Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 6 of 6 for MECP2 duplication syndrome
  1. MECP2 duplication syndrome is a condition that occurs almost exclusively in males and is characterized by moderate to severe intellectual disability. Most ...
  2. ... of the MECP2 gene in each cell causes MECP2 duplication syndrome, a condition characterized by intellectual disability, delayed development, ... brain activity, causing the signs and symptoms of MECP2 duplication syndrome. More About This Health Condition At least 19 ...
  3. ... disorders on the spectrum include PPM-X syndrome, MECP2 duplication syndrome, and MECP2-related severe neonatal encephalopathy. These other conditions can ...
  4. ... The mildest is PPM-X syndrome, followed by MECP2 duplication syndrome, then Rett syndrome (which exclusively affects females), and finally MECP2-related severe neonatal encephalopathy. MECP2-related severe neonatal ...
  5. Developmental Disabilities (National Library of Medicine)  
    Developmental disabilities are severe, long-term problems. They may be physical, such as blindness. They may affect mental ability, such as learning disabilities. ...
  6. What Causes Rett Syndrome? From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Rett Syndrome/Genetics ... Rett Syndrome ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes of Health