enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Lissencephaly - Wikipedia

    en.wikipedia.org/wiki/Lissencephaly

    Lissencephaly (/ ˌ l ɪ s. ɛ n ˈ s ɛ f. ə l. i /, meaning 'smooth brain') [1] is a set of rare brain disorders whereby the whole or parts of the surface of the brain appear smooth. [2] It is caused by defective neuronal migration during the 12th to 24th weeks of gestation, resulting in a lack of development of brain folds and grooves . [3]

  3. Fursona - Wikipedia

    en.wikipedia.org/wiki/Fursona

    The term "fursona" is a portmanteau of the words "furry" and "persona". [1] The term was first used in 1997. [2]According to Fred Patten, it was common for attendants to use their real names or nicknames at ConFurence (world's first furry convention) in 1989.

  4. Diprosopus - Wikipedia

    en.wikipedia.org/wiki/Diprosopus

    A local doctor told reporters that the baby should be considered a healthy child who currently was living a normal life, a previously unknown occurrence among sufferers of the disorder. [ 21 ] Lali's two middle eyes suffered from corneal opacity due to abnormal anatomy of the facial muscles, which prevented her from properly closing those eyes ...

  5. List of fetal abnormalities - Wikipedia

    en.wikipedia.org/wiki/List_of_fetal_abnormalities

    Fetal abnormalities are conditions that affect a fetus or embryo, are able to be diagnosed prenatally, and may be fatal or cause disease after birth. They may include aneuploidies , structural abnormalities, or neoplasms.

  6. Anencephaly - Wikipedia

    en.wikipedia.org/wiki/Anencephaly

    Anencephaly is the absence of a major portion of the brain, skull, and scalp that occurs during embryonic development. [1] It is a cephalic disorder that results from a neural tube defect that occurs when the rostral (head) end of the neural tube fails to close, usually between the 23rd and 26th day following conception. [2]

  7. Pontocerebellar hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Pontocerebellar_hypoplasia

    Pontocerebellar hypoplasia (PCH) is a heterogeneous group of rare neurodegenerative disorders caused by genetic mutations and characterised by progressive atrophy of various parts of the brain such as the cerebellum or brainstem (particularly the pons). [1]

  8. Primary familial brain calcification - Wikipedia

    en.wikipedia.org/wiki/Primary_familial_brain...

    Primary familial brain calcification [1] (PFBC), also known as familial idiopathic basal ganglia calcification (FIBGC) and Fahr's disease, [1] is a rare, [2] genetically dominant or recessive, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement.

  9. Microcephaly - Wikipedia

    en.wikipedia.org/wiki/Microcephaly

    A mother holding her son who was born with microcephaly due to vertically transmitted infection with Zika virus. Microcephaly (from Neo-Latin microcephalia, from Ancient Greek μικρός mikrós "small" and κεφαλή kephalé "head" [2]) is a medical condition involving a smaller-than-normal head. [3]