Cerebroatrophic Hyperammonemia

Cerebroatrophic Hyperammonemia

Article
Brain & Nerve
Kids' Zone
+3
Contributed byMaulik P. Purohit MD MPHMar 20, 2018

The topic Cerebroatrophic Hyperammonemia you are seeking is a synonym, or alternative name, or is closely related to the medical condition Rett Syndrome.

Quick Summary:

  • Rett Syndrome is a rare inherited disorder. In this congenital disorder the grey matter of the brain is affected. Some consider Rett Syndrome to be a severe form of autism
  • The brain has white matter and grey matter. The grey matter is an important component of the brain. It plays an important role in controlling the senses, muscles, including memory and emotions
  • Rett Syndrome is caused by mutation in specific genes. It almost only affects girls. The affected child is unable to perform useful and purposeful movements. They also experience difficulty in social interactions and are unable to communicate effectively
  • The signs and symptoms of Rett Syndrome are many and varied, since the central nervous system is affected. There are 4 stages of the signs and symptoms that begins with the early-onset stage and progresses to a late motor deterioration stage

Please find comprehensive information on Rett Syndrome regarding definition, distribution, risk factors, causes, signs & symptoms, diagnosis, complications, treatment, prevention, prognosis, and additional useful information HERE.

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Maulik P. Purohit MD MPH

Assistant Medical Director, Medical Editorial Board, DoveMed Team

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