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diagnosis pediatrics management differential treatment cardiology causes 21hydroxylasedeficiency 21ohd acromegaly congenital diagram fallot fontan hemoptysis kleefstra lung neurology patientinfo praderwilli
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... Syndromes • “Pink ... management #cardiology #peds
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... sleep apnea, cor pulmonale ... #genetics #pathophysiology ... #peds #pediatrics
Hemoptysis - Differential Diagnosis Framework Airways: • Bronchitis • Bronchiectasis • Malignancy: Primary bronchogenic CA, Endobronchial
westermani, PNA, Lung abscess ... Pneumonitis, GPA, Behcet syndrome ... , Idiopathic pulmonary ... hemosiderosis • Genetic ... Osler-Weber-Rendu syndrome
Lung Abscess - Diagnosis and Management Summary Lung Abscess Etiology: • Necrosis of lung parenchyma by a
Lung Abscess - Diagnosis ... Summary Lung Abscess ... Pathophysiology ... Coccidioides • Parasite ... #pulmonary #differential
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Weakness - Differential Diagnosis Framework Approach To Weakness: • Non-neuromuscular disorder (Cardiac, pulmonary etc) • CNS ->
disorder (Cardiac, pulmonary ... • Acute stroke syndromes ... Infectious: Brain abscess ... Paraneoplastic syndrome ... Malignancy-associated myositis • Genetic
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
malignancy Pathophysiology ... phenytoin, minoxidil), genetic ... Beckwith Wiedemann syndrome ... Diagnosis #Management #Endocrinology ... #Treatment #Pathophysiology
Kleefstra Syndrome is a rare genetic disorder, caused by a EHMT-1 gene deletion or mutation. Most kids
Kleefstra Syndrome ... is a rare genetic ... with Kleefstra Syndrome ... it difficult to assess ... #PatientInfo #Peds
Fontan Procedure Schematic A Fontan is done in most children (approximately 90%) who effectively have a single
or a congenital syndrome ... flow into the pulmonary ... flow into the pulmonary ... congenital #Cardiology #Peds ... #Pediatrics #Pathophysiology
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