2 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Labia major & minor ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
C.diff - Clostridioides Difficile Infection (CDI) - Diagnosis and Management - GrepMed Handbook

Clinical Presentation + Progression:
C.diff - Clostridioides ... Diagnosis and Management ... Perforation) Pathophysiology ... ciab549 #CDI #Cdiff ... #treatment #infectiousdiseases