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diagnosis management treatment 21hydroxylasedeficiency acromegaly cdi cdiff clostridioides clostridium diabetes diabeticketoacidosis difficile dka gastroenterology genetics glftap idsa infection infectiousdiseases macroadenoma
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
approximately 1 ... Signs / Symptoms / Complications ... #SideEffects #endocrinology ... mnemonic #GLFTAP #pathophysiology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
Treating DKA: 1) ... Signs/Symptoms/Complications ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
Usually presents ~5th ... malignancy Pathophysiology ... • Serum IGF-1 ... Diagnosis #Management #Endocrinology ... #Treatment #Pathophysiology
C.diff - Clostridioides Difficile Infection (CDI) - Diagnosis and Management - GrepMed Handbook Clinical Presentation + Progression:
of hospitalized pts ... Perforation) Pathophysiology ... Epidemiology: • #1 ... CT A/P: Assess complications ... 10 mg/kg IV x 1
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