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Results 1 - 10 of 15 for Intellectual "disability," progressive
  1. Mucopolysaccharidoses From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Carbohydrate Metabolism Disorders/Specifics ... Carbohydrate Metabolism Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes ...
    https://www.ninds.nih.gov/.../disorders/mucopolysaccharidoses - External Health Links
  2. Coffin-Lowry Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Facial Injuries and Disorders/Specifics ... Facial Injuries and Disorders ... Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... National Institute of ...
    https://www.ninds.nih.gov/.../disorders/coffin-lowry-syndrome - External Health Links
  3. Huntington Disease From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Huntington's Disease/Learn More ... Huntington's Disease ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and ...
    https://rarediseases.info.nih.gov/diseases/6677/huntington-disease - External Health Links
  4. Cerebellar Hypoplasia From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Specifics ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Cerebellar ...
    https://www.ninds.nih.gov/.../disorders/cerebellar-hypoplasia - External Health Links
  5. About Fragile X Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Fragile X syndrome is an inherited intellectual disability caused by a mutation in the FMR1 gene.
    https://www.genome.gov/Genetic-Disorders/Fragile-X-Syndrome - External Health Links
  6. Williams Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Genetic Disorders/Specifics ... Genetic Disorders ... Developmental Disabilities/Specifics ... Developmental Disabilities ... Genetic and Rare Diseases Information Center ...
    https://rarediseases.info.nih.gov/diseases/7891/williams-syndrome - External Health Links
  7. Cerebral Palsy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebral palsy (CP) refers to a group of neurological disorders that appear in infancy or early childhood and permanently affect body movement and muscle ...
    https://www.ninds.nih.gov/.../disorders/cerebral-palsy - External Health Links
  8. What Are the Symptoms of Rett Syndrome? From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    The first symptom of Rett syndrome is usually the loss of muscle tone, called hypotonia. With hypotonia, an infant's arms and legs will appear "floppy."
    https://www.nichd.nih.gov/health/topics/rett/conditioninfo/symptoms - External Health Links
  9. Talking Glossary of Genetic Terms From the National Institutes of Health (National Human Genome Research Institute)  
    Genes and Gene Therapy/Reference Desk ... Genes and Gene Therapy ... Genetic Testing/Reference Desk ... Genetic Testing ... Genetic Counseling/Reference Desk ... Genetic Counseling
    https://www.genome.gov/genetics-glossary - External Health Links
  10. Epilepsy and Seizures From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Epilepsy is a chronic brain disorder in which groups of nerve cells, or neurons, in the brain sometimes send the wrong signals and cause seizures. Epilepsy ( ...
    https://www.ninds.nih.gov/.../disorders/epilepsy-and-seizures - External Health Links
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