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diagnosis 21hydroxylasedeficiency 21ohd breast differential genetics infant pathophysiology pediatrics
Algorithm for the evaluation of the crying infant #Diagnosis #EM #Peds #Crying #Infant #Algorithm
Algorithm for the ... evaluation of the crying ... infant #Diagnosis #EM ... #Peds #Crying # ... Infant #Algorithm
Breast Discharge - Differential Diagnosis Algorithm High Prolactin + Normal TSH • Microprolactinoma • Steroid Hormone Intake
Breast Discharge ... Differential Diagnosis Algorithm ... Contraceptive Pill/Patch/Ring ... #Endocrinology ... #Causes
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 ... varying degrees ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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