14 results
management causes differential genetics signs syndrome 21hydroxylasedeficiency 21ohd alte antenatal aphasia brocas brue complications cop counseling cryptogenic decisionaid diabetes diabetic
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Arrhythmia • Neurologic ... Anomaly • Pulmonary ... #Diagnosis #Algorithm ... #Causes #Peds # ... Pediatrics
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children Urinary
Clinical Algorithm ... do not replace clinical ... #Diagnosis #Management ... #Peds #UrinaryTract ... #Pediatrics #Fever
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... #Infant #Diabetic ... #Mother #Pediatrics ... #Pathophysiology ... Complications #Peds
Causes of Pediatric Stridor - Differential Diagnosis Algorithm Present Since Infancy with No Respiratory Distress: • Laryngomalacia Present
Causes of Pediatric ... Algorithm Present ... Since Infancy with ... #Peds #Pediatrics ... #Pulmonary
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Syndrome Signs/Symptoms ... sleep apnea, cor pulmonale ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
- Differential Diagnosis ... Algorithm Cardiac ... Disturbances Neurologic ... Breathing • Apnea of Infancy ... #Peds #Pediatrics
Aphasia - Pathophysiology and Clinical Findings Broca's Aphasia - Expressive language impairment: non-Fluent - Sensory speech areas
Aphasia - Pathophysiology ... and Clinical Findings ... #diagnosis #signs ... #symptoms #Brocas ... #Wernickes #neurology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... #OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... if they have no clinical ... purposes of this algorithm ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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