10 results
diagnosis management algorithm diabetes diabetic evaluation fever genetics gestational idm infant maternal mother neonatology newborn nicu obgyn obstetrics 21hydroxylasedeficiency 21ohd
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Diabetic Mother - complications ... - pathophysiology ... Diabetic #Mother #Pediatrics ... #Maternal #Complications ... #Peds #Newborn
Algorithm for the Evaluation of Pediatric Head Trauma (PECARN) - Need for Head CT #Diagnosis #Management
Evaluation of Pediatric ... Diagnosis #Management #EM ... #Peds #Trauma # ... PECARN #Algorithm #Ddxof
Rapid Pediatric Assessment Diagram: * Assessment of Appearance - Tone: Moves spontaneously, resists examination -
Rapid Pediatric ... Cyanosis #Diagnosis #EM ... #Peds #Rapid #Assessment ... Decompensated #Shock #Ddxof
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
Diabetic #Mother #Pediatrics ... OBGYN #Diagnosis #Pathophysiology ... #Maternal #Complications ... #Peds #Newborn
Pathophysiology Pediatric Fever #Pathophys #Peds #Fever #Ddxof
Pathophysiology ... Pediatric Fever ... #Pathophys #Peds ... #Fever #Ddxof
Evaluation and Management of Pediatric Fever #Diagnosis #Management #EM #Peds #Fever #Workup #Evaluation #Discharge #Admission #Algorithm
Management of Pediatric ... Diagnosis #Management #EM ... #Peds #Fever #Workup ... Admission #Algorithm #Ddxof
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Signs/Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
resolve by 72 hours Complications ... #OtitisMedia #pathophysiology ... symptoms #signs #peds ... #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Retinopathy of Prematurity: Pathogenesis and clinical findings Increased metabolic demand of growing eye -> Excessive VEGF production ->
-> Neovascular complications ... #Prematurity #peds ... #pediatrics #pathophysiology
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