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Results 11 - 20 of 91 for Palsy
  1. Alternating hemiplegia of childhood 
    ... neurological condition characterized by recurrent episodes of temporary paralysis, often affecting one side of the body (hemiplegia). During some episodes, the paralysis alternates from one side of the body to ...
    https://medlineplus.gov/.../alternating-hemiplegia-of-childhood - Genetics
  2. Moebius syndrome 
    ... this condition are present from birth.Weakness or paralysis of the facial muscles is one of the ... nerves leads to the facial muscle weakness or paralysis that is characteristic of Moebius syndrome.Researchers speculate ...
    https://medlineplus.gov/genetics/condition/moebius-syndrome - Genetics
  3. Ochoa syndrome 
    ... neuropathic bladder Inverted smile-neurogenic bladder Partial facial palsy with urinary abnormalities UFS Urofacial Ochoa's syndrome ...
    https://medlineplus.gov/genetics/condition/ochoa-syndrome - Genetics
  4. Myotonia congenita 
    Myotonia congenita is a disorder that affects muscles used for movement (skeletal muscles). Beginning in childhood, people with this condition experience bouts ...
    https://medlineplus.gov/genetics/condition/myotonia-congenita - Genetics
  5. MAPT gene 
    ... gene have been found to cause progressive supranuclear palsy. However, mutations in this gene appear to be ... with an increased risk of developing progressive supranuclear palsy. This polymorphism, known as the H1 haplotype, is ...
    https://medlineplus.gov/genetics/gene/mapt - Genetics
  6. SCN4A gene 
    ... gene have been found to cause hyperkalemic periodic paralysis, a condition that causes episodes of extreme muscle ... contract, leading to episodes of muscle weakness or paralysis. More About This Health Condition At least nine ...
    https://medlineplus.gov/genetics/gene/scn4a - Genetics
  7. ALS2 gene 
    ... found to cause infantile-onset ascending hereditary spastic paralysis. This disorder is characterized by progressive weakness and ... gene mutations cause infantile-onset ascending hereditary spastic paralysis. Research suggests that a lack of alsin and ...
    https://medlineplus.gov/genetics/gene/als2 - Genetics
  8. CACNA1S gene 
    ... have been identified in people with hypokalemic periodic paralysis, a condition that causes episodes of extreme muscle ... of muscle weakness in people with hypokalemic periodic paralysis. More About This Health Condition CAC1S_HUMAN CACH1 ...
    https://medlineplus.gov/genetics/gene/cacna1s - Genetics
  9. ROBO3 gene 
    ... have been identified in people with horizontal gaze palsy with progressive scoliosis (HGPPS). These mutations change the ... TM. Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations. J ...
    https://medlineplus.gov/genetics/gene/robo3 - Genetics
  10. Lattice corneal dystrophy type II 
    ... the head and face (cranial nerves) can cause paralysis of facial muscles (facial palsy); decreased sensations in the face (facial hypoesthesia); and ... and itchy. Because of loose skin and muscle paralysis in the face, individuals with lattice corneal dystrophy ...
    https://medlineplus.gov/.../lattice-corneal-dystrophy-type-ii - Genetics
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