Types III and V typically occur later in childhood and cause milder symptoms, so they are considered to be classic Bartter syndrome. Type III may resemble Gitelman syndrome in some patients. ...

Bartter syndrome type 3 is the result of several structural variants in the genome. By using long-read sequencing, Janine Altmüller and her team from the Max Delbrück Center, the BIH and ...

Bartter syndrome type 3 is the result of several structural variants in the genome. By using long-read sequencing, Janine Altmüller and her team from the Max Delbrück Center, the BIH and University ...

Bartter syndrome is mainly divided into five sub-types. Mutations in the sodium chloride/potassium chloride cotransporter gene (SLC12A1) cause Type I. Mutations in the KCNJ1 gene cause Type II.

Diagnosis of Bartter syndrome is made with the use of a thorough clinical evaluation, blood tests, urine analysis, and ...

We treated a two-year-old girl who had Bartter's syndrome type II (body weight, 7.4 kg, which is below the 3rd percentile; length, 74 cm, which is also below the 3rd percentile) with a balanced ...

In a newly identified phenotype of antenatal Bartter's syndrome, both severe renal salt wasting and sensorineural deafness are present; it is called antenatal Bartter's syndrome with sensorineural ...

Type III Bartter syndrome (BS) (OMIM607364) is caused by mutations in the basolateral chloride channel ClC-Kb gene (CLCNKB). The CLCNKB gene is sometimes reported as having a large deletion ...

(HealthDay)—A mutation has been identified in MAGED2 that causes transient antenatal Bartter's syndrome, according to a study published online April 27 in the New England Journal of Medicine.

Bartter syndrome is a rare congenital renal tubular disorder causing an imbalance of potassium, sodium, chloride and calcium. It is classified into five types: (1) neonatal (Types I and II), (2 ...