Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 11 - 20 of 35 for Abnormal eyelid movement
  1. Aromatic l-amino acid decarboxylase deficiency 
    ... neurotransmitters contribute to the developmental delays, intellectual disabilities, abnormal movements, and autonomic nervous system dysfunction seen in people ...
    https://medlineplus.gov/...tic-l-amino-acid-decarboxylase-deficiency - Genetics
  2. Myasthenia gravis 
    ... muscles around the eyes, causing drooping of the eyelids (ptosis) and difficulty coordinating eye movements, which results in blurred or double vision. In ...
    https://medlineplus.gov/genetics/condition/myasthenia-gravis - Genetics
  3. Kearns-Sayre syndrome 
    ... paralysis of the eye muscles that impairs eye movement and causes drooping eyelids (ptosis). Affected individuals also have an eye condition ...
    https://medlineplus.gov/genetics/condition/kearns-sayre-syndrome - Genetics
  4. Pearson syndrome 
    ... condition. Some people with Pearson syndrome have droopy eyelids (ptosis), vision problems, hearing loss, seizures, or movement disorders. About half of children with this severe ...
    https://medlineplus.gov/genetics/condition/pearson-syndrome - Genetics
  5. Dihydrolipoamide dehydrogenase deficiency 
    ... deficiency experience weakness of the muscles used for movement (skeletal muscles), particularly during exercise; droopy eyelids; or a weakened heart muscle (cardiomyopathy). Other features ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics
  6. Idiopathic inflammatory myopathy 
    ... by a reddish or purplish rash on the eyelids, elbows, knees, or knuckles. Sometimes, abnormal calcium deposits form hard, painful bumps under the ...
    https://medlineplus.gov/.../idiopathic-inflammatory-myopathy - Genetics
  7. STAC3 disorder 
    ... also be born with joint deformities that restrict movement (contractures) or develop an abnormal side-to-side or back-to-front curvature ...
    https://medlineplus.gov/genetics/condition/stac3-disorder - Genetics
  8. Spinocerebellar ataxia type 36 
    ... lead to involuntary eye movements (nystagmus), rapid eye movements (saccades), trouble moving the eyes side-to-side (oculomotor apraxia), and droopy eyelids (ptosis). Sensorineural hearing loss, which is hearing loss ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  9. Lacrimo-auriculo-dento-digital syndrome 
    ... affected. It can be shorter than normal with abnormal wrist and elbow joint development that limits movement.People with LADD syndrome may also experience other ...
    https://medlineplus.gov/.../lacrimo-auriculo-dento-digital-syndrome - Genetics
  10. Moebius syndrome 
    ... side to side to read or 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
previous · 1 · 2 · 3 · 4 · next