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  2. Normal pressure hydrocephalus - Wikipedia

    en.wikipedia.org/wiki/Normal_pressure_hydrocephalus

    The disease presents in a classic triad of symptoms, which are memory impairment, urinary frequency, and balance problems/gait deviations (note: this diagnosis method is obsolete [5] [6]). The disease was first described by Salomón Hakim and Raymond Adams in 1965.

  3. Nephronophthisis - Wikipedia

    en.wikipedia.org/wiki/Nephronophthisis

    Nephronophthisis is a genetic disorder of the kidneys which affects children. [3] It is classified as a medullary cystic kidney disease.The disorder is inherited in an autosomal recessive fashion and, although rare, is the most common genetic cause of childhood kidney failure.

  4. Hydrocephalus - Wikipedia

    en.wikipedia.org/wiki/Hydrocephalus

    Hydrocephalus can be classified via mechanism into communicating, noncommunicating, ex vacuo, and normal pressure hydrocephalus. Diagnosis is made by physical examination and medical imaging, such as a CT scan. [1] Hydrocephalus is typically treated through surgery. One option is the placement of a shunt system. [1]

  5. HNRNPH2-related disorders - Wikipedia

    en.wikipedia.org/wiki/HNRNPH2-related_disorders

    A positive diagnosis for HNRNPH2-related disorder is confirmed through reviews of whole exome sequencing genetic reports by qualified medical professionals along with additional information provided by the primary caregivers. Currently there are no cures for HNRNPH2-related disorder, though not all patients require treatment or additional ...

  6. Pantothenate kinase-associated neurodegeneration - Wikipedia

    en.wikipedia.org/wiki/Pantothenate_kinase...

    The disease was renamed 'pantothenate kinase-associated neurodegeneration' or PKAN by Zhou et al. (2001) [3] who suggested the name to avoid misinterpretation and to better reflect the true nature of the disorder. Most recently Pellecchia et al. (2005) published a report of 16 patients affected by PKAN, confirmed by genetic analysis.

  7. L1 syndrome - Wikipedia

    en.wikipedia.org/wiki/L1_syndrome

    L1 syndrome is a group of mild to severe X-linked recessive disorders that share a common genetic basis. The spectrum of L1 syndrome disorders includes X-linked complicated corpus callosum dysgenesis, spastic paraplegia 1, MASA syndrome, and X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS).

  8. Idiopathic intracranial hypertension - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_intracranial...

    The disease was renamed benign intracranial hypertension in 1955 to distinguish it from intracranial hypertension due to life-threatening diseases (such as cancer); [30] however, this was also felt to be misleading because any disease that can blind someone should not be thought of as benign, and the name was therefore revised in 1989 to ...

  9. List of countries by life expectancy - Wikipedia

    en.wikipedia.org/wiki/List_of_countries_by_life...

    UN: Estimate of life expectancy for various ages in 2023; Locations Life expectancy for population in general Life expectancy for male Life expectancy for female Sex gap; at birth bonus 0→15 at 15 bonus 15→65 at 65 bonus 65→80 at 80 at birth at 15 at 65 at 80 at birth at 15 at 65 at 80 at birth at 15 at 65 at 80 Hong Kong: 85.51: 0.21: 70 ...