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  2. Suprarenal plexus - Wikipedia

    en.wikipedia.org/wiki/Suprarenal_plexus

    The suprarenal plexus is formed by branches from the celiac plexus, from the celiac ganglion, and from the phrenic and greater splanchnic nerves, a ganglion being formed at the point of junction with the latter nerve.

  3. Waterhouse–Friderichsen syndrome - Wikipedia

    en.wikipedia.org/wiki/Waterhouse–Friderichsen...

    Waterhouse–Friderichsen syndrome (WFS) is defined as adrenal gland failure due to hemorrhages in the adrenal glands, commonly caused by sepsis. Typically, the bacteria responsible for triggering the bleeding is Neisseria meningitidis .

  4. Albright's hereditary osteodystrophy - Wikipedia

    en.wikipedia.org/wiki/Albright's_hereditary...

    Symptoms: Choroid plexus calcification, Full cheeks [1] Causes: Gs alpha subunit deficiency [2] Diagnostic method: calcium, phosphorus, PTH, Urine test for phosphorus and cyclic AMP: Treatment: Phosphate binders, supplementary calcium [3] Named after: Fuller Albright

  5. Adrenal medulla - Wikipedia

    en.wikipedia.org/wiki/Adrenal_medulla

    The adrenal medulla (Latin: medulla glandulae suprarenalis) is the inner part of the adrenal gland. [1] It is located at the center of the gland, being surrounded by the adrenal cortex. [1]

  6. Celiac plexus - Wikipedia

    en.wikipedia.org/wiki/Celiac_plexus

    The plexus is formed in part by the greater and lesser splanchnic nerves of both sides, and fibers from the anterior and posterior vagal trunks. The celiac plexus proper consists of the celiac ganglia with a network of interconnecting fibers. The aorticorenal ganglia are often considered to be part of the celiac ganglia, and thus, part of the ...

  7. Kearns–Sayre syndrome - Wikipedia

    en.wikipedia.org/wiki/Kearns–Sayre_syndrome

    Treatment with folinic acid can in some cases alleviate the associated symptoms and partially correct associated brain abnormalities, especially if started early in the course of illness. [6] The proposed cause of cerebral folate deficiency in the Kearns–Sayre syndrome is the failure of the mechanisms in the choroid plexus that are ...

  8. Snijders Blok–Campeau syndrome - Wikipedia

    en.wikipedia.org/wiki/Snijders_Blok–Campeau...

    Snijders Blok–Campeau syndrome is a genetic disorder caused by mutations in the CHD3 gene. [1] It is characterized by impaired intellectual development , macrocephaly , dysarthria and apraxia of speech , and certain distinctive facial features .

  9. Landau–Kleffner syndrome - Wikipedia

    en.wikipedia.org/wiki/Landau–Kleffner_syndrome

    Landau–Kleffner syndrome (LKS), also called infantile acquired aphasia, acquired epileptic aphasia, [1] or aphasia with convulsive disorder, is a rare neurological syndrome that develops during childhood. [2] It is named after William Landau and Frank Kleffner, who characterized it in 1957 with a diagnosis of six children. [3] [4]