Rash Differential peds algorithm pediatrics congenital endocrinology genetics newborn adrenal 21ohd failuretothrive

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

also known as "congenital ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics ... #endocrinology ... #peds #pediatrics

Causes of Failure to Thrive - Differential Diagnosis Algorithm
Adequate Calorie Consumption
- Increased Losses:

Diagnosis Algorithm ... Esophagitis • Congenital ... Relationship #FailuretoThrive ... #Causes #Peds # ... Pediatrics

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