851 results
diagnosis symptoms signs differential management pharmacology cardiology endocrinology nephrology syndrome algorithm causes hematology hepatology infectiousdiseases complications msk lifecycle ophthalmology cdc
Purple Urine Bag Syndrome Chronic, indwelling catheter + bacteriuria (Providencia, Klebsiella, E.coli*) + alkaline urine Tryptophan → Indoxyl
sulfate → Sulfatase enzyme ... Syndrome #PUBS #pathophysiology
Steroid Synthesis Pathway (OH, hydroxy; HSD, hydroxysteroid dehydrogenase; DHEA, dehydroepiandrosterone; pink, common enzymes affecting CAH, purple –
; pink, common enzymes ... Pathway #metabolism #pathophysiology
Heme Synthesis Pathway Enzymes 1. ALA Synthase 2. ALA Dehydratase 3. Porphobilinogen deaminase 4. UP Ill Synthase 5. UP Ill Decarboxylase 6. Coproporphyrinogen
Synthesis Pathway Enzymes ... Synthesis #Pathway #pathophysiology
Uric Acid Homeostasis In the liver, purines are metabolized to uric acid. The last step in purine
metabolism involves an enzyme ... In animals, the enzyme ... Homeostasis #Gout #Pathophysiology
Mechanisms of Drug-Induced Hyperkalemia • Direct renin inhibitor (Aliskiren) • Renin release inhibition (NSAIDs, Beta-Blockers)
Angiotensin-converting enzyme ... differential #diagnosis #pathophysiology
Systemic Lupus Erythematosus: Gastrointestinal Manifestations - Thrombosis of vessels in the pancreas, Vasculitis -> Acute Pancreatitis
Elevated Liver Enzymes ... Complications #pathophysiology
Inflammatory Cascade: Pathogenesis and Clinical Findings Continued Innate Immunity • Phagocytosis: (main mechanism) neutrophils and macrophages engulf
puncture holes), enzyme-mediated ... #Inflammation #pathophysiology
Complications of Measles: Pathogenesis and Clinical Findings • ADEM -> Fever, headache, neck stiffness, BBD, mental
elevated liver enzymes ... signs #symptoms #pathophysiology
Renin-Angiotensin-Aldosterone System (RAAS) The kidneys produce renin in response to low blood pressure or low plasma
angiotensin-converting enzyme ... #Pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
coding for the enzyme ... the amount of enzyme ... #21HydroxylaseDeficiency #21OHD #pathophysiology
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