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Results 1 - 10 of 1,226 for mays
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  1. Alpha-1 antitrypsin deficiency 
    ... 1 antitrypsin deficiency is an inherited disorder that may cause lung disease and liver disease. The signs ... means that two different versions of the gene may be active (expressed), and both versions contribute to ...
    https://medlineplus.gov/.../condition/alpha-1-antitrypsin-deficiency - Genetics
  2. Paroxysmal nocturnal hemoglobinuria 
    ... sudden, recurring episodes of symptoms (paroxysmal symptoms), which may be triggered by stresses on the body, such ... earlier than they should be (hemolysis). Affected individuals may pass dark-colored urine because of the presence ...
    https://medlineplus.gov/.../paroxysmal-nocturnal-hemoglobinuria - Genetics
  3. Craniofacial microsomia 
    ... speech. In cases of severe mandibular hypoplasia, breathing may also be affected.People with craniofacial microsomia usually ... or both ears, typically to different degrees. They may have growths of skin (skin tags) in front ...
    https://medlineplus.gov/genetics/condition/craniofacial-microsomia - Genetics
  4. Systemic lupus erythematosus 
    ... the body's own tissues and organs.SLE may first appear as extreme tiredness (fatigue), a vague ... when exposed to sunlight. Other skin problems that may occur in SLE include calcium deposits under the ...
    https://medlineplus.gov/.../condition/systemic-lupus-erythematosus - Genetics
  5. Popliteal pterygium syndrome 
    ... roof of the mouth), or both. Affected individuals may have depressions (pits) near the center of the lower lip, which may appear moist due to the presence of salivary ...
    https://medlineplus.gov/.../condition/popliteal-pterygium-syndrome - Genetics
  6. Leukoencephalopathy with vanishing white matter 
    ... symptoms of the disorder at birth. Affected children may have slightly delayed development of motor skills such ... spasticity) and difficulty with coordinating movements (ataxia). There may also be some deterioration of mental functioning, but ...
    https://medlineplus.gov/...ncephalopathy-with-vanishing-white-matter - Genetics
  7. Early-onset isolated dystonia 
    ... other parts of the body and the movements may become persistent and present when at rest and ... little is known about its function, this protein may help process and transport other proteins within cells. ...
    https://medlineplus.gov/.../condition/early-onset-isolated-dystonia - Genetics
  8. Progressive myoclonic epilepsy type 1 
    ... frequency and severity over time. Episodes of myoclonus may be brought on by physical exertion, stress, light, ... Within 5 to 10 years, the myoclonic episodes may become severe enough to interfere with walking and ...
    https://medlineplus.gov/.../progressive-myoclonic-epilepsy-type-1 - Genetics
  9. McCune-Albright syndrome 
    ... fibrous dysplasia. Polyostotic means the abnormal areas (lesions) may occur in many bones; often they are confined ... the body. Replacement of bone with fibrous tissue may lead to fractures, uneven growth, and deformity. When ...
    https://medlineplus.gov/genetics/condition/mccune-albright-syndrome - Genetics
  10. Tyrosine hydroxylase deficiency 
    ... dystonia), symptoms usually appear during childhood. Affected individuals may have difficulties walking and running, which can sometimes lead to falls. Some people with the disorder may walk on their toes because of stiffness in ...
    https://medlineplus.gov/.../tyrosine-hydroxylase-deficiency - Genetics
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