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diagnosis peds treatment 21hydroxylasedeficiency 21ohd acromegaly adrenal cah classification comparison congenitaladrenalhyperplasia conjugated ddxof depressed dermatology effusion elderly emesis erythroderma genetics
Causes of anemia in infants & children #Diagnosis #Peds #Pediatrics #Differential #Anemia #Causes #Algorithm
Causes of anemia ... Diagnosis #Peds #Pediatrics ... #Differential # ... Anemia #Causes # ... Algorithm
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Causes of Depressed / Lethargic Newborn - Differential Diagnosis Algorithm Maternal Related: • Drugs (Ex. SSRI) •
Causes of Depressed ... Diagnosis Algorithm ... Sepsis Other: • Anemia ... #Causes #Peds # ... Pediatrics
Pediatric Vomiting - Gastrointestinal and Systemic Causes - Differential Diagnosis Algorithm Hepatobiliary: • Acute Hepatitis • Acute
Pediatric Vomiting ... - Differential ... Diagnosis Algorithm ... #Causes #Peds # ... Pediatrics
Erythroderma - Diagnostic Algorithm. Pathophysiology: 1) Extensive cutaneous capillary dilation, results in widespread exfoliation of the
Erythroderma - Diagnostic Algorithm ... Pathophysiology: ... Causes: 1) Exfoliative ... Histamine 4) Skin-homing ... #Differential #
Hyperuricemia - Differential Diagnosis Algorithm Primary - Over-production • Increased turnover of nucleotides Primary
Hyperuricemia - Differential ... Diagnosis Algorithm ... - Hemolytic Anemia ... #endocrinology ... #causes
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Short Stature - Differential ... Diagnosis Algorithm ... #Diagnosis #Algorithm ... #endocrinology ... #causes #pediatrics
Causes of Pleural Effusion - Differential Diagnosis Algorithm Transudate - Hydrostatic • Congestive heart failure • Constrictive
Causes of Pleural ... Effusion - Differential ... Diagnosis Algorithm ... syndrome • Protein-losing ... • Asbestos • Uremia
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Classification of Jaundice Unconjugated hyperbilirubinemia (predominantly indirect bilirubin) • Increased bilirubin production (eg, hemolytic anemias, hemolytic reactions,
(eg, hemolytic anemias ... or mutation in genes ... coding for bile ... #unconjugated #differential ... #causes
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