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Literature DB >> 2386386

Pseudo-Bartter's syndrome in cystic fibrosis.

J D Kennedy¹, R Dinwiddie, C Daman-Willems, M J Dillon, D J Matthew.

Abstract

Seven cases of cystic fibrosis complicated by chronic salt depletion and failure to thrive were studied. After replacement of the salt deficit, the metabolic abnormalities resolved, and weight gain was rapid. This should be considered as a differential diagnosis in children who have been diagnosed as having cystic fibrosis, but who fail to thrive despite standard treatment.

Entities: Chemical Disease Species

Mesh：

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Year: 1990 PMID： 2386386 PMCID： PMC1792454 DOI： 10.1136/adc.65.7.786

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

4 in total

1. Studies in the physiology of sweating in cystic fibrosis. II. Elevated night sweating rates.

Authors: M S SIBINGA; G J BARBERO
Journal: Arch Dis Child Date: 1961-10 Impact factor: 3.791

2. Elevated sweat potassium, hyperaldosteronism and pseudo-Bartter's syndrome: a spectrum of disorders associated with cystic fibrosis.

Authors: J Devlin; N S Beckett; T J David
Journal: J R Soc Med Date: 1989 Impact factor: 5.344

3. Metabolic alkalosis and salt depletion in cystic fibrosis.

Authors: S N Arvanitakis; C C Lobeck
Journal: J Pediatr Date: 1973-03 Impact factor: 4.406

4. Bartter's syndrome: 10 cases in childhood. Results of long-term indomethacin therapy.

Authors: M J Dillon; V Shah; M D Mitchell
Journal: Q J Med Date: 1979-07

4 in total

13 in total

Review 1. Cystic fibrosis: yesterday, today and tomorrow.

Authors: R Dinwiddie
Journal: J R Soc Med Date: 1991 Impact factor: 5.344

2. Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome.

Authors: Natsuki Matsunoshita; Kandai Nozu; Masahide Yoshikane; Azusa Kawaguchi; Naoya Fujita; Naoya Morisada; Shingo Ishimori; Tomohiko Yamamura; Shogo Minamikawa; Tomoko Horinouchi; Keita Nakanishi; Junya Fujimura; Takeshi Ninchoji; Ichiro Morioka; Hiroaki Nagase; Mariko Taniguchi-Ikeda; Hiroshi Kaito; Kazumoto Iijima
Journal: J Hum Genet Date: 2018-05-30 Impact factor: 3.172

Review 3. Threading through the mizmaze of Bartter syndrome.

Authors: Willem Proesmans
Journal: Pediatr Nephrol Date: 2006-05-16 Impact factor: 3.714

4. Clinical quiz. Sweat test indicates cystic fibrosis in a child with sweat sodium of 99 mmol/l and sweat chloride of 139 mmol/l.

Authors: M C English
Journal: Pediatr Nephrol Date: 1993-02 Impact factor: 3.714

5. Metabolic alkalosis with hypo-electrolytaemia or pseudo-Bartter syndrome as a presentation of cystic fibrosis in infancy. Discription of three cases.

Authors: H Escobar Castro; E Medina; E Kirchschläger; C Camarero; L Suarez
Journal: Eur J Pediatr Date: 1995-10 Impact factor: 3.183

Pseudo-Bartter's syndrome in cystic fibrosis.

1. Studies in the physiology of sweating in cystic fibrosis. II. Elevated night sweating rates.

2. Elevated sweat potassium, hyperaldosteronism and pseudo-Bartter's syndrome: a spectrum of disorders associated with cystic fibrosis.

3. Metabolic alkalosis and salt depletion in cystic fibrosis.

4. Bartter's syndrome: 10 cases in childhood. Results of long-term indomethacin therapy.

Review 1. Cystic fibrosis: yesterday, today and tomorrow.

2. Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome.

Review 3. Threading through the mizmaze of Bartter syndrome.

4. Clinical quiz. Sweat test indicates cystic fibrosis in a child with sweat sodium of 99 mmol/l and sweat chloride of 139 mmol/l.

5. Metabolic alkalosis with hypo-electrolytaemia or pseudo-Bartter syndrome as a presentation of cystic fibrosis in infancy. Discription of three cases.

Review 6. Electrolyte abnormalities in cystic fibrosis: systematic review of the literature.

7. Chloride deficiency as a presentation or complication of cystic fibrosis.

Review 8. CFTR and defective endocytosis: new insights in the renal phenotype of cystic fibrosis.

9. Recurrent Metabolic Alkalosis in a Cystic Fibrosis Patient: Coexistence with Congenital Chloride Diarrhea.

10. Metabolic alkalosis in adults with stable cystic fibrosis.