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21hydroxylasedeficiency 21ohd adrenal algorithm ascorbicacid cah comparison congenitaladrenalhyperplasia genetics management nutrition scurvy treatment vitaminc
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #diagnosis #comparison ... #treatment #Peds ... #Endocrinology ... #Adrenal #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 ... deficiencies present in infants ... Signs/Symptoms/Complications ... #genetics #endocrinology ... #peds #pediatrics
Scurvy (Vitamin C Deficiency) - Diagnosis and Management Vitamin C is required for hydroxylation of proline residues
Deficiency) - Diagnosis ... eating habits • Infants ... Psychiatric symptoms ... nonimmune hemolysis MSK ... , or any other cause
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