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Results 11 - 18 of 18 for Impaired pain sensation
  1. Yuan-Harel-Lupski syndrome 
    ... of the PMP22 gene develop muscle weakness and impaired sensitivity to touch, heat, and cold. Duplications that ...
    https://medlineplus.gov/.../condition/yuan-harel-lupski-syndrome - Genetics
  2. Charcot-Marie-Tooth disease 
    ... RECESSIVE NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND ABSENT SENSORY LARGE MYELINATED FIBERS ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  3. Leprosy 
    ... to vision loss, destruction of nasal tissue, or impaired speech. Some affected individuals have damage to internal ... on the skin. There is generally loss of sensation in these areas, but the ... reactions, which involve pain and swelling of the skin lesions and the ...
    https://medlineplus.gov/genetics/condition/leprosy - Genetics
  4. Spastic paraplegia type 15 
    ... spastizin protein interferes with normal cytokinesis and whether impaired cell division contributes to the signs and symptoms ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-15 - Genetics
  5. Spastic paraplegia type 7 
    ... swelling of the cell, reduced cell signaling, and impaired cell movement, leading to the major signs and ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
  6. Hereditary neuralgic amyotrophy 
    ... with residual problems, such as chronic pain and impaired movement, that accumulate over time.Typically, an attack ... month. It may be difficult to control the pain with medication. Over a period of a ... sensation (hypoesthesia) and abnormal sensations in the skin such ...
    https://medlineplus.gov/.../hereditary-neuralgic-amyotrophy - Genetics
  7. Chronic atrial and intestinal dysrhythmia 
    ... diarrhea. Affected individuals experience loss of appetite and impaired ability to absorb nutrients, which may lead to ...
    https://medlineplus.gov/...chronic-atrial-and-intestinal-dysrhythmia - Genetics
  8. Alpha-N-acetylgalactosaminidase deficiency 
    ... in childhood. Autism spectrum disorder is characterized by impaired communication and socialization skills. People with type III ...
    https://medlineplus.gov/...lpha-n-acetylgalactosaminidase-deficiency - Genetics
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