3080 results
Causes of Hyperkalemia

Hyperkalemia is caused by excess potassium intake, impaired potassium excretion, or transcellular shifts. The
Causes of Hyperkalemia ... Hyperkalemia is caused ... impaired renal function ... rarely the sole cause ... #Differential #Causes
Causes of Pediatric Constipation - Differential Diagnosis Algorithm
Dietary / Functional:
 • Insufficient Volume / Bulk
Neurologic:
 •
Causes of Pediatric ... Algorithm Dietary / Functional ... Fibrosis Dietary/Functional ... Diagnosis #Algorithm #Causes
Approach to Nausea / Vomiting - Differential Diagnosis Framework
 • Gastrointestinal 
    -
Approach to Nausea ... Disorders • Other Causes ... Genitourinary • Functional ... /AnthonyXuMD #Nausea
The 9 Ds of Weight loss in the Elderly
 - Dementia
 - Depression
 - Disease (acute
- Dysfunction (functional ... Diagnosis #Geriatrics #Causes
Amenorrhea - Differential Diagnosis Algorithm
Elevated FSH
 • Premature Ovarian Failure
 • Menopa use
 • Spontaneous
Bleed With
Hyperprolactinemia Organic Cause ... Challenge • Functional ... endocrinology #causes
Causes of Primary and Functional Mitral Regurgitation (MR) 
Causes of primary mitral regurgitation
 - Rheumatic heart
Causes of Primary ... and Functional ... Regurgitation (MR) Causes ... Causes of functional ... #Primary #Functional
Torsades de Pointes (TdP): Pathogenesis and Clinical Findings

Polymorphic ventricular tachycardia initiated by PVC in the setting
maintained by functional ... pathophysiology #cardiology #causes
Oropharyngeal and Esophageal Causes of Dysphagia - Differential Diagnosis
Oropharyngeal Dysphagia
 • Neuromuscular causes: CVA/CNS tumor/ALS, Parkinson's,
and Esophageal Causes ... Neuromuscular causes ... • Structural causes ... Neuromuscular causes ... sclerosis - Functional
Iron Deficiency in Heart Failure
Pathophysiology:
Chronic heart failure leads to an increase in inflammatory cytokines → Inflammation
→ Inflammation causes ... with TSAT <20% (functional ... endpoint of all-cause
Marfan Syndrome - Signs and Symptoms

- Caused by mutations in the fibrillin-1 (FBN1) Gene (chromosome 15)
-
Symptoms - Caused ... Abnormal fibrillin function