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    40.14+1.49 (+3.86%)

    at Fri, May 31, 2024, 4:00PM EDT - U.S. markets closed

    Nasdaq Real Time Price

    • Open 39.48
    • High 40.74
    • Low 39.14
    • Prev. Close 38.65
    • 52 Wk. High 54.98
    • 52 Wk. Low 31.52
    • P/E N/A
    • Mkt. Cap 3.34B
  1. Results From The WOW.Com Content Network
  2. Intersex - Wikipedia

    en.wikipedia.org/wiki/Intersex

    Intersex people are individuals born with any of several underlying genetic conditions that cause abnormal development of sex characteristics including chromosome patterns, gonads, or genitals that, according to the Office of the United Nations High Commissioner for Human Rights, "do not fit typical binary notions of male or female bodies".

  3. Treacher Collins syndrome - Wikipedia

    en.wikipedia.org/wiki/Treacher_Collins_syndrome

    Treacher Collins syndrome ( TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. [5] The degree to which a person is affected, however, may vary from mild to severe. [5] Complications may include breathing problems, problems seeing, cleft palate, and hearing loss. [5]

  4. Polymelia - Wikipedia

    en.wikipedia.org/wiki/Polymelia

    Polymelia is a birth defect in which an affected individual has more than the usual number of limbs. It is a type of dysmelia. In humans and most land-dwelling vertebrates, this means having five or more limbs. The extra limb is most commonly shrunken and/or deformed. The term is from Greek πολυ- "many", μέλεα "limbs".

  5. Genetic disorder - Wikipedia

    en.wikipedia.org/wiki/Genetic_disorder

    Most genetic disorders are rare in themselves. [5] [8] Genetic disorders are present before birth, and some genetic disorders produce birth defects, but birth defects can also be developmental rather than hereditary. The opposite of a hereditary disease is an acquired disease.

  6. Baby with extremely rare defect born with one eye in ... - AOL

    www.aol.com/article/2015/10/06/baby-with...

    The baby suffers from cyclopia, one of the rarest birth defects that often causes children to die within moments of birth. The baby only has one eye because his eye sockets did not form correctly ...

  7. Harlequin-type ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Harlequin-type_ichthyosis

    Death in the first month is relatively common [6] Frequency. 1 in 300,000 [7] Harlequin-type ichthyosis is a genetic disorder that results in thickened skin over nearly the entire body at birth. [4] The skin forms large, diamond/trapezoid/rectangle-shaped plates that are separated by deep cracks. [4] These affect the shape of the eyelids, nose ...

  8. Genetic diagnosis of intersex - Wikipedia

    en.wikipedia.org/wiki/Genetic_diagnosis_of_intersex

    Intersex people's right to life can be violated in discriminatory "sex selection" and "preimplantation genetic diagnosis, other forms of testing, and selection for particular characteristics". Such de-selection or selective abortions are incompatible with ethics and human rights standards due to the discrimination perpetrated against intersex ...

  9. Polydactyly - Wikipedia

    en.wikipedia.org/wiki/Polydactyly

    Polydactyly or polydactylism (from Greek πολύς (polys) 'many', and δάκτυλος (daktylos) 'finger'), also known as hyperdactyly, is an anomaly in humans and non-human animals resulting in supernumerary fingers and/or toes. Polydactyly is the opposite of oligodactyly (fewer fingers or toes).

  10. Proteus syndrome - Wikipedia

    en.wikipedia.org/wiki/Proteus_syndrome

    Proteus syndrome is a rare disorder with a genetic background [1] that can cause tissue overgrowth involving all three embryonic lineages. Patients with Proteus syndrome tend to have an increased risk of embryonic tumor development. [2]

  11. Cyclopia - Wikipedia

    en.wikipedia.org/wiki/Cyclopia

    Cyclopia (named after the Greek mythology character cyclopes ), also known as alobar holoprosencephaly, is the most extreme form of holoprosencephaly and is a congenital disorder (birth defect) characterized by the failure of the embryonic prosencephalon to properly divide the orbits of the eye into two cavities.