6 results
diagnosis signs 21hydroxylasedeficiency 21ohd addisons anxiety behavioraldisorder diabetes diabeticketoacidosis disease dka hematology hemeonc hemophagocytic henochscholeinpurpura hlh hsp iga insufficiency lymphohistiocytosis
Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
Tuberculosis: can cause ... C deficiency, anticoagulation ... Androgens: • Symptoms ... physical: - Symptoms ... addisons #disease #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... 21-OHD in the adrenal ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
out of cells may cause ... patient has good renal ... Signs/Symptoms/Complications ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
predisposition - Various genetic ... periumbilical region), nausea ... Intussusception - Renal ... HenochScholeinPurpura #Pathophysiology ... Diagnosis #Signs #Symptoms
Panic Disorder: Pathogenesis and clinical findings Social Factors • Parenting and infant attachment • Childhood illness/abuse •
hypothalamic-pituitary-adrenal ... Neurotic personality Genetics ... sweating, trembling, nausea ... BehavioralDisorder #Pathophysiology ... #diagnosis #symptoms
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... or triggers) is crucial ... Familial) HLH: - Genetic ... Common Signs and Symptoms ... Pathophysiology
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