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diagnosis peds signs acutepe genetics management pathophysiology respiratory 21hydroxylasedeficiency 21ohd adult assessment breathing causes cirrhosis clinical dehydration differential distress effusion
Practical Pediatric Viral Rash Algorithm Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... Viral Rash Algorithm ... five days and no signs ... / symptoms of sepsis ... #Pediatrics #Peds
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... differential #neonatal #pediatrics ... #adult #peds #pulmonary
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
Evaluation #Assessment #Signs ... #Symptoms #PhysicalExam ... Diagnosis #Peds #Pediatrics
Hypothyroidism – symptoms and signs. Symptoms: Tiredness/malaise, Weight gain, Anorexia, Cold intolerance, Poor memory, Change in appearance, Depression, Poor libido,
Hypothyroidism – symptoms ... and signs. ... Symptoms: Tiredness ... #PhysicalExam # ... Endocrinology
Paradoxical Breathing on Physical Exam Paradoxical breathing is often a sign of breathing problems. It causes the
breathing is often a sign ... Paradoxical #Breathing #PhysicalExam ... clinical #video #pulmonary ... #peds #pediatrics
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 Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Extremities #PhysicalExam ... #Signs #Symptoms ... Dehydration #Peds #Pediatrics
Diagnostic Algorithm for Suspected Pulmonary Embolism Well's Criteria for PE • Clinical Signs and Symptoms of DVT
Diagnostic Algorithm ... for Suspected Pulmonary ... PE • Clinical Signs ... and Symptoms of ... AcutePE #Diagnosis #Algorithm
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... sleep apnea, cor pulmonale ... pathophysiology #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Pheochromocytoma - Diagnosis and Management Summary 10 percent rule = 10% of pheochromocytomas are extra-adrenal, multiple, bilateral,
bilateral, malignant, pediatric ... life • M=F Symptoms ... and Signs: 50% ... and signs: • ... may present with pulmonary
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