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diagnosis differential peds endocrinology em neurology 21hydroxylasedeficiency 21ohd acute adrenal alzheimersdisease barre blood cah childhood clinical comparison congenitaladrenalhyperplasia constipation cough
Causes of Acute Pediatric Cough - Differential Diagnosis Algorithm No Fever, No Tachypnea - Normal Chest Auscultation
Causes of Acute ... Pediatric Cough ... Bronchitis - No URTI Symptoms ... #Causes #Peds # ... Pediatrics
Causes of Pediatric Stridor - Differential Diagnosis Algorithm Present Since Infancy with No Respiratory Distress: • Laryngomalacia Present
Causes of Pediatric ... Differential Diagnosis Algorithm ... Differential #Diagnosis #Algorithm ... #Causes #Peds # ... Pediatrics #Pulmonary
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... Endocrinology #Adrenal #pathophysiology
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
factor for Late Onset ... chromosome 21) Signs / Symptoms ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Hematuria Workup and Diagnosis Algorithm • Confirm hematuria → Urinalysis >3 RBCs/HPF, exclude mimics, repeat testing
and Diagnosis Algorithm ... testing • Acute onset ... nephrolithiasis • Symptoms ... Nephrology if cause ... identified by UW IM
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
infection -> Sudden onset ... hemorrhagic rash; symptoms ... non-specific viral symptoms ... Immunization #peds #pediatrics ... #pathophysiology
Differential Diagnosis and Evaluation of Hyponatremia: 1) Identification of onset (acute vs. chronic) 2) Presence of symptoms (HA,
Identification of onset ... 2) Presence of symptoms ... (HA, nausea, confusion ... Diagnosis #EM #IM ... #Differential #Algorithm
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... Normal Puberty Onset ... Differential #Diagnosis #Algorithm ... endocrinology #causes ... #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Cullen's sign. Lipase 1,781. Bruising in the skin around the umbilicus. This sign is named after
conditions that cause ... Pathophysiology: ... pregnancy, or other causes ... of other symptoms ... #peritonitis #IM
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