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  2. International Classification of Diseases - Wikipedia

    en.wikipedia.org/wiki/International...

    The International Classification of Diseases, Clinical Modification (ICD-9-CM) was an adaptation created by the US National Center for Health Statistics (NCHS) and used in assigning diagnostic and procedure codes associated with inpatient, outpatient, and physician office utilization in the United States. The ICD-9-CM is based on the ICD-9 but ...

  3. Pseudobulbar affect - Wikipedia

    en.wikipedia.org/wiki/Pseudobulbar_affect

    Pseudobulbar affect (PBA), or emotional incontinence, is a type of neurological disorder characterized by uncontrollable episodes of crying or laughing.PBA occurs secondary to a neurologic disorder or brain injury.

  4. Post-concussion syndrome - Wikipedia

    en.wikipedia.org/wiki/Post-concussion_syndrome

    The ICD-10 established a set of diagnostic criteria for PCS in 1992. [38] In order to meet these criteria, a patient has had a head injury "usually sufficiently severe to result in loss of consciousness" [33] [39] and then develop at least three of the eight symptoms marked with a check mark in the table at right under "ICD-10" within four weeks.

  5. Complex regional pain syndrome - Wikipedia

    en.wikipedia.org/wiki/Complex_regional_pain_syndrome

    Diagnosis is primarily based on clinical findings. The original diagnostic criteria for CRPS adopted by the International Association for the Study of Pain (IASP) in 1994 have now been superseded in both clinical practice and research by the "Budapest Criteria" which were created in 2003 and have been found to be more sensitive and specific. [33]

  6. Hashimoto's encephalopathy - Wikipedia

    en.wikipedia.org/wiki/Hashimoto's_encephalopathy

    Hashimoto's encephalopathy, also known as steroid-responsive encephalopathy associated with autoimmune thyroiditis ( SREAT ), is a neurological condition characterized by encephalopathy, thyroid autoimmunity, and good clinical response to corticosteroids. It is associated with Hashimoto's thyroiditis, and was first described in 1966.

  7. Waldenström macroglobulinemia - Wikipedia

    en.wikipedia.org/wiki/Waldenström_macroglobulinemia

    Waldenström macroglobulinemia is characterized by an uncontrolled clonal proliferation of terminally differentiated B lymphocytes. The most commonly associated mutations, based on whole-genome sequencing of 30 patients, are a somatic mutation in MYD88 (90% of patients) and a somatic mutation in CXCR4 (27% of patients). [ 11]

  8. Primary lateral sclerosis - Wikipedia

    en.wikipedia.org/wiki/Primary_lateral_sclerosis

    Primary lateral sclerosis ( PLS) is a very rare neuromuscular disease characterized by progressive muscle weakness in the voluntary muscles. PLS belongs to a group of disorders known as motor neuron diseases. Motor neuron diseases develop when the nerve cells that control voluntary muscle movement degenerate and die, causing weakness in the ...

  9. Polycythemia vera - Wikipedia

    en.wikipedia.org/wiki/Polycythemia_vera

    In oncology, polycythemia vera ( PV) is an uncommon myeloproliferative neoplasm in which the bone marrow makes too many red blood cells. [ 1] The majority of cases [ 2] are caused by mutations in the JAK2 gene, most commonly resulting in a single amino acid change in its protein product from valine to phenylalanine at position 617.