6 results
pediatrics diagnosis genetics 21hydroxylasedeficiency 21ohd anatomy cardiomyopathy chest circulation clinical cxr differential endocrinology falot fetal management peripartum praderwilli pressure pulse
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... hypothalamus =>Prader-Willi ... Signs/Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Tetralogy of Falot on Chest X-Ray Tetralogy of Falot comprises four defects - 1. Ventricular septal defect (VSD) 2.
boot shaped heart caused ... which is a common complication ... CXR #clinical #radiology ... #peds #pediatrics ... #cardiology #ToF
Widened Pulse Pressure - Differential Diagnosis and Pathophysiology Pulse pressure is the difference between the systolic blood
Diagnosis and Pathophysiology ... Physiologic Causes ... • Sepsis Complications ... Differential #Diagnosis #Pathophysiology ... #causes #cardiology
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Peripartum Cardiomyopathy - Summary 1. Definition • Towards the end of pregnancy to 5 months postpartum
exclude other causes ... Thromboembolic complications ... teratogenic GDMT meds ... diagnosis #management #cardiology
Fetal and Post Transition Circulation In the fetal circulatory system, oxygenated blood is delivered via the umbilical
oxygenated blood passes ... #Circulation #Pathophysiology ... #Cardiology #Anatomy ... #Peds #Pediatrics
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