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diagnosis nicu infant newborn complications diabetes diabetic gestational idm iem inbornerrors management maternal metabolism mother obgyn obstetrics table 21hydroxylasedeficiency 21ohd
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Differential #Neonatology ... #Peds #Pediatrics
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 ... InbornErrors #Metabolism #Neonatology ... #Peds #Pediatrics ... #Table #NICU #Genetics
Characteristic features of the rash are: -Rough texture (like sandpaper) -Worse in the skin folds e.g. groin, axilla,
#Dermatology #Peds ... #Pediatrics #SkinRash ... #ScarletFever # ... Trunk #Arms
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
complications - pathophysiology ... Diabetic #Mother #Pediatrics ... #Neonatology #IDM ... OBGYN #Diagnosis #Pathophysiology ... Complications #Peds
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
Diabetic #Mother #Pediatrics ... #Neonatology #IDM ... OBGYN #Diagnosis #Pathophysiology ... Complications #Peds
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... management #cardiology #peds ... #pediatrics #treatment
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
paediatrician or geneticist ... briefly when the trunk ... #Examination #Peds ... #Pediatrics #Diagnosis
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