Global Rett Syndrome Market to Reach USD 70,797.27 thousand with a 75.6% CAGR
Rett syndrome is an uncommon neurological condition that affects mostly girls. Developmental difficulties, loss of motor abilities, and speech are all symptoms of the condition. Furthermore, the syndrome is diagnosed in children aged 6 to 18 months and is caused by mutations in the MECP2 gene on the X-chromosome. Rett syndrome can cause various problems, ranging from moderate to severe. Unusual eye movements, delayed growth, agitation and anger, poor language abilities, hand movement problems, muscular and coordination challenges, and breathing problems are all common symptoms of Rett syndrome.
Data Bridge Market Research analyses that the Rett syndrome market was valued at USD 783.11 thousand in 2021 and is expected to reach USD 70,797.27 thousand by 2029, registering a CAGR of 75.6% during the forecast period of 2022 to 2029. In addition to the market insights such as market value, growth rate, market segments, geographical coverage, market players, and market scenario, the market report curated by the Data Bridge Market Research team also includes in-depth expert analysis, patient epidemiology, pipeline analysis, pricing analysis, and regulatory framework.
Rett syndrome is rare neurological condition that primarily affects women. It is caused by a random gene mutation. Almost all patients require caregiver assistance throughout their lives. Many children with Rett syndrome reach adulthood with a high quality of life. Because there is no cure for Rett syndrome, treatment focuses on symptom management. The majority of afflicted children will benefit from occupational, physical, and speech treatment. Seizures, anxiety, sleep disorders, breathing problems, stereotypic hand movements, and certain gastrointestinal abnormalities are all signs of Rett syndrome that can be treated with drugs. Drugs can also help with muscular stiffness and spasticity.
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