Maturity Onset Diabetes of the Young (MODY): French National Diagnosis and Care Protocol (PNDS, Protocole National de Diagnostic et de Soins).

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Title: Maturity Onset Diabetes of the Young (MODY): French National Diagnosis and Care Protocol (PNDS, Protocole National de Diagnostic et de Soins).
Authors: Dubois-Laforgue D; Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Department of Diabetology and Clinical Immunology, Paris-Cité University & INSERM U1016, Cochin Institute, Paris, France., Donadille B; Assistance Publique-Hôpitaux de Paris, Saint-Antoine Hospital, National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Endocrinology, Diabetology and Reproductive Endocrinology Department, Sorbonne University, European Reference Network for Rare Endocrine Conditions (Endo-ERN Assistance-Publique Consortium), Paris, France. bruno.donadille@aphp.fr., Ciangura C; Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Diabetology Department, Sorbonne University, Paris, France., Amouyal C; Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Diabetology Department, Sorbonne University, Paris, France., Arnoux JB; Assistance Publique-Hôpitaux de Paris, Necker-Enfants Maladies Hospital, Reference Center for Inherited Metabolic Diseases, Paris-Cité University, G2M Network, Imagine Institute, Paris, France., Barat P; Univ. Bordeaux, CHU Bordeaux, Paediatric Endocrinology and Diabetology Department, Bordeaux, France., Baron S; Nantes University, University Hospital, Paediatric Endocrinology Department, Nantes, France., Beltrand J; Assistance Publique-Hôpitaux de Paris, Necker Enfants Malades Hospital, Paediatric Endocrinology, Gynecology and Diabetology Department, Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS); European Reference Network for Rare Endocrine Conditions (Endo-ERN Assistance-Publique Consortium) Paris-Cité University & INSERM U106 Cochin Institute and U1163 Imagine Institute, Paris, France., Bismuth E; Assistance Publique-Hôpitaux de Paris, Robert Debré Hospital, Pediatric Endocrinology and Diabetes Department, Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Paris-Cité University, Paris, France., Bouché C; Rothschild Foundation, Diabetology Department, Paris, France., Carel JC; Assistance Publique-Hôpitaux de Paris, Robert Debré Hospital, Pediatric Endocrinology and Diabetes Department, Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Paris-Cité University, Paris, France., Cavé H; Assistance Publique-Hôpitaux de Paris, Robert Debré Hospital, Molecular Genetics Department, Paris-Cité University, Paris, France., Christin-Maitre S; Assistance Publique-Hôpitaux de Paris, Saint-Antoine Hospital, National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Endocrinology, Diabetology and Reproductive Endocrinology Department, Sorbonne University, European Reference Network for Rare Endocrine Conditions (Endo-ERN Assistance-Publique Consortium), Paris, France.; Sorbonne University, Inserm UMR_S933, Paris, France., Collin-Chavagnac D; Hospices Civils de Lyon HCL, Biochemistry and Molecular Biology Department, Lyon, and CarMeN Laboratory, Claude Bernard Lyon 1 University, Inserm, INRAE, Pierre-Bénite, France., Damgé C; Patient Association Fédération Française des Diabétiques, Paris, France., Delemer B; Reims University, Reims University Hospital, Endocrinology-Diabetology Department, Reims, France., Gourdy P; Toulouse University, Toulouse University Hospital, Endocrinology-Diabetology-Nutrition Department and INSERM, I2MC UMR1297, Toulouse, France., Jacqueminet S; Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Diabetology Department, Sorbonne University, Paris, France., Janmaat S; Assistance Publique-Hôpitaux de Paris, Saint-Antoine Hospital, National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Endocrinology, Diabetology and Reproductive Endocrinology Department, Sorbonne University, European Reference Network for Rare Endocrine Conditions (Endo-ERN Assistance-Publique Consortium), Paris, France.; Sorbonne University, Inserm UMR_S938, Saint-Antoine Research Centre, Institute of Cardiometabolism and Nutrition, Paris, France., de Kerdanet M; Rennes University Hospitals, South Hospital, Paediatric Endocrinology Department, Rennes, France.; Patient Association Aide aux Jeunes Diabétiques, Paris, France., Kessler L; Strasbourg University, Strasbourg Civil Hospital, Endocrinology-Diabetology Department, Strasbourg, France., Langin D; Toulouse University, Toulouse University Hospital, Genetics Department, Toulouse, France., Nault JC; Assistance Publique-Hôpitaux de Paris, Avicenne Hospital, Hepatology Department, Paris 13 University, Bobigny, France., Nizard J; Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Obstetrics Department, Sorbonne University, Paris, France., Polak M; Assistance Publique-Hôpitaux de Paris, Necker Enfants Malades Hospital, Paediatric Endocrinology, Gynecology and Diabetology Department, Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS); European Reference Network for Rare Endocrine Conditions (Endo-ERN Assistance-Publique Consortium) Paris-Cité University & INSERM U106 Cochin Institute and U1163 Imagine Institute, Paris, France.; Paris city University, INSERM units U1016 (Cochin institute) and U1163 (Imagine institute), Paris, France., Reynaud R; Assistance Publique-Hôpitaux de Marseille, Timone Children Hospital, Pediatric multidisciplinary department, Marseille, France., Saint-Martin C; Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Medical Genetics Department, Sorbonne University, Paris, France., Tauveron I; Clermont-Ferrand University Hospital, Endocrinology Department, Clermont Auvergne University, Clermont-Ferrand, France., Valéro R; Aix Marseille University, Assistance Publique Hôpitaux de Marseille, INSERM-INRAE-C2VN, University Hospital La Conception, Department of Nutrition, Metabolic Diseases and Endocrinology, Marseille, France., Vambergue A; Lille University, Claude-Huriez University Hospital, Department of Diabetes and Nutrition, EGID Center, Lille, France., Vantyghem MC; University Hospital of Lille, Department of Diabetes and Nutrition, EGID Center, University of Lille, Lille, France., Vatier C; Assistance Publique-Hôpitaux de Paris, Saint-Antoine Hospital, National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Endocrinology, Diabetology and Reproductive Endocrinology Department, Sorbonne University, European Reference Network for Rare Endocrine Conditions (Endo-ERN Assistance-Publique Consortium), Paris, France.; Sorbonne University, Inserm UMR_S938, Saint-Antoine Research Centre, Institute of Cardiometabolism and Nutrition, Paris, France., Nicolino M; Lyon University, CHU de Lyon HCL-GH Est, Mère Enfant Hospital, Endocrinology Department, Lyon, France., Bellanné-Chantelot C; Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Medical Genetics Department, Sorbonne University, Paris, France., Vigouroux C; Assistance Publique-Hôpitaux de Paris, Saint-Antoine Hospital, National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Endocrinology, Diabetology and Reproductive Endocrinology Department, Sorbonne University, European Reference Network for Rare Endocrine Conditions (Endo-ERN Assistance-Publique Consortium), Paris, France.; Sorbonne University, Inserm UMR_S938, Saint-Antoine Research Centre, Institute of Cardiometabolism and Nutrition, Paris, France.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2026 Mar 31; Vol. 17 (Suppl 1). Date of Electronic Publication: 2026 Mar 31.
Publication Type: Journal Article; Review
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1750-1172
DOI:10.1186/s13023-026-04272-y