Literature DB >> 22707176

Bartter syndrome and growth hormone deficiency: three cases.

Mithat Buyukcelik1, Mehmet Keskin2, Beltinge Demircioglu Kilic3, Yilmaz Kor2, Ayse Balat3.   

Abstract

BACKGROUND: Bartter syndrome is a rare autosomal recessive disorder characterized by hypokalemia, salt loss, and metabolic alkalosis. Short stature is one of the clinical manifestations in these children. Although polyuria, polydipsia, hypokalemia, and salt loss may be responsible for growth retardation, the exact pathogenesis of short stature in Bartter syndrome is not known. CASE DIAGNOSIS AND TREATMENT: In this study, we present three children diagnosed as having Bartter syndrome with short stature and growth hormone (GH) deficiency. After recombinant human growth hormone therapy (rhGH), their growth velocities were improved.
CONCLUSIONS: These results indicate that GH deficiency may contribute to short stature in children with Bartter syndrome, and rhGH therapy would be an excellent adjunctive treatment for short children with this syndrome whose condition is resistant to conventional therapies in terms of growth.

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Year:  2012        PMID: 22707176     DOI: 10.1007/s00467-012-2212-y

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  20 in total

1.  Bartter's syndrome with impairment of growth hormone secretion.

Authors:  L A Boer; G Zoppi
Journal:  Lancet       Date:  1992-10-03       Impact factor: 79.321

2.  Bartter's syndrome and growth hormone replacement.

Authors:  N Itami; N Satake; M Yoshida; E Ohshika; Y Koga
Journal:  Lancet       Date:  1992-12-05       Impact factor: 79.321

3.  Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.

Authors:  Martin Konrad; Martin Vollmer; Henny H Lemmink; Lambertus P W J VAN DEN Heuvel; Nikola Jeck; Rosa Vargas-Poussou; Alicia Lakings; Rainer Ruf; Georges Deschênes; Corinne Antignac; Lisa Guay-Woodford; Nine V A M Knoers; Hannsjörg W Seyberth; Delphine Feldmann; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2000-08       Impact factor: 10.121

4.  [Exchangeable electrolytes, glycoregulation and growth hormone in one case of Bartter's syndrome (author's transl)].

Authors:  J Lefebvre; A Racadot; P Dequiedt; M Linquette
Journal:  Ann Endocrinol (Paris)       Date:  1977       Impact factor: 2.478

Review 5.  Bartter syndromes and other salt-losing tubulopathies.

Authors:  Robert Kleta; Detlef Bockenhauer
Journal:  Nephron Physiol       Date:  2006-06-19

Review 6.  Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes.

Authors:  A J Shaer
Journal:  Am J Med Sci       Date:  2001-12       Impact factor: 2.378

7.  Bartter syndrome. Typical facies and normal plasma volume.

Authors:  T James; N H Holland; D Preston
Journal:  Am J Dis Child       Date:  1975-10

Review 8.  Longitudinal growth in chronic hypokalemic disorders.

Authors:  Helena Gil-Peña; Natalia Mejia; Oscar Alvarez-Garcia; Vanessa Loredo; Fernando Santos
Journal:  Pediatr Nephrol       Date:  2009-11-10       Impact factor: 3.714

9.  Alterations of growth plate and abnormal insulin-like growth factor I metabolism in growth-retarded hypokalemic rats: effect of growth hormone treatment.

Authors:  Helena Gil-Peña; Enrique Garcia-Lopez; Oscar Alvarez-Garcia; Vanessa Loredo; Eduardo Carbajo-Perez; Flor A Ordoñez; Julian Rodriguez-Suarez; Fernando Santos
Journal:  Am J Physiol Renal Physiol       Date:  2009-07-08

10.  Growth hormone (GH) receptor and GH-binding protein deficiency in the growth failure of potassium-depleted rats.

Authors:  Z Hochberg; T Amit; A Flyvbjerg; I Dørup
Journal:  J Endocrinol       Date:  1995-11       Impact factor: 4.286

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  9 in total

1.  Gitelman syndrome combined with complete growth hormone deficiency.

Authors:  Se Ra Min; Hyun Seok Cho; Jeana Hong; Hae Il Cheong; Sung Yeon Ahn
Journal:  Ann Pediatr Endocrinol Metab       Date:  2013-03-31

2.  Clinical and Genetic Spectrum of Bartter Syndrome Type 3.

Authors:  Elsa Seys; Olga Andrini; Mathilde Keck; Lamisse Mansour-Hendili; Pierre-Yves Courand; Christophe Simian; Georges Deschenes; Theresa Kwon; Aurélia Bertholet-Thomas; Guillaume Bobrie; Jean Sébastien Borde; Guylhène Bourdat-Michel; Stéphane Decramer; Mathilde Cailliez; Pauline Krug; Paul Cozette; Jean Daniel Delbet; Laurence Dubourg; Dominique Chaveau; Marc Fila; Noémie Jourde-Chiche; Bertrand Knebelmann; Marie-Pierre Lavocat; Sandrine Lemoine; Djamal Djeddi; Brigitte Llanas; Ferielle Louillet; Elodie Merieau; Maria Mileva; Luisa Mota-Vieira; Christiane Mousson; François Nobili; Robert Novo; Gwenaëlle Roussey-Kesler; Isabelle Vrillon; Stephen B Walsh; Jacques Teulon; Anne Blanchard; Rosa Vargas-Poussou
Journal:  J Am Soc Nephrol       Date:  2017-04-05       Impact factor: 10.121

Review 3.  Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance.

Authors:  Laura Florea; Lavinia Caba; Eusebiu Vlad Gorduza
Journal:  Front Pediatr       Date:  2022-06-03       Impact factor: 3.569

4.  Identification of compound heterozygous KCNJ1 mutations (encoding ROMK) in a kindred with Bartter's syndrome and a functional analysis of their pathogenicity.

Authors:  Shalabh Srivastava; Dimin Li; Noel Edwards; Ann-M Hynes; Katrina Wood; Mohamed Al-Hamed; Anna C Wroe; David Reaich; Shabbir H Moochhala; Paul A Welling; John A Sayer
Journal:  Physiol Rep       Date:  2013-11-19

5.  Clinical and diagnostic features of Bartter and Gitelman syndromes.

Authors:  Patrick R Walsh; Yincent Tse; Emma Ashton; Daniela Iancu; Lucy Jenkins; Marc Bienias; Robert Kleta; William Van't Hoff; Detlef Bockenhauer
Journal:  Clin Kidney J       Date:  2017-11-10

6.  A novel CLCNKB mutation in a Chinese girl with classic Bartter syndrome: a case report.

Authors:  Binlu Zhu; Hong Jiang; Meiling Cao; Xueqi Zhao; Hongkun Jiang
Journal:  BMC Med Genet       Date:  2019-08-13       Impact factor: 2.103

7.  Gitelman syndrome combined with growth hormone deficiency: Three cases report.

Authors:  Ke Huang; Yang-Li Dai; Jian-Wei Zhang; Li Zhang; Wei Wu; Guan-Ping Dong; Rahim Ullah; Yue Fei; Jun-Fen Fu
Journal:  Medicine (Baltimore)       Date:  2019-10       Impact factor: 1.889

8.  Classic Bartter syndrome complicated with profound growth hormone deficiency: a case report.

Authors:  Masanori Adachi; Toshihiro Tajima; Koji Muroya; Yumi Asakura
Journal:  J Med Case Rep       Date:  2013-12-30

Review 9.  Bartter and Gitelman syndromes: Questions of class.

Authors:  Martine T P Besouw; Robert Kleta; Detlef Bockenhauer
Journal:  Pediatr Nephrol       Date:  2019-10-29       Impact factor: 3.714

  9 in total

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