Barter Syndrome classification: Difference between revisions
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*Bartter syndrome types 1, 2, and 4 present at a younger age. They present with symptoms, often quite severe in the neonatal period. | *Bartter syndrome types 1, 2, and 4 present at a younger age. They present with symptoms, often quite severe in the neonatal period. | ||
*Bartter Syndrome type 3 also called classic Bartter Syndrome present later in life and maybe sporadically asymptomatic or mildly symptomatic.<ref name="pmid22282380">{{cite journal| author=Fremont OT, Chan JC| title=Understanding Bartter syndrome and Gitelman syndrome. | journal=World J Pediatr | year= 2012 | volume= 8 | issue= 1 | pages= 25-30 | pmid=22282380 | doi=10.1007/s12519-012-0333-9 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22282380 }} </ref> | *Bartter Syndrome type 3 also called classic Bartter Syndrome present later in life and maybe sporadically asymptomatic or mildly symptomatic.<ref name="pmid22282380">{{cite journal| author=Fremont OT, Chan JC| title=Understanding Bartter syndrome and Gitelman syndrome. | journal=World J Pediatr | year= 2012 | volume= 8 | issue= 1 | pages= 25-30 | pmid=22282380 | doi=10.1007/s12519-012-0333-9 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22282380 }} </ref> | ||
==References== |
Revision as of 19:09, 28 July 2020
- Bartter Syndrome can be classified into four different types based on severity and age of onset.[1]
- Bartter syndrome type 1
- Bartter syndrome type 2
- Bartter syndrome type 3
- Bartter syndrome type 4
- Bartter syndrome types 1, 2, and 4 present at a younger age. They present with symptoms, often quite severe in the neonatal period.
- Bartter Syndrome type 3 also called classic Bartter Syndrome present later in life and maybe sporadically asymptomatic or mildly symptomatic.[1]
References
- ↑ 1.0 1.1 Fremont OT, Chan JC (2012). "Understanding Bartter syndrome and Gitelman syndrome". World J Pediatr. 8 (1): 25–30. doi:10.1007/s12519-012-0333-9. PMID 22282380.