6 results
peds genetics signs 21hydroxylasedeficiency 21ohd cah congenital deficiency diabetes diabeticketoacidosis diagnosis dka hydroxylase hyperplasia immunization praderwilli syndrome upper urinarytractinfection uuti
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
Deficiency - Signs and Symptoms ... Bone: Accelerated childhood ... density, Adult short ... Deficiency #Signs #Symptoms ... #diagnosis #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... /Complications: ... fractures • Short ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Upper Urinary Tract infection (UUTI): Pathogenesis and Clinical Findings Predisposing Factors: - Immunocompromised, Diabetes, - Elderly, Female
Elderly, Female (short ... lower tract: As a complication ... them to adhere to renal ... UrinaryTractInfection #UUTI #Pathophysiology ... #Signs #Symptoms
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
Childhood Immunization ... Tetanus Toxin -> Spores ... lymph -> Koplik's spots ... Immunization #peds #pediatrics ... #pathophysiology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
patient has good renal ... Signs/Symptoms/Complications ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
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