19 results
diagnosis differential pediatrics management neurology physicalexam symptoms 21hydroxylasedeficiency 21ohd abnormal abnormalities adhesivecapsulitis agammaglobulinemia als alte ammonia amyotrophic breathing brudzinskis brue
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Differential Diagnosis Algorithm ... Nervous System - Decreased ... #Causes #Peds #
Hypochloremia - Differential Diagnosis Algorithm Cause - Decreased Intake: • Low salt in diet • Exclusive D5W
Differential Diagnosis Algorithm ... Cause - Decreased ... - Gitelman SIGNS ... acidosis - Cl⁻ decrease ... #Pathophysiology
Pediatric Dyspnea - Differential Diagnosis Algorithm Stridor: • Croup • Foreign Body • Tracheitis • Epiglottitis •
Differential Diagnosis Algorithm ... Foreign Body Decreased ... Body • Heart Disease ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
Causes of Iron Deficiency - Differential Diagnosis Algorithm • Blood loss: GI (cancer, ulcer, IBD), GU
Causes of Iron Deficiency ... Differential Diagnosis Algorithm ... intake for needs: Infancy ... MALABSORPTION • Decreased ... #Fe #algorithm
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Differential Diagnosis Algorithm ... Congenital Heart Disease ... Breathing • Apnea of Infancy ... #Causes #Peds #
Schematic representation of the major sources of ammonia production and its excretory pathway (GI = gastrointestinal,
although hepatic causes ... decompensated liver disease ... of ammonia and decreased ... Reye syndrome (Peds ... deficiency #Ammonia #Pathophysiology
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Passive neck flexion causes ... While the pathophysiology ... despite severe disease ... PhysicalExam #Pediatrics #Peds
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 X-Linked Agammaglobulinemia: Pathogenesis and clinical findings The epidemiology of this disease is 1/340,000 births and roughly double
epidemiology of this disease ... history of the disease ... Signs of immunodeficiency ... to produce all classes ... Agammaglobulinemia #XLinked #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
incomplete Kawasaki Disease ... Infants ≤6 months ... lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds
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