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21hydroxylasedeficiency endocrinology genetics infant pathophysiology tachypnea wheeze wheezing
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... endocrinology #peds ... #pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider - Bronchiolitis - Pneumonia
tachypnea or wheeze - Clinical ... Other causes #Diagnosis ... #Peds #Pediatrics ... Tachypnea #Wheeze #Differential ... #Assessment #Wheezing
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