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Results 1 - 10 of 129 for Miller syndrome
  1. Miller syndrome 
    Miller syndrome is a rare condition that mainly affects the development of the face, arms, and legs. The ... disorder can vary among affected individuals.Individuals with Miller syndrome typically have facial differences, which can include underdeveloped ...
    https://medlineplus.gov/genetics/condition/miller-syndrome - Genetics
  2. Miller-Dieker syndrome 
    Miller-Dieker syndrome is a condition characterized by a pattern of abnormal brain development called lissencephaly. Normally, the surface of the brain (cerebral ...
    https://medlineplus.gov/genetics/condition/miller-dieker-syndrome - Genetics
  3. DHODH gene 
    ... the DHODH gene have been found to cause Miller syndrome, a rare condition that mainly affects the development ... and legs. Most of the variants that cause Miller syndrome change single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/dhodh - Genetics
  4. YWHAE gene 
    ... the short (p) arm of chromosome 17 causes Miller-Dieker syndrome. This region contains numerous genes, including the YWHAE gene. Miller-Dieker syndrome is characterized by intellectual disabilities and developmental delays ...
    https://medlineplus.gov/genetics/gene/ywhae - Genetics
  5. Chromosome 17 
    ... de Vries syndrome. More About This Health Condition Miller-Dieker syndrome is caused by a deletion of genetic material ... of the short (p) arm of chromosome 17. Miller-Dieker syndrome is a condition characterized by intellectual disabilities and ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  6. PAFAH1B1 gene 
    ... the short (p) arm of chromosome 17 causes Miller-Dieker syndrome. This region contains numerous genes, including the PAFAH1B1 gene. Signs and symptoms of Miller-Dieker syndrome include lissencephaly, intellectual disabilities, seizures, and distinctive facial ...
    https://medlineplus.gov/genetics/gene/pafah1b1 - Genetics
  7. Guillain-Barré syndrome 
    ... and can have abnormal or absent reflexes (areflexia).Miller Fisher syndrome, another type of Guillain-Barré syndrome, involves cranial ... to various areas of the head and neck. Miller Fisher syndrome is characterized by three features: weakness or paralysis ...
    https://medlineplus.gov/genetics/condition/guillain-barre-syndrome - Genetics
  8. Bone Diseases (National Library of Medicine)  
    Your bones help you move, give you shape and support your body. They are living tissues that rebuild constantly throughout your life. During childhood and ...
    https://medlineplus.gov/bonediseases.html - Health Topics
  9. Alagille syndrome 
    ... Hepatofacioneurocardiovertebral syndrome Paucity of interlobular bile ducts Watson-Miller syndrome Genetic Testing Registry: Alagille syndrome due to a ...
    https://medlineplus.gov/genetics/condition/alagille-syndrome - Genetics
  10. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
    https://medlineplus.gov/craniofacialabnormalities.html - Health Topics
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