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Results 11 - 20 of 102 for Eyelid disorder
  1. Horner syndrome 
    ... in about 5 percent of affected individuals, the disorder is present from birth (congenital).Horner syndrome is characterized by drooping of the upper eyelid (ptosis) on the affected side, a constricted pupil ...
    https://medlineplus.gov/genetics/condition/horner-syndrome - Genetics
  2. Dystonia 6 
    ... of dystonia 6 vary among affected individuals. The disorder usually first impacts muscles of the head and neck, causing problems with speaking (dysarthria) and eating (dysphagia). Eyelid twitching (blepharospasm) may also occur. Involvement of one ...
    https://medlineplus.gov/genetics/condition/dystonia-6 - Genetics
  3. Moebius syndrome 
    ... follow the movement of objects. People with this disorder have difficulty making eye contact, and their eyes may not look in the same direction (strabismus). Additionally, the eyelids may not close completely when blinking or sleeping, ...
    https://medlineplus.gov/genetics/condition/moebius-syndrome - Genetics
  4. SETBP1 haploinsufficiency disorder 
    ... inner corner of the eyes (epicanthal folds), droopy eyelids (ptosis), puffiness of the skin around ... of SETBP1 haploinsufficiency disorder is unknown, although it is thought to be ...
    https://medlineplus.gov/.../setbp1-haploinsufficiency-disorder - Genetics
  5. Meesmann corneal dystrophy 
    ... increased sensitivity to light (photophobia), twitching of the eyelids (blepharospasm), ... corneal dystrophy is a rare disorder whose prevalence is unknown. It was first described ...
    https://medlineplus.gov/.../condition/meesmann-corneal-dystrophy - Genetics
  6. Blepharophimosis, ptosis, and epicanthus inversus syndrome 
    ... as various activities in the ovaries, resulting in eyelid malformation and abnormally accelerated maturation of ... the altered gene in each cell is sufficient to cause the disorder.In some cases, an affected person inherits the ...
    https://medlineplus.gov/...s-ptosis-and-epicanthus-inversus-syndrome - Genetics
  7. Hereditary neuralgic amyotrophy 
    ... together (ocular hypotelorism), a narrow opening of the eyelids (short palpebral fissures) with a skin ... is unknown. Variants (also ...
    https://medlineplus.gov/.../hereditary-neuralgic-amyotrophy - Genetics
  8. Jacobsen syndrome 
    ... set ears, widely set eyes (hypertelorism) with droopy eyelids (ptosis), ... bleeding disorder called Paris-Trousseau syndrome. This condition causes a ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  9. Lipoid proteinosis 
    ... Lipid proteinosis Lipoid proteinosis National Organization for Rare Disorders (NORD) LIPOID PROTEINOSIS OF URBACH AND WIETHE PubMed Callizo M, Ibanez-Flores N, Laue J, Cuadrado V, Graell X, Sancho JM. Eyelid lesions in lipoid proteinosis or Urbach-Wiethe disease: ...
    https://medlineplus.gov/genetics/condition/lipoid-proteinosis - Genetics
  10. 3p deletion syndrome 
    ... small head (microcephaly), a small jaw (micrognathia), droopy eyelids (ptosis), malformed ... syndrome is likely a rare disorder; at least 30 cases have been described in ...
    https://medlineplus.gov/genetics/condition/3p-deletion-syndrome - Genetics
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