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Results 1 - 10 of 19 for Developmental delay seizures with or without movement abnormalities
  1. PIGN gene 
    ... seen in people with Fryns syndrome or MCAHS1 without having all of the features of these disorders. These individuals may have weak muscle tone (hypotonia), developmental delays, intellectual disabilities, movement disorders, and seizures. Researchers are working to learn more about the ...
    https://medlineplus.gov/genetics/gene/pign - Genetics
  2. Homocystinuria 
    ... are prone to fracture (osteoporosis) or other skeletal abnormalities. Some ... and problems with movement. They can also cause and a blood disorder ...
    https://medlineplus.gov/genetics/condition/homocystinuria - Genetics
  3. Deoxyguanosine kinase deficiency 
    ... include weak muscle tone (hypotonia), abnormal involuntary eye movements (nystagmus), developmental delays, and, rarely, seizures. Early signs of liver disease may include an ...
    https://medlineplus.gov/.../deoxyguanosine-kinase-deficiency - Genetics
  4. Epilepsy and Seizures From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Epilepsy/Start Here ... Epilepsy ... Seizures/Start Here ... Seizures ... National Institute of Neurological Disorders and Stroke ... Epilepsy is a chronic brain disorder in which ...
    https://www.ninds.nih.gov/.../disorders/epilepsy-and-seizures - External Health Links
  5. X-linked lissencephaly with abnormal genitalia 
    ... the brain (corpus callosum). In XLAG, the brain abnormalities can cause ... and recurrent seizures (epilepsy). Most children with XLAG do not survive ...
    https://medlineplus.gov/...ked-lissencephaly-with-abnormal-genitalia - Genetics
  6. Pediatric MRI Video (Radiological Society of North America) (American College of Radiology)  
    ... as persistent headaches, dizziness, weakness, blurry vision or seizures help ... or acquired abnormalities determine the condition of nerve tissue within the ...
    https://www.radiologyinfo.org/en/info/pediatric-mri - Videos
  7. Desmosterolosis 
    ... is characterized by neurological problems, such as brain abnormalities and developmental delay, and can also include other signs and symptoms.Children with desmosterolosis have delayed speech and motor skills (such as ... abnormalities in desmosterolosis include malformation of the tissue that ...
    https://medlineplus.gov/genetics/condition/desmosterolosis - Genetics
  8. Mitochondrial Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Muscle Disorders/Specifics ... Muscle Disorders
    https://www.ninds.nih.gov/.../disorders/mitochondrial-disorders - External Health Links
  9. MN1 C-terminal truncation syndrome 
    ... syndrome is a condition characterized by intellectual disability, developmental delay, distinctive facial features, and brain abnormalities.Most people with MCTT syndrome have mild to ...
    https://medlineplus.gov/.../mn1-c-terminal-truncation-syndrome - Genetics
  10. CUL3-related neurodevelopmental disorder 
    ... novo variants in CUL3 are associated with global developmental delays with or without infantile spasms. J Hum Genet. 2020 Sep;65( ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
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