6 results
diagnosis hepatology management neurology 21hydroxylasedeficiency 21ohd abnormal alkaline alp als amyotrophic anorexianervosa complications differential endocrinology genetics hyophosphatasia lateral lfts liver
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... coding for the enzyme ... the amount of enzyme ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD #pathophysiology
Abnormal liver function tests algorithm. This figure details the initial response to abnormal liver blood tests.
Abnormal liver function ... tests algorithm ... decision for repeat testing ... the magnitude of enzyme ... LFTs #Abnormal #Algorithm
Stiff Person Syndrome (SPS) - Diagnosis and Management Summary Epidemiology: • Prevalence: 1-2 cases per million -
Person Syndrome Pathophysiology ... brain and spinal cord ... Clinical Manifestations ... disorders • Testing ... works against an enzyme
Low Alkaline Phosphatase - Hypophosphatasia Is Low Alkaline Phosphatase Of Clinical Importance? ALP enzyme- Discovered in 1923 Low
Phosphatase Of Clinical ... ALP enzyme- Discovered ... nephrocalcinosis • CPPD ... severe mobility/functional ... collection with EDTA Pathophysiology
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
combination of the clinical ... lateral sclerosis Pathophysiology ... disrupt cellular function ... multiple spinal cord ... - Further testing
Anorexia Nervosa: Complications CARDIAC ABNORMALITIES - Functional: Low BP, Sinus bradycardia, prolonged QT interval - Structural: Reduced
ABNORMALITIES - Functional ... Elevated Hepatic Enzymes ... - From fasting/ ... Hypothermia and Cold ... Complications #pathophysiology
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