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Case Reports

. 2019 Aug;34(8):1375-1377.

doi: 10.1007/s00467-019-04217-7. Epub 2019 Mar 12.

Nephrotic syndrome and mitochondrial disorders: answers

Julie Bernardor¹, Camille Faudeux¹, Anabelle Chaussenot², Corinne Antignac^{3

4}, Alice Goldenberg⁵, Marie Claire Gubler³, Nicole Wagner⁶, Etienne Bérard⁷

Affiliations

Affiliations

¹ Unité de néphrologie pédiatrique, CHU de Nice - Hôpital Archet, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France.
² Service de génétique médicale, CHU de Nice - Hôpital Archet 2, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France.
³ Laboratoire des maladies rénales héréditaires 1 - INSERM UMR S1163, Institut Imagine, 24 boulevard du Montparnasse, 75015, Paris, France.
⁴ Department of Genetics, Reference center for Hereditary Kidney Diseases (MARHEA), Assistance Publique - Hôpitaux de Paris, Necker Hospital, 75015, Paris, France.
⁵ Unité de génétique clinique - CHU de Rouen, 1 Rue de Germont, 76031, Rouen Cedex, France.
⁶ CNRS, INSERM, iBV, Université Côte d'Azur, 06107, Nice, France.
⁷ Unité de néphrologie pédiatrique, CHU de Nice - Hôpital Archet, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France. berard.e@chu-nice.fr.

PMID: 30863911
DOI: 10.1007/s00467-019-04217-7

Case Reports

Nephrotic syndrome and mitochondrial disorders: answers

Julie Bernardor et al. Pediatr Nephrol. 2019 Aug.

. 2019 Aug;34(8):1375-1377.

doi: 10.1007/s00467-019-04217-7. Epub 2019 Mar 12.

Authors

Julie Bernardor¹, Camille Faudeux¹, Anabelle Chaussenot², Corinne Antignac^{3

4}, Alice Goldenberg⁵, Marie Claire Gubler³, Nicole Wagner⁶, Etienne Bérard⁷

Affiliations

¹ Unité de néphrologie pédiatrique, CHU de Nice - Hôpital Archet, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France.
² Service de génétique médicale, CHU de Nice - Hôpital Archet 2, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France.
³ Laboratoire des maladies rénales héréditaires 1 - INSERM UMR S1163, Institut Imagine, 24 boulevard du Montparnasse, 75015, Paris, France.
⁴ Department of Genetics, Reference center for Hereditary Kidney Diseases (MARHEA), Assistance Publique - Hôpitaux de Paris, Necker Hospital, 75015, Paris, France.
⁵ Unité de génétique clinique - CHU de Rouen, 1 Rue de Germont, 76031, Rouen Cedex, France.
⁶ CNRS, INSERM, iBV, Université Côte d'Azur, 06107, Nice, France.
⁷ Unité de néphrologie pédiatrique, CHU de Nice - Hôpital Archet, 151 Route de Saint-Antoine de Ginestière, B.P. 23079, 06202, Nice Cedex 3, France. berard.e@chu-nice.fr.

PMID: 30863911
DOI: 10.1007/s00467-019-04217-7

No abstract available

Keywords: Cardiomyopathy; Child; Congenital nephrotic syndrome (CNF); Mitochondrial disorder; NPHS1 mutation.

PubMed Disclaimer

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