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  2. Esotropia - Wikipedia

    en.wikipedia.org/wiki/Esotropia

    Where appropriate, prismatic correction can be used, either temporarily or permanently, to relieve symptoms of double vision. In specific cases, and primarily in adult patients, botulinum toxin can be used either as a permanent therapeutic approach, or as a temporary measure to prevent contracture of muscles prior to surgery

  3. Convergence insufficiency - Wikipedia

    en.wikipedia.org/wiki/Convergence_insufficiency

    Symptoms. The symptoms and signs associated with convergence insufficiency are related to prolonged, visually demanding, near-centered tasks. They may include, but are not limited to, diplopia (double vision), asthenopia (eye strain), transient blurred vision, difficulty sustaining near-visual function, abnormal fatigue, headache, and abnormal ...

  4. Darier's disease - Wikipedia

    en.wikipedia.org/wiki/Darier's_disease

    Darier's disease. Darier's disease (DAR) is a rare, inherited skin disorder that presents with multiple greasy, crusting, thick brown bumps that merge into patches. [4] It is an autosomal dominant disorder discovered by French dermatologist Ferdinand-Jean Darier . Mild forms of the disease are the most common, consisting solely of skin rashes ...

  5. Esophoria - Wikipedia

    en.wikipedia.org/wiki/Esophoria

    Esophoria is an eye condition involving inward deviation of the eye, usually due to extra-ocular muscle imbalance. It is a type of heterophoria. Cause. Causes include: Refractive errors; Divergence insufficiency; Convergence excess; this can be due to nerve, muscle, congenital or mechanical anomalies.

  6. Heterophoria - Wikipedia

    en.wikipedia.org/wiki/Heterophoria

    Heterophoria is the misalignment of the visual axis such that one or both eyes are not properly fixated to an object of interest. When the visual axis is misaligned in such a way, it is corrected by the fusional vergence system. Diagnosis. The cross-cover test, or alternating cover test is usually employed to detect heterophoria.

  7. Parry–Romberg syndrome - Wikipedia

    en.wikipedia.org/wiki/Parry–Romberg_syndrome

    Parry–Romberg syndrome (PRS) is a rare disease presenting in early childhood characterized by progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face (hemifacial atrophy) but occasionally extending to other parts of the body.

  8. Toxic epidermal necrolysis - Wikipedia

    en.wikipedia.org/wiki/Toxic_epidermal_necrolysis

    Characteristic skin loss of toxic epidermal necrolysis: Specialty: Dermatology: Symptoms: Fever, skin blisters, skin peeling, painful skin, red eyes: Complications: Dehydration, sepsis, pneumonia, multiple organ failure. Usual onset: Age > 40: Risk factors: HIV/AIDS, systemic lupus erythematosus, genetics: Diagnostic method

  9. Schamberg disease - Wikipedia

    en.wikipedia.org/wiki/Schamberg_disease

    Schamberg's disease causes no other symptoms beside skin discoloration and itching. The condition is caused by inflammation of capillaries near the surface of skin and subsequent leaking of red blood cells into surrounding tissues.

  10. Haim–Munk syndrome - Wikipedia

    en.wikipedia.org/wiki/Haim–Munk_syndrome

    Symptoms. Most of the signs of Haim–Munk syndrome begin to manifest during the first 2–4 years of life. [5] Commons signs at this stage are thickening and scaling of the skin of the palms, soles ( palmoplantar keratoderma) and elbows, and shedding of the primary dentition caused by recurrent episodes of dental caries and periodontitis.

  11. Keratolytic winter erythema - Wikipedia

    en.wikipedia.org/wiki/Keratolytic_winter_erythema

    Keratolytic Winter erythema (also known as Oudtshoorn disease [1] or Oudtshoorn skin [2] [3]) is a rare autosomal dominant skin disease of unknown cause which causes redness and peeling of the skin on the palms and soles. [4] Onset, increased prominence and severity usually occurs during winter. [5] [6] It is a type of genodermatosis.