22 top medical experts on Microhydranencephaly across 3 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Microhydranencephaly: Microhydranencephaly is a developmental abnormality that affects the brain. Signs and symptoms may include extreme microcephaly , scalp rugae (a series of ridges), profound developmental delay and severe intellectual disability . Imaging studies of the brain generally reveal incomplete brain formation and severe hydrocephalus (accumulation of fluid in the brain). In most cases, the underlying cause is unknown. Rarely, the condition is caused by changes (mutations) in the NDE1 gene and is inherited in an autosomal recessive manner. Treatment is based on the signs and symptoms present in each person.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Hydranencephaly and microcephaly


  

        

                    


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