Bartter syndrome differential diagnosis
|
Bartter syndrome Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Bartter syndrome differential diagnosis On the Web |
|
American Roentgen Ray Society Images of Bartter syndrome differential diagnosis |
|
Risk calculators and risk factors for Bartter syndrome differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Tayyaba Ali, M.D.[2]
Overview
Differentiating Bartter syndrome from other Diseases
Bartter syndrome diagnosis should be differentiated from other diseases manifesting with hypokalemia, normal to low blood pressure, and hypochloremic metabolic alkalosis.[1]
| Disease | Findings |
|---|---|
| Gitelman syndrome |
|
| Diuretic abuse |
|
| Cyclical vomiting |
|
| Hyperprostaglandin E syndrome |
|
| Familial hypomagnesemia with hypercalciuria/nephrocalcinosis |
|
| Cystic fibrosis |
|
| Gullner syndrome - Familial hypokalemic alkalosis with proximal tubulopathy |
|
| Mineralocorticoid excess |
|
| Activating mutations of the CaSR calcium-sensing receptor |
|
| Hypomagnesemia |
|
| Congenital chloride diarrhea |
|
| Hypochloremic alkalosis |
|
| Hypokalemia |
|
References
- ↑ Gitelman HJ, Graham JB, Welt LG (1966). "A new familial disorder characterized by hypokalemia and hypomagnesemia". Trans Assoc Am Physicians. 79: 221–35. PMID 5929460.
- ↑ Scognamiglio R, Negut C, Calò LA (2007). "Aborted sudden cardiac death in two patients with Bartter's/Gitelman's syndromes". Clin Nephrol. 67 (3): 193–7. doi:10.5414/cnp67193. PMID 17390745.
- ↑ Urbanová M, Reiterová J, Stěkrová J, Lněnička P, Ryšavá R (2011). "DNA analysis of renal electrolyte transporter genes among patients suffering from Bartter and Gitelman syndromes: summary of mutation screening". Folia Biol (Praha). 57 (2): 65–73. PMID 21631963.