enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Albinism in humans - Wikipedia

    en.wikipedia.org/wiki/Albinism_in_humans

    Albinism is a congenital condition characterized in humans by the partial or complete absence of pigment in the skin, hair and eyes. Albinism is associated with a number of vision defects, such as photophobia, nystagmus, and amblyopia. Lack of skin pigmentation makes for more susceptibility to sunburn and skin cancers.

  3. Hermansky–Pudlak syndrome - Wikipedia

    en.wikipedia.org/wiki/Hermansky–Pudlak_syndrome

    HeÅ™manský–Pudlák syndrome (often written Hermansky–Pudlak syndrome or abbreviated HPS) is an extremely rare autosomal recessive [1] disorder which results in oculocutaneous albinism (decreased pigmentation), bleeding problems due to a platelet abnormality (platelet storage pool defect), and storage of an abnormal fat-protein compound (lysosomal accumulation of ceroid lipofuscin).

  4. List of systemic diseases with ocular manifestations - Wikipedia

    en.wikipedia.org/wiki/List_of_systemic_diseases...

    An ocular manifestation of a systemic disease is an eye condition that directly or indirectly results from a disease process in another part of the body. There are many diseases known to cause ocular or visual changes.

  5. Your eyes could signal a major health problem - AOL

    www.aol.com/lifestyle/2017-03-30-eyes-signs...

    Your eyes could signal a major health problem. March 30, 2017 at 2:47 PM. As it turns out, your eyes could be raising some major red flags about your health, according to Dr. Oz The Good Life.

  6. Waardenburg syndrome - Wikipedia

    en.wikipedia.org/wiki/Waardenburg_syndrome

    Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin.

  7. Ocular albinism - Wikipedia

    en.wikipedia.org/wiki/Ocular_albinism

    Ocular albinism, type 1 (OA1) 300500: GPR143: Also known as Nettleship–Falls syndrome, [4] [5] [6] is the most common variety of ocular albinism. OA1 is usually associated with nystagmus, and difficult to otherwise detect in females; males show more readily observable symptoms. Ocular albinism, type 2 (OA2) 300600: CACNA1F [7]

  8. Oculocutaneous albinism - Wikipedia

    en.wikipedia.org/wiki/Oculocutaneous_albinism

    Oculocutaneous albinism is a form of albinism involving the eyes , the skin (-cutaneous), and the hair. [1] Overall, an estimated 1 in 20,000 people worldwide are born with oculocutaneous albinism. [1] OCA is caused by mutations in several genes that control the synthesis of melanin within the melanocytes. [2]

  9. Hallermann–Streiff syndrome - Wikipedia

    en.wikipedia.org/wiki/Hallermann–Streiff_syndrome

    Patients also have eye problems including reduced eye size, bilateral cataracts [2] and glaucoma. The syndrome can be associated with sleep apnea. [3] The physical characteristics of the syndrome can result in difficult intubation by medical professionals. [4] Intelligence is usually normal. [5]