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diagnosis management pediatrics 21hydroxylasedeficiency 21ohd amyotrophic chloride differential disease endocrinology genetics hematology hemeonc hemophagocytic hlh hypochloremia incomplete kawasaki lateral lymphohistiocytosis
Hypochloremia - Differential Diagnosis Algorithm Cause - Decreased Intake: • Low salt in diet • Exclusive D5W
Differential Diagnosis Algorithm ... Cause - Decreased ... - Gitelman SIGNS ... Hypotension • AMS ... #Pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... • This is also ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
lateral sclerosis Pathophysiology ... - Causes progressive ... - Fatigue and decreased ... Escorial criteria uses ... diagnosis column Treatment
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... lack of tapering, decreased ... echo is positive, treatment ... clinical and lab signs ... #Diagnosis #Peds
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... • In all patients ... Onset: Usually in infancy ... Presentation • Common Signs ... Pathophysiology
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