9 results
Infant of a Diabetic Mother - complications - pathophysiology learning schema
Information source: UpToDate

#Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... Mother - complications ... - pathophysiology ... : UpToDate #Infant ... Diabetic #Mother #Pediatrics
gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
diabetes algorithm #Infant ... Diabetic #Mother #Pediatrics ... OBGYN #Diagnosis #Pathophysiology ... #Maternal #Complications
Comparison of Causes of Salt-Wasting in Infancy
 - PHA 1
 - PHA 3
 - 21-OH CAH
Salt-Wasting in Infancy ... CAH - X-Linked AHC ... Salt #Wasting #Infancy ... Comparison #Causes #differential ... #diagnosis #pediatrics
Fecal Incontinence - Pathogenesis and Complications
Continence mechanisms are impaired
 • Local neuronal damage
 • External and
Pathogenesis and Complications ... mechanisms are intact ... #Incontinence #geriatrics ... #pathophysiology
Classification of Pelvic Ring Fractures: Mechanisms, Clinical Features and Complications
 • Anterior Posterior Compression (APC) -
Clinical Features and Complications ... posterior Sl ligaments intact ... Grade 3 - APC 2 ... MSK #diagnosis #complications ... #pathophysiology
Widened Pulse Pressure - Differential Diagnosis and Pathophysiology

Pulse pressure is the difference between the systolic blood
Diagnosis and Pathophysiology ... pressure and the diastolic ... Blood Pressure - Diastolic ... • Sepsis Complications ... #Diagnosis #Pathophysiology
Mechanical Complications in Acute Myocardial Infarction
Acute LV/RV Dysfunction:
 • Regional wall motion, systolic and diastolic function,
Mechanical Complications ... , systolic and diastolic ... wall (inferior infarct ... cardionerds #Complications ... acuteMI #cardiology #differential
Preterm Infant Complications - Differential Diagnosis
Respiratory:
 • Transient Tachypnea of the Newborn (TTN)
 • Respiratory Distress
Preterm Infant Complications ... - Differential ... #Complications ... #Differential #Diagnosis ... #Causes #Peds #Pediatrics
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 ... endocrinology #peds #pediatrics