| SBT | serum bactericidal titer; single-breath test; sulbactam |
|---|---|
| SC | conditioned stimulus; sacrococcygeal; Sanitary Corps; scalenus [muscle]; scapula; Schwann cell; scia... |
| SCABG | single coronary artery bypass |
| SCBE | single contrast barium enema |
| SCCA | single-cell cytotoxicity assay |
| cystic adenomatoid malformation of lung, congenital | A developmental anomaly that usually becomes apparent in the neonatal period with progressive respiratory distress. This malformation is a focal pulmonary dysplasia characterised by a multicystic mass of terminal bronchiolar structures. Ccam is classified into 3 separate types (I, II, III) depending on cyst size. (12 Dec 1998) |
|---|---|
| heart defects, congenital | Imperfections or malformations of the heart, existing at birth. (12 Dec 1998) |
| hip dislocation, congenital | Congenital dislocation of the hip generally includes subluxation of the femoral head, acetabular dysplasia, and complete dislocation of the femoral head from the true acetabulum. This condition occurs in approximately 1 in 1000 live births and is more common in females than in males. (12 Dec 1998) |
| hyperostosis, cortical, congenital | A disease of young infants characterised by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (12 Dec 1998) |
| nonbullous congenital ichthyosiform erythroderma | Erythroderma or a collodion membrane at birth, usually without improvement during childhood, characterised by proliferation of epidermal keratinocytes with lipid accumulation; autosomal recessive inheritance. (05 Mar 2000) |
| syphilis, congenital | Syphilis acquired in utero and manifested by any of several characteristic tooth (hutchinson's teeth) or bone malformations and by active mucocutaneous syphilis at birth or shortly thereafter. Ocular and neurologic changes may also occur. (12 Dec 1998) |
| disease, congenital heart | A birth defect of the heart or great blood vessels (like the aorta). (12 Dec 1998) |
| double congenital athetosis | A type of cerebral palsy manifested predominantly as bilateral involuntary movements, beginning at about the age of 3 years, and preceded by generalised hypotonia and delayed motor development. Due to various causes, including kernicterus and birth hypoxia. Synonym: congenital choreoathetosis, double congenital athetosis, Vogt syndrome. (05 Mar 2000) |
| ichthyosiform erythroderma, congenital | Designation for several severe forms of ichthyosis, present at birth, that are characterised by hyperkeratotic scaling. Infants may be born encased in a collodion membrane which begins shedding within 24 hours. This is followed in about two weeks by persistent generalised scaling. The forms include bullous (hyperkeratosis, epidermolytic), non-bullous (ichthyosis, lamellar), wet type, and dry type. (12 Dec 1998) |
| toxoplasmosis, congenital | Congenital infection with toxoplasma gondii characterised by lesions of the central nervous system. (12 Dec 1998) |
| foot deformities, congenital | Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth. (12 Dec 1998) |
| limb deformities, congenital | Congenital structural deformities of the upper and lower extremities collectively or unspecified. (12 Dec 1998) |
| acute renal failure | <nephrology> A sudden decline in renal function may be triggered by a number of acute disease processes. Examples include sepsis (infection), shock, trauma, kidney stones, kidney infection, drug toxicity (aspirin or lithium), poisons or toxins (drug abuse) or after injection with an iodinated contrast dye (adverse effect). Chronic renal failure represents a slow decline in kidney function over time. Chronic renal failure may be caused by a number of disorders which include long-standing hypertension, diabetes, congestive heart failure, lupus or sickle cell anaemia. Both forms of renal failure result in a life-threatening metabolic derangement. (27 Sep 1997) |
| aminoaciduria, renal | Impairment of renal tubular transport of amino acids. (12 Dec 1998) |
| back-pressure renal atrophy | <radiology> Caliectasis without obstruction, due to repeated episodes of obstruction, gradual loss of renal pyramids (12 Dec 1998) |