scad


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ACADS

A gene on chromosome 12q24.31 that encodes a tetrameric mitochondrial flavoprotein of the acyl-CoA dehydrogenase family which catalyses the first step of the mitochondrial fatty acid beta-oxidation pathway.
 
Molecular pathology
Defects in ACADS cause acyl-CoA dehydrogenase short-chain deficiency.

scad

transitory lameness in sheep, reputed to follow frosty conditions and to be a dermatitis caused by cold injury.
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1 years in SCAD group, only one fibromuscular dysplasia (FMD) case concomitant with SCAD was confirmed in the study due to peripheral artery angiography.
12) The Mayo Clinic group reported a 17% recurrence rate of SCAD over a 10-year period.
This finding is the basis for the inflammatory hypothesis about the origin of SCAD [2, 6].
Thrombolytic therapy is relatively contraindicated as its use in some patients with SCAD presenting as ST elevation acute myocardial infarction has led to rapid clinical deterioration after an initial improvement.
Effective management of SCAD therefore relies on early detection and risk stratification of these patients.
Despite the fact that most patients with EMA aciduria have not had their SCAD activity determined, an association between elevated EMA and SCAD has been documented by the presence of either or both of two SCAD gene susceptibility variations in 69% of patients with EMA aciduria (17).
Lennar received a total of 15 video entries from SCAD film students.
The data, demonstrate that RSR was significantly lower in patients with sCAD compared to those with non-significant CAD, and yielded a sensitivity of 83pct and specificity of 70pct.
Dado que la deficiencia primaria o secundaria de SCAD resulta en acumulacion intracelular de butiril-CoA, el cual puede ser convertido en EMA mediante la accion de la propionilCoA carboxilasa y posterior hidrolisis del etilmalonil-CoA (6), el analisis de EMA por cromatografia de gases-espectrometria de masas ha sido considerado un marcador bioquimico de la deficiencia funcional primaria o secundaria de SCAD (7), sin embargo, este hallazgo es comun ademas en pacientes con signos predominantemente neuromusculares y deficiencias en la cadena respiratoria mitocondrial (8), en pacientes con sindrome de encefalopatia etilmalonica (9), y en la enfermedad de los vomitos de Jamaica (10).
An original aim in founding SCAD was to create the best college design program in the world.
To the best of our knowledge this is the first case of SCAD reported in a wrestler.