pathophysiology ophthalmology slitlamp symptoms complications peds management obgyn genetics infant

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gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn

diabetes algorithm #Infant ... #Diagnosis #Pathophysiology ... #Maternal #Complications ... #Peds #Newborn ... #PatientInfo #Management

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

deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics

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