 (Down syndrome), G11.1, E75.2.
Families reach the network case manager by specific diagnosis: SMA on nusinersen, Zolgensma or Evrysdi; Duchenne muscular dystrophy; Down syndrome and early intervention; Friedreich's ataxia; leukodystrophy. Dedicated pages for each diagnosis and a list of network clinics are below. Details on causes, symptoms and realistic outlook are in the expandable blocks.
Directions within this category
Each direction is a dedicated page covering the diagnosis and the network's approaches.
Frequently asked questions about Genetic Conditions
Can a genetic condition be cured?
Can rehabilitation be combined with gene therapy?
Which network clinic is right for my case?
What to do between rehabilitation courses?
How many times per year should one return for a course?
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.