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pediatrics diagnosis algorithm cardiology causes differential management endocrinology genetics treatment 21hydroxylasedeficiency 21ohd adrenal anatomy anomalous arteriosus baby blue cah cardiomyopathy
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
various types of congenital ... comparison #treatment #Peds ... Endocrinology #Adrenal #pathophysiology
Diagnostic algorithm for a child or adolescent with suspected pulmonary hypertension. CHD, congenital heart disease; CPET,
with suspected pulmonary ... CHD, congenital ... thromboembolic pulmonary ... HPAH, hereditary pulmonary ... #Diagnosis #Peds
Causes of Pediatric Wheezing - Differential Diagnosis Algorithm CXR Abnormal: • Pulmonary Sequestration • Congenital Adenoid Cystic
Abnormal: • Pulmonary ... Sequestration • Congenital ... Algorithm #Causes #Peds ... #Pediatrics #Pulmonary
Undifferentiated critical congenital heart disease: Patterns of Presentation Pink baby: • Presents at 1-6 mo
Undifferentiated critical congenital ... if cardiac or pulmonary ... annyoungMD #Congenital ... Blue #Gray #Baby #Peds
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Total Anomalous Pulmonary ... Classification • Pathophysiology ... Total #Anomalous #Pulmonary ... management #cardiology #peds
Causes of Cyanosis in the Newborn - Differential Diagnosis Algorithm Peripheral Only: • Poor Perfusion • Acrocyanosis Hemoglobinopathy:
Hemoglobinopathy: • Congenital ... Total Anomalous Pulmonary ... Algorithm #Causes #Peds
Truncus Arteriosus • Basic Information • Embryology • Associated anomalies • Pathophysiology/Presentation • Pre-operative management •
anomalies • Pathophysiology ... Cardiomegaly, increased pulmonary ... management #cardiology #peds
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Diagnosis Algorithm Congenital ... Neurologic Anomaly • Pulmonary ... Algorithm #Causes #Peds
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
sleep apnea, cor pulmonale ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
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