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Antenatal Membranous Nephropathy and Type 2 (Axonal) Charcot-Marie-Tooth With Mutations in the Metallo-Membrane Endopeptidase Gene: A Call for Family Screening and Pharmacovigilance

Joëlle Nortier 1 Gauthier Remiche 2 Paul Delrée 3 Jeroen Nauta 4 Nicolette Notermans 5 Marina Vivarelli 6 Daria Diodato 6 Guilhem Solé 7 Hanna Debiec 8 Pierre Ronco 8
1 CHU - Centre Hospitalier Universitaire Brugmann [Bruxelles]
2 ULB - Hôpital Erasme [Bruxelles]
3 I.P.G. - Institut de Pathologie et Génétique [Gosselies]
4 Eramus MC-Sophia Children’s Hospital
5 University Medical Center [Utrecht]
6 Bambino Gesù Children’s Hospital [Rome, Italy]
7 Hôpital Pellegrin
8 Des Maladies Rénales Rares aux Maladies Fréquentes, Remodelage et Réparation
Keywords : congenital nephropathy maternofetal allo-immunization membranous nephropathy MME gene neprilysin neutral endopeptidase peripheral neuropathy
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Journal articles
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https://hal.sorbonne-universite.fr/hal-03333713
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Submitted on : Friday, September 3, 2021 - 10:50:15 AM
Last modification on : Friday, December 3, 2021 - 11:43:18 AM

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U1155 | SORBONNE-UNIVERSITE | SU-MEDECINE | SU-TI | INSERM

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Joëlle Nortier, Gauthier Remiche, Paul Delrée, Jeroen Nauta, Nicolette Notermans, et al.. Antenatal Membranous Nephropathy and Type 2 (Axonal) Charcot-Marie-Tooth With Mutations in the Metallo-Membrane Endopeptidase Gene: A Call for Family Screening and Pharmacovigilance. Kidney International Reports, Elsevier, 2021, 6 (7), pp.1981 - 1986. ⟨10.1016/j.ekir.2021.04.034⟩. ⟨hal-03333713⟩

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