Skip to content
DraconiticResearch
Search Sources API
201,818 studies31 sourcesUpdated 23 min ago
Peer-reviewedCC BY-NC-NDKidney international reports

Hypomagnesemia in Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome Caused by Pathogenic Variants of GATA3

  • Eveline J.E.M. Kahlman1
  • Nicole van der Zanden1
  • Ela Zaťková1
  • Caro Bos1
  • Justine Bacchetta2
  • Hendrica Belge3
  • Charlotte M.H.H.T. Bootsma-Robroeks4
  • Maria Luisa Brandi5
  • Jean-François Cambier6
  • Éloïse Colliou7
  • Nathalie Demoulin8
  • Lucile Figueres9
9 more authors
  • Laurence Heidet10
  • Giovanna Mantovani11
  • Matko Marlais12
  • John A. Sayer13
  • Karl P. Schlingmann14
  • Leo A. Monnens1
  • Joost G.J. Hoenderop1
  • Tom Nijenhuis15
  • Jeroen H.F. de Baaij1
15 affiliations
  1. 1Department of Medical BioSciences, Radboud University Medical Center, Nijmegen, The Netherlands
  2. 2LYOS INSERM1033 Research Unit, Department of Pediatric Nephrology, Rheumatology and Dermatology, Reference Center for Rare Renal Diseases, Reference Center for Rare Diseases of Phosphate and Calcium, Femme Mère Enfant Hospital, Hospices Civils de Lyon, Lyon, France
  3. 3Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium
  4. 4Department of Paediatrics, Paediatric Nephrology, Beatrix Children’s Hospital, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands
  5. 5Fondazione FIRMO Onlus (Italian Foundation for the Research on Bone Diseases), Florence, Italy
  6. 6Division of Nephrology, Grand hôpital de Charleroi, Gilly, Belgium
  7. 7Département de Néphrologie et Transplantation d’Organes, Centre de Référence des Maladies Rénales Rares, Centre Hospitalier Universitaire de Toulouse, Toulouse, France
  8. 8Division of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium
  9. 9Center for Research in Transplantation and Translational Immunology, INSERM, CHU Nantes, Nantes Université, UMR 1064, ITUN, Nantes, France
  10. 10Laboratoire des Maladies Rénales Héréditaires, Service de Néphrologie Pédiatrique Centre de Référence Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Hôpital Necker-Enfants Malades, Assistance Publique, Hôpitaux de Paris (AP-HP), Inserm UMR 1163, Institut Imagine, Université Paris Cité, Paris, France
  11. 11Endocrinology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy
  12. 12Department of Nephrology, Great Ormond Street Hospital for Children and UCL Great Ormond Street Institute of Child Health, London, UK
  13. 13NIHR Newcastle Biomedical Research Centre & Renal Services, Newcastle Hospitals NHS Foundation Trust, Biosciences Institute, Newcastle University, Newcastle upon Tyne, UK
  14. 14Department of General Pediatrics, Pediatric Nephrology, University Children’s Hospital, Münster, Germany
  15. 15Department of Nephrology, Radboud university medical center, Nijmegen, The Netherlands
Read full textPDFCite

Related

  1. Lorlatinib-associated sensorineural deafness in a non-small cell lung cancer patient with ALK-fusion: a Case Report
    Lijuan Cai, Wenying Peng, Runxiang Yang +3
    Frontiers in PharmacologyPeer-reviewedCC BY 4.0Pharmacology & toxicologyFrontiersCrossref
  2. Discontinuation of palopegteriparatide in chronic hypoparathyroidism without rebound hypocalcemia
    JCEM case reportsPeer-reviewedCC BY-NC-NDFull textEndocrinology & metabolismEurope PMC
  3. Contemporary and Emerging Therapeutic Strategies in Hypoparathyroidism: From Conventional Treatment to Restoration of Parathyroid Function
    Dominika Kochan-Olszewska, Aldona Kowalska
    Journal of clinical medicinePeer-reviewedCC BYFull textGeneral medicineEurope PMC
  4. Beyond Surgical Follow-Up: Measuring the Long-Term Burden of Permanent Hypoparathyroidism After Thyroid Cancer Surgery
    Rossella Melcarne, Jose Luis Carrillo Lizarazo, Marco Biffoni +4
    Medical sciences (Basel, Switzerland)Peer-reviewedCC BYFull textGeneral medicineEurope PMC
  5. Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis: A Case Report of Compound Heterozygous Variants in the CLDN16 Gene Inherited From Symptomatic Heterozygous Carriers
    Monica Ceol, Elena Sgrò, Franca Anglani +6
    Case Reports in Nephrology and DialysisPeer-reviewedCC BY 4.0Full textGeneral medicinePMC

Cite

BibTeXRIS
BibTeX
@article{kahlman2026hypomagnesemia,
  title = {{Hypomagnesemia in Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome Caused by Pathogenic Variants of GATA3}},
  author = {Eveline J.E.M. Kahlman and Nicole van der Zanden and Ela Zaťková and Caro Bos and Justine Bacchetta and Hendrica Belge and Charlotte M.H.H.T. Bootsma-Robroeks and Maria Luisa Brandi and Jean-François Cambier and Éloïse Colliou and Nathalie Demoulin and Lucile Figueres and Laurence Heidet and Giovanna Mantovani and Matko Marlais and John A. Sayer and Karl P. Schlingmann and Leo A. Monnens and Joost G.J. Hoenderop and Tom Nijenhuis and Jeroen H.F. de Baaij},
  journal = {Kidney international reports},
  year = {2026},
  month = sep,
  url = {https://europepmc.org/article/PMC/PMC13677023},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Hypomagnesemia in Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome Caused by Pathogenic Variants of GATA3
AU  - Eveline J.E.M. Kahlman
AU  - Nicole van der Zanden
AU  - Ela Zaťková
AU  - Caro Bos
AU  - Justine Bacchetta
AU  - Hendrica Belge
AU  - Charlotte M.H.H.T. Bootsma-Robroeks
AU  - Maria Luisa Brandi
AU  - Jean-François Cambier
AU  - Éloïse Colliou
AU  - Nathalie Demoulin
AU  - Lucile Figueres
AU  - Laurence Heidet
AU  - Giovanna Mantovani
AU  - Matko Marlais
AU  - John A. Sayer
AU  - Karl P. Schlingmann
AU  - Leo A. Monnens
AU  - Joost G.J. Hoenderop
AU  - Tom Nijenhuis
AU  - Jeroen H.F. de Baaij
PY  - 2026
DA  - 2026/09/16
JO  - Kidney international reports
UR  - https://europepmc.org/article/PMC/PMC13677023
SN  - 2468-0249
ER  -