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Results 1 - 7 of 7 for "Rett's" disorder
  1. ... loss of purposeful hand use syndrome Rett disorder Rett's disorder Rett's syndrome RTT Genetic Testing Registry: Rett ...
  2. STXBP1 encephalopathy is a condition characterized by abnormal brain function (encephalopathy) and intellectual disability. Most affected individuals also have ...
  3. ... was previously described as a congenital variant of Rett syndrome, which is a similar disorder of brain development. ... disability, and problems with communication and language. However, Rett syndrome is diagnosed almost exclusively in females, while FOXG1 ...
  4. ... was previously classified as an atypical form of Rett syndrome. These conditions have common features, including seizures, intellectual ... its genetic cause are distinct from those of Rett syndrome, and CDKL5 deficiency disorder is now considered a ...
  5. ... X syndrome, followed by MECP2 duplication syndrome, then Rett syndrome (which exclusively affects females), and finally MECP2-related ... related severe neonatal encephalopathy. Instead, they typically develop Rett syndrome, which has signs and symptoms that include intellectual ...
  6. ... often compared to features of a disorder called Rett syndrome. These features include repeated hand wringing or clasping ( ...
  7. ... linked mental retardation, syndromic 13 Genetic Testing Registry: Rett syndrome X-linked intellectual disability-psychosis-macroorchidism syndrome National ...