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Results 1 - 10 of 23 for Pupil disorder
  1. Stormorken syndrome 
    ... the muscles that control the size of the pupils. Other features include lack of a functioning spleen (asplenia), scaly skin (ichthyosis), headaches, and difficulty with reading and spelling (dyslexia). Stormorken syndrome is a rare disorder. Approximately a dozen cases have been reported in ...
    https://medlineplus.gov/genetics/condition/stormorken-syndrome - Genetics
  2. Horner syndrome 
    ... in the affected eye (miosis) resulting in unequal pupil size (anisocoria), and absent sweating (anhidrosis) on the affected side of the face. Sinking of the eye into its cavity (enophthalmos) and a bloodshot eye often occur in this disorder. In people with Horner syndrome that occurs before ...
    https://medlineplus.gov/genetics/condition/horner-syndrome - Genetics
  3. Congenital central hypoventilation syndrome 
    ... eye abnormalities, including a decreased response of the pupils to light. ... the severity of the disorder, timing of the diagnosis, and the success of ...
    https://medlineplus.gov/...ngenital-central-hypoventilation-syndrome - Genetics
  4. Aniridia 
    Aniridia is an eye disorder characterized by a complete or partial absence of the colored part of the eye (the iris). These iris abnormalities may cause the pupils to be abnormal or misshapen. Aniridia can cause reduction in the sharpness of vision (visual acuity) and increased sensitivity to ...
    https://medlineplus.gov/genetics/condition/aniridia - Genetics
  5. ACTA2 gene 
    ... gene causes multisystemic smooth muscle dysfunction syndrome. This disorder impairs the activity of smooth muscles throughout the body and leads to widespread problems including blood vessel abnormalities, decreased response of the pupils to light, a weak (hypotonic) bladder, and impairment ...
    https://medlineplus.gov/genetics/gene/acta2 - Genetics
  6. Aromatic l-amino acid decarboxylase deficiency 
    ... can include droopy eyelids (ptosis), constriction of the pupils of the eyes ... AADC deficiency is a rare disorder. Only about 100 people with this condition have ...
    https://medlineplus.gov/...tic-l-amino-acid-decarboxylase-deficiency - Genetics
  7. Norrie disease 
    Norrie disease is an inherited eye ... a sign called leukocoria. The irises (colored portions of the eyes) or the entire ...
    https://medlineplus.gov/genetics/condition/norrie-disease - Genetics
  8. Leber congenital amaurosis 
    ... that detects light and color. People with this disorder typically have ... (hyperopia). The pupils, which usually expand and contract in response to ...
    https://medlineplus.gov/.../condition/leber-congenital-amaurosis - Genetics
  9. Axenfeld-Rieger syndrome 
    Axenfeld-Rieger syndrome is primarily an ... syndrome often have a pupil that is off-center (corectopia) or extra holes ...
    https://medlineplus.gov/genetics/condition/axenfeld-rieger-syndrome - Genetics
  10. Congenital plasminogen deficiency 
    ... line the eyelids. A characteristic feature of this disorder is ligneous ... of the eye (the iris) and pupil. Such growths can tear the cornea or cause ...
    https://medlineplus.gov/.../congenital-plasminogen-deficiency - Genetics
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