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  2. Muscle–eye–brain disease - Wikipedia

    en.wikipedia.org/wiki/Muscle–eye–brain_disease

    Muscle–eye–brain (MEB) disease, also known as muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A3 (MDDGA3), [2] is a kind of rare congenital muscular dystrophy (CMD), largely characterized by hypotonia at birth. Patients have muscular dystrophy, central nervous system abnormalities and ocular abnormalities.

  3. Duchenne muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Duchenne_muscular_dystrophy

    Another source reports Duchenne muscular dystrophy being a rare disease and having an occurrence of 7.1 per 100,000 male births. [8] A number of sources referenced in this article indicate an occurrence of 6 per 100,000. [9] Duchenne muscular dystrophy is the most common type of muscular dystrophy, [3] with a median life expectancy of 28–30 ...

  4. Stickler syndrome - Wikipedia

    en.wikipedia.org/wiki/Stickler_syndrome

    Many people with Stickler syndrome are very nearsighted (described as having high myopia) because of the shape of the eye. People with eye involvement are prone to increased pressure within the eye (ocular hypertension) which could lead to glaucoma and tearing or detachment of the light-sensitive retina of the eye (retinal detachment).

  5. Granular corneal dystrophy - Wikipedia

    en.wikipedia.org/wiki/Granular_corneal_dystrophy

    Granular corneal dystrophy is caused by a mutation in the TGFBI gene, located on chromosome 5q31. [4] The disorder is inherited in an autosomal dominant manner. [5] This indicates that the defective gene responsible for the disorder is located on an autosome (chromosome 5 is an autosome), and only one copy of the gene is sufficient to cause the disorder, when inherited from a parent who has ...

  6. Eye disease - Wikipedia

    en.wikipedia.org/wiki/Eye_disease

    (H18.5) Fuchs' dystrophy — cloudy morning vision (H18.6) Keratoconus — degenerative disease: the cornea thins and changes shape to be more like a cone than a parabole (H19.3) Keratoconjunctivitis sicca — dry eyes (H20.0) Iritis — inflammation of the iris

  7. Posterior polymorphous corneal dystrophy - Wikipedia

    en.wikipedia.org/wiki/Posterior_polymorphous...

    Posterior polymorphous corneal dystrophy (PPCD; sometimes also Schlichting dystrophy) is a type of corneal dystrophy, characterised by changes in Descemet's membrane and endothelial layer. Symptoms mainly consist of decreased vision due to corneal edema. In some cases they are present from birth, other patients are asymptomatic.

  8. Complex regional pain syndrome - Wikipedia

    en.wikipedia.org/wiki/Complex_regional_pain_syndrome

    Complex regional pain syndrome (CRPS Type 1 and Type 2) is a severe form of chronic pain, in which pain from a physical trauma outlasts the expected recovery time.The symptoms of types 1 and 2 are the same except type 2 is associated with nerve injury.

  9. Corneal endothelium - Wikipedia

    en.wikipedia.org/wiki/Corneal_endothelium

    The corneal endothelium is a single layer of endothelial cells on the inner surface of the cornea.It faces the chamber formed between the cornea and the iris. The corneal endothelium are specialized, flattened, mitochondria-rich cells that line the posterior surface of the cornea and face the anterior chamber of the eye.

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