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Results 1 - 10 of 15 for eyelid disorders
  1. STAC3 gene 
    ... Native American myopathy). This condition is a muscle disorder characterized by weakness, droopy eyelids (ptosis) and other distinctive facial features, joint deformities ( ...
    https://medlineplus.gov/genetics/gene/stac3 - Genetics
  2. CTNND1 gene 
    ... the head and face (craniofacial development), including the eyelids and teeth. At least three CTNND1 gene mutations have been identified in people with blepharocheilodontic (BCD) syndrome, a disorder that is present at birth and causes abnormalities ...
    https://medlineplus.gov/genetics/gene/ctnnd1 - Genetics
  3. CDH1 gene 
    ... identified in people with blepharocheilodontic (BCD) syndrome. This disorder is present at birth and causes abnormalities mainly affecting the eyelids and mouth, including openings on both sides of ...
    https://medlineplus.gov/genetics/gene/cdh1 - Genetics
  4. POLG gene 
    ... condition called progressive external ophthalmoplegia, another POLG-related disorder. This condition weakens the muscles that control eye movement and causes the eyelids to droop (ptosis).There are at least 67 ...
    https://medlineplus.gov/genetics/gene/polg - Genetics
  5. SLC25A4 gene 
    ... an eye condition called progressive external ophthalmoplegia. This disorder weakens the muscles that control eye movement and causes the eyelids to droop (ptosis). When caused by SLC25A4 gene ...
    https://medlineplus.gov/genetics/gene/slc25a4 - Genetics
  6. RRM2B gene 
    ... an eye condition called progressive external ophthalmoplegia. This disorder weakens the muscles that control eye movement and causes the eyelids to droop (ptosis). Some affected individuals have additional ...
    https://medlineplus.gov/genetics/gene/rrm2b - Genetics
  7. MT-TL1 gene 
    ... an eye condition called progressive external ophthalmoplegia. This disorder weakens the muscles that control eye movement and causes drooping eyelids (ptosis).Some cases of progressive external ophthalmoplegia result ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  8. TWNK gene 
    ... an eye condition called progressive external ophthalmoplegia. This disorder weakens the muscles that control eye movement and causes the eyelids to droop (ptosis). Researchers speculate that the mutated ...
    https://medlineplus.gov/genetics/gene/twnk - Genetics
  9. TWIST1 gene 
    ... have been found to cause a very rare disorder called Sweeney-Cox syndrome. This condition is characterized by widely spaced eyes (hypertelorism), abnormal eyelids and ears, unusually small bones in the face ...
    https://medlineplus.gov/genetics/gene/twist1 - Genetics
  10. PLG gene 
    ... identified in people with congenital plasminogen deficiency. This disorder is characterized by hard growths on the mucous membranes, which are the moist tissues that line body openings such as the eyelids and the inside of the mouth. Congenital plasminogen ...
    https://medlineplus.gov/genetics/gene/plg - Genetics
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