13 results
diagnosis pathophysiology algorithm signs causes differential disease genetics management newborn 21hydroxylasedeficiency 21ohd chagas childhood depressed diagram endocrinology evaluation examination failuretothrive
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Ventricular septal defect ... Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms
Causes of Depressed / Lethargic Newborn - Differential Diagnosis Algorithm Maternal Related: • Drugs (Ex. SSRI) •
Hypertension Congenital ... Heart Defect Respiratory ... Respiratory Distress Syndrome ... Algorithm #Causes #Peds ... #Pediatrics
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
febrile vasculitic syndrome ... Affects children ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
Algorithm for the Evaluation and Management of Suspected Congenital Heart Disease in Neonates Neonates with undiagnosed congenital
Management of Suspected Congenital ... with undiagnosed congenital ... with nonspecific symptoms ... Neonates #Neonatal #Peds ... #Pediatrics #Cardiology
Pediatric Inflammatory Multisystem Syndrome Temporally associated with SARS-CoV-2 infection (PIMS-TS) #PIMSTS #Pediatrics #Inflammatory #Multisystem #Syndrome #Peds #Signs
Pediatric Inflammatory ... Multisystem Syndrome ... PIMS-TS) #PIMSTS #Pediatrics ... #Multisystem #Syndrome ... #Peds #Signs #Symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... Signs/Symptoms ... pathophysiology #peds ... #pediatrics
Congenital Long QT Syndrome: Illness Script Who? - Kids or young adults, usually < 30 - high
Congenital Long ... QT Syndrome: Illness ... live births Symptoms ... #LongQT #Syndrome ... #Diagnosis #Cardiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
hemorrhagic rash; symptoms ... organ ischemia -> Congenital ... cataracts, cardiac defects ... #Immunization #peds ... #pediatrics #pathophysiology
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... are observed for signs ... for any midline defects ... #Examination #Peds ... #Pediatrics #Diagnosis
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