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SCID Severe Combined Immuno-Deficiency; ÁßÁõ º¹ÇÕ ¸é¿ª °áÇÌÁõ
SARS Severe Acute Respiratory Syndrome
BASA Boston Assessment of Severe Aphasia
CIN 2, CIN II cervical intraepithelial neoplasia, grade 2 (moderate-severe)
CIN 3, CIN III cervical intraepithelial neoplasia, grade 3 (severe dysplasia and carcinoma in situ)
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SCID Severe Combined ImmunoDeficient
SCID Severe Combined Immunodeficiency Disease
SMR Severe Mental Retardation
SAP Severe acute pancreatitis
SCARMD Severe childhood autosomal recessive muscular dystrophy
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  • D81.0
    Severe combined immunodeficiency [SCID] with reticular dysgenesis
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  • F32.3
    Severe depressive episode with psychotic symptoms
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  • F32.2
    Severe depressive episode without psychotic symptoms
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  • F53.1
    Severe mental and behavioural disorders associated with the puerperium, NEC
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    Severe mental retardation
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severe acute respiratory distress syndrome ABBR: SARS. A highly contagious, potentially lethal viral respiratory illness first diagnosed in the People's Republic of China in November 2002, characterized by a fever of higher than 100.4¡ÆF, cough,
Ãâó:
severe combined i. a group of rare congenital disorders characterized by gross impairment of both humoral and cell-mediated immunity and absence of T lymphocytes; some forms are also characterized by a lack of B lymphocytes. In most cases all classes of immunoglobulins are nearly or completely absent, and there is marked lymphocytopenia. Persistent diarrhea, chronic mucocutaneous candidiasis, and failure to thrive occur in infancy. Blood transfusions can result in graft-versus-host disease and routine vaccinations in fatal infection. Unless immune function is restored by a histocompatible bone marrow or fetal tissue transplant or the patient is kept in gnotobiotic isolation, death from opportunistic infection usually occurs before the first birthday. In approximately 50 per cent of cases, the disorder is X-linked and due to a defect in the γ chain of the receptor for IL-2 and other interleukins. B lymphocyte numbers are usually normal. The remaining 50 per cent of cases are of autosomal recessive inheritance and have varying etiologies, with approximately half of these due to a defect in either adenosine deaminase or, rarely, purine-nucleoside phosphorylase activity. A rare type of the autosomal recessive form is called reticular dysgenesis.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
severe combined immunodeficiency d. see under immunodeficiency.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
severe congenital n. infantile genetic agranulocytosis.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
severe h. that in which core body temperature is between 9°C (48.2°F) and 28°C (82.4°F).
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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severe extreme plainness
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