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Results 1 - 10 of 11 for Neurodevelopmental disorder with involuntary movements
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  1. GRIN2B-related neurodevelopmental disorder 
    ... unusually small head size (microcephaly), impaired vision, and involuntary muscle movements. The prevalence of GRIN2B-related neurodevelopmental disorder is unknown. Fewer than 100 cases have been ...
    https://medlineplus.gov/...rin2b-related-neurodevelopmental-disorder - Genetics
  2. CUL3-related neurodevelopmental disorder 
    ... can also occur in people with CUL3-related neurodevelopmental disorder. Affected ... (spasms). People with CUL3-related neurodevelopmental disorder can ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  3. CHD2 myoclonic encephalopathy 
    ... disorder in their family. CHD2 encephalopathy CHD2-related neurodevelopmental disorders Genetic Testing Registry: Developmental and epileptic encephalopathy 94 ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  4. ATN1 gene 
    ... Dentatorubral-pallidoluysian atrophy (DRPLA) is a progressive brain disorder that causes involuntary movements, mental and emotional problems, and a decline in ...
    https://medlineplus.gov/genetics/gene/atn1 - Genetics
  5. STXBP1 encephalopathy 
    ... KI. MUNC18-1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development. Acta ... JR, Moller RS, Weckhuysen S. STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy. Neurology. 2016 Mar 8;86(10): ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  6. DLG4-related synaptopathy 
    ... this condition cannot speak. Affected individuals often have neurodevelopmental disorders, such as autism spectrum disorder or attention-deficit/ ... PubMed Levy AM, Gomez-Puertas P, Tumer Z. Neurodevelopmental Disorders Associated with PSD-95 and Its Interaction Partners. ...
    https://medlineplus.gov/genetics/condition/dlg4-related-synaptopathy - Genetics
  7. SCN8A-related epilepsy with encephalopathy 
    ... M, Schreiber JM. SCN8A-Related Epilepsy and/or Neurodevelopmental Disorders. 2016 Aug 25 [updated 2023 Apr 6]. In: ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  8. 7q11.23 duplication syndrome 
    ... people with this disorder have above-average intelligence.Neurodevelopmental problems associated with this condition include anxiety disorders (such as social phobias and selective mutism, which ...
    https://medlineplus.gov/.../condition/7q1123-duplication-syndrome - Genetics
  9. Beta-propeller protein-associated neurodegeneration 
    ... such as using utensils. Affected individuals can have neurodevelopmental issues that are often compared to features of a disorder called Rett syndrome. These features include repeated hand ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  10. Boucher-Neuhäuser syndrome 
    ... syndrome can also have abnormal eye movements, including involuntary ... symptom of the disorder, but vision problems or delayed puberty can be ...
    https://medlineplus.gov/.../condition/boucher-neuhauser-syndrome - Genetics
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