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diagnosis differential signs 21hydroxylasedeficiency 21ohd addisons adrenal adult distress dyspnea genetics hyponatremia insufficiency management neonatal nephrology pathophysiology pheochromocytoma primary respiratory
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 ... respiratory #distress #causes
Causes of Pediatric Wheezing - Differential Diagnosis Algorithm CXR Abnormal: • Pulmonary Sequestration • Congenital Adenoid Cystic
Causes of Pediatric ... Abnormal: • Pulmonary ... Endobronchial Disease ... #Causes #Peds # ... Pediatrics #Pulmonary
Pediatric Dyspnea - Differential Diagnosis Algorithm Stridor: • Croup • Foreign Body • Tracheitis • Epiglottitis •
Pediatric Dyspnea ... Body • Heart Disease ... Ketoacidosis • Pulmonary ... #Causes #Peds # ... Pediatrics
Hyponatremia - Differential Diagnosis Algorithm Hypovolemic - Give volume Hypervolemic (Edematous) - Look for and treat underlying cause
Differential Diagnosis Algorithm ... treat underlying cause ... Pulmonary Diseases ... , CNS Disease, Meds ... CKD, Thiazides, Hypothyroidism
Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
Insufficiency Addison's Disease ... Lymphoma Metastatic Disease ... disorder - Primary hypothyroidism ... #endocrinology ... #diagnosis #signs
Hyperthyroidism Overview Clinical Manifestation of Hyperthyroidism: • Fatigue • Weight loss • Heat intolerance • Depression, nervousness
goiter (Graves' disease ... TRAb) if Graves' disease ... #causes #diagnosis ... #differential #endocrinology ... #signs #symptoms
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... • Cushing's Disease ... Dwarfism) • Hypothyroidism ... #endocrinology ... #causes #pediatrics
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 ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Pheochromocytoma - Diagnosis and Management Summary 10 percent rule = 10% of pheochromocytomas are extra-adrenal, multiple, bilateral,
bilateral, malignant, pediatric ... and Signs: 50% ... and signs: • ... may present with pulmonary ... Treatment • Operable disease
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