24 results
differential algorithm management infant physicalexam symptoms complications constipation genetics geriatrics hematology nephrology newborn 21hydroxylasedeficiency 21ohd alte alzheimersdisease apgar assessment brudzinskis
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Signs/Symptoms ... delayed puberty -> Infertility ... #genetics #pathophysiology ... #peds #pediatrics
Causes of Pediatric Constipation - Differential Diagnosis Algorithm Dietary / Functional: • Insufficient Volume / Bulk Neurologic: •
Causes of Pediatric ... - Differential Diagnosis ... Volume / Bulk Neurologic ... Guillain-Barré Syndrome ... #Peds #Pediatrics
Pediatric Constipation - Differential Diagnosis Algorithm Dietary/Functional • lnsufficient Volume / Bulk Neurologic • Hirschsprung's Disease • Imperforate
Pediatric Constipation ... - Differential Diagnosis ... Guillan-Barré Syndrome ... #Algorithm #Causes ... #Peds
Newborn Assessment - APGAR Score Assessment of newborn vital signs following labor via a 10-point scale evaluated
newborn vital signs ... score remains low ... develop long-term neurologic ... #Diagnosis #Peds ... #Pediatrics #APGAR
Multi-System Inflammatory Syndrome in Children (MIS-C) vs. Kawasaki Disease CDC Case Definition for MIS-C; • < 21
Multi-System Inflammatory Syndrome ... Kawasaki Disease CDC Case ... Positive COVID testin now ... Kawasaki #Comparison #diagnosis ... #peds #pediatrics
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Causes of Sudden ... - Differential Diagnosis ... Arrhythmia • Neurologic ... Sudden Infant Death Syndrome ... #Peds #Pediatrics
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
- Differential Diagnosis ... Respiratory Distress Syndrome ... Enterocolitis (NEC) Neurologic ... #Causes #Peds # ... Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... endocrinology #peds ... #pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... - Differential Diagnosis ... Metabolism • Reye's Syndrome ... Disturbances Neurologic ... #Peds #Pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... meningitis, it has low ... #PhysicalExam #Pediatrics ... #Peds
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