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diagnosis mri msk cardiology management knee peds treatment posterior pulmonary algorithm chf endocrinology heartfailure iem inbornerrors mass mediastinal metabolism middle
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the lab values table ... MetabolicEmergency #Genetics ... #Pathophysiology ... Diagnosis #Algorithm #Differential ... #Table #IEM #NICU
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Metabolism A table ... from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Neonatology #Peds #Pediatrics ... #Table #NICU #Genetics
Congestive Heart Failure - Causes, Pathophysiology and Differential Diagnosis • Dilated Cardiomyopathy • Hypertrophic Cardiomyopathy
, Pathophysiology ... and Differential ... Infiltrative • Genetic ... #Differential # ... Diagnosis #cardiology
Mediastinal masses are discussed in more detail in Mediastinal masses. Here is just a brief overview. #Diagnosis
Mediastinal masses ... in Mediastinal masses ... #Diagnosis #Radiology ... Mediastinal #Mass #Differential ... #Table #Anterior
Etiologies of Hypoaldosteronism Hyporeninemic Hypoaldosteronism (Low Renin, Low Aldosterone) - Diabetic Nephropathy - NSAIDs Non-Hyporeninemic Hypoaldosteronism (Normal
insufficiency - Critical ... illness - Genetic ... Hypoaldosteronism #Differential ... Aldosterone #Comparison #Table ... #Causes
Humeral Avulsion of the Inferior Glenohumeral Ligament (HAGL) • Imaging Findings: • Large defect of the
HAGL) can be a cause ... of anterior shoulder ... Differential diagnosis ... #mri #clinical ... #Radiology #diagnosis
Torsades de Pointes (TdP): Pathogenesis and Clinical Findings Polymorphic ventricular tachycardia initiated by PVC in the setting
Pathogenesis and Clinical ... TdP #Diagnosis #pathophysiology ... #cardiology #causes ... #differential
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
workup 1) Clinical ... Alzheimer - 1st cause ... hyperorality, - 25% genetic ... Dementia - 2nd cause ... MNCD #Dementia #Differential
Prior anterior glenohumeral joint dislocation with Hill-Sachs fracture and Perthes lesion Imaging Findings: • The arrow is
Case description ... surgical repair Differential ... Perthes #lesion #clinical ... #mri #clinical ... #Radiology #diagnosis
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