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Results 41 - 50 of 64 for Autism spectrum disorder -epilepsy -arthrogryposis syndrome
  1. Rett syndrome 
    ... mutation are on the milder end of the spectrum. Autism-dementia-ataxia-loss of purposeful hand use syndrome Rett disorder Rett's disorder Rett's syndrome RTT Genetic ...
    https://medlineplus.gov/genetics/condition/rett-syndrome - Genetics
  2. Cowden syndrome 
    ... affected individuals have delayed development, intellectual disability, or autism spectrum disorder, which can affect communication and social interaction.Some people do not meet the strict criteria for a clinical diagnosis of Cowden syndrome, but they have some of the characteristic features ...
    https://medlineplus.gov/genetics/condition/cowden-syndrome - Genetics
  3. 2q37 deletion syndrome 
    ... 25 percent of people with this condition have autism spectrum disorder, a developmental condition that affects communication and social interaction.Unusual physical features are also common in people with 2q37 deletion syndrome. About half of affected individuals have unusually short ...
    https://medlineplus.gov/genetics/condition/2q37-deletion-syndrome - Genetics
  4. RAI1 gene 
    ... many of the major features of Potocki-Lupski syndrome. This condition is characterized by delayed development, mild to moderate intellectual disability, autism spectrum disorder (which affects social interaction and communication), sleep disturbances, ...
    https://medlineplus.gov/genetics/gene/rai1 - Genetics
  5. SHANK3 gene 
    ... speech characteristic of people with 22q13.3 deletion syndrome. More About This Health Condition At least 43 SHANK3 gene mutations have been found in people who have autism spectrum disorder (ASD), which is a varied condition characterized by ...
    https://medlineplus.gov/genetics/gene/shank3 - Genetics
  6. CTNND2 gene 
    ... function of synapses. MedlinePlus Genetics provides information about Autism spectrum disorder More About This Health Condition The CTNND2 gene is located in a region of chromosome 5 that is often deleted in people with cri-du-chat syndrome. As a result of this deletion, many people ...
    https://medlineplus.gov/genetics/gene/ctnnd2 - Genetics
  7. Distal 18q deletion syndrome 
    ... as anxiety, irritability, and depression; and features of autism spectrum disorder that affect ... Distal 18q deletion syndrome is caused by a ...
    https://medlineplus.gov/.../condition/distal-18q-deletion-syndrome - Genetics
  8. ARID1B gene 
    ... of Coffin-Siris syndrome. People with Coffin-Siris syndrome do not appear to have an ... autism spectrum disorder (ASD), a varied condition characterized by impaired social ...
    https://medlineplus.gov/genetics/gene/arid1b - Genetics
  9. POGZ gene 
    ... mutations have been found to cause White-Sutton syndrome. This disorder is ... spectrum disorder (ASD), a varied condition characterized by impaired ...
    https://medlineplus.gov/genetics/gene/pogz - Genetics
  10. 22q11.2 duplication 
    ... Portnoi MF. Microduplication 22q11.2: a new chromosomal syndrome. Eur J Med ... autism spectrum disorder: clinical and genetic study. Dev Med Child Neurol. ...
    https://medlineplus.gov/genetics/condition/22q112-duplication - Genetics
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