11 results
diagnosis differential neurology hepatology pulmonary 21hydroxylasedeficiency 21ohd algorithm alkaline alp amyotrophic anorexianervosa complications disorders elevation endocrinology evaluation falls fever genetics
Pulmonary Function Tests (PFTs) - Interpretation Algorithm • Normal • Pulmonary Hypertension, Anemia, Carboxyhemoglobinemia • Chest
Pulmonary Function ... Tests (PFTs) - ... Non-Emphysematous COPD ... Emphysematous COPD ... #Pulmonary #FunctionTests
Liver Function Test (LFTs) Elevation AST - Cardiac and skeletal muscle, kidney, brain ALT - More specific for
Liver Function Test ... (LFTs) Elevation ... / ULN ALT) / (ALP ... SinaiBmoreIMRes #Liver #FunctionTest ... #LFTs #Elevation
Causes of Thrombocytopenia and Platelet Disorders - Differential Diagnosis and Workup History: - Prior platelet count, family
Causes of Thrombocytopenia ... smear, HIV/HCV testing ... country), thyroid function ... gastric bypass), LFT ... not required in all
Causes of Neuromuscular Weakness • Spinal Cord: Demyelinating Disease (MS), Epidural abscess, Infarction, Syringomyelia, Tetanus, Transverse
Causes of Neuromuscular ... Weakness • Spinal Cord ... Motor Nerves: ALS ... Neuromuscular junction ... poisoning, Scorpion sting
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
lateral sclerosis Pathophysiology ... disrupt cellular function ... multiple spinal cord ... - Causes progressive ... - Further testing
Hypophosphatemia and Hypoxia - Pathophysiology ↓ Phosphate leads to ↓ red cell 2,3-DPG and a reduction
and Hypoxia - Pathophysiology ... impacts respiratory function ... is a cause of refractory ... phosphorus is seen in COPD ... patients with COPD
Low Alkaline Phosphatase - Hypophosphatasia Is Low Alkaline Phosphatase Of Clinical Importance? ALP enzyme- Discovered in 1923 Low
Most cases diagnosed ... nephrocalcinosis • CPPD ... severe mobility/functional ... collection with EDTA Pathophysiology ... Phosphatase: • Other causes
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... glands • Salt wasting ... infants with "salt wasting ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD #pathophysiology
Evaluation of Recurrent Falls Core Concept: Maintaining an upright posture requires the integrated function of multiple systems. Disruption in
the integrated function ... ) - Spinal cord ... neuron disease (ALS ... weakness, muscle wasting ... fear of falling, functional
Anorexia Nervosa: Complications CARDIAC ABNORMALITIES - Functional: Low BP, Sinus bradycardia, prolonged QT interval - Structural: Reduced
ABNORMALITIES - Functional ... Enzymes - From fasting ... Hypothermia and Cold ... mortality rates of all ... Complications #pathophysiology
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