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peds diagnosis genetics endocrinology neonatology nicu causes differential iem inbornerrors metabolism table 21hydroxylasedeficiency 21ohd adrenal antenatal cah comparison complications congenitaladrenalhyperplasia
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
congenital adrenal hyperplasia ... #CAH #algorithm ... #causes #pediatrics ... Endocrinology #Adrenal #pathophysiology
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... connections and pathophysiology ... of information: Pediatrics ... , UpToDate #Pediatrics ... #Diagnosis #Algorithm
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Neonatology #Peds #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Complications: • Gonadal hypoplasia ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... Congenital Adrenal Hyperplasia ... Differential #Diagnosis #Algorithm ... endocrinology #causes #pediatrics
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... Diabetic #Mother #Pediatrics ... OBGYN #Diagnosis #Pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
congenital adrenal hyperplasia ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
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