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peds diabetes differential endocrinology gestational idm maternal mother neonatology newborn nicu obgyn obstetrics 21hydroxylasedeficiency 21ohd adrenal algorithm alzheimersdisease antenatal cah
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... Mother - complications ... - pathophysiology ... #Pediatrics #Neonatology ... #NICU #OBGYN #Diagnosis
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
algorithm #Infant ... #Pediatrics #Neonatology ... #NICU #OBGYN #Diagnosis ... #Pathophysiology ... #Maternal #Complications
Comparison of Causes of Salt-Wasting in Infancy - PHA 1 - PHA 3 - 21-OH CAH
Comparison of Causes ... Salt-Wasting in Infancy ... #Comparison #Causes ... #differential #diagnosis ... #pediatrics #nephrology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #pediatrics #CongenitalAdrenalHyperplasia ... #diagnosis #comparison ... Endocrinology #Adrenal #pathophysiology
Fecal Incontinence - Pathogenesis and Complications Continence mechanisms are impaired • Local neuronal damage • External and
Pathogenesis and Complications ... mechanisms are intact ... Diabetes) • Altered ... #Incontinence #geriatrics ... #pathophysiology
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
Preterm Infant Complications ... - Differential Diagnosis ... #Complications ... #Causes #Peds # ... Pediatrics
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Alzheimer's (99% of cases ... Alzheimer's (1% of cases ... Signs / Symptoms / Complications ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
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