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Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)

Dunnigan syndrome, or Familial Partial Lipodystrophy type 2 (FPLD2; ORPHA 2348), is a rare autosomal dominant disorder due to pathogenic variants of the LMNA gene. The objective of the French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins), is to provide hea...

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Autores principales: Mosbah, H., Donadille, B., Vatier, C., Janmaat, S., Atlan, M., Badens, C., Barat, P., Béliard, S., Beltrand, J., Ben Yaou, R., Bismuth, E., Boccara, F., Cariou, B., Chaouat, M., Charriot, G., Christin-Maitre, S., De Kerdanet, M., Delemer, B., Disse, E., Dubois, N., Eymard, B., Fève, B., Lascols, O., Mathurin, P., Nobécourt, E., Poujol-Robert, A., Prevost, G., Richard, P., Sellam, J., Tauveron, I., Treboz, D., Vergès, B., Vermot-Desroches, V., Wahbi, K., Jéru, I., Vantyghem, M. C., Vigouroux, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019936/
https://www.ncbi.nlm.nih.gov/pubmed/35440056
http://dx.doi.org/10.1186/s13023-022-02308-7
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author Mosbah, H.
Donadille, B.
Vatier, C.
Janmaat, S.
Atlan, M.
Badens, C.
Barat, P.
Béliard, S.
Beltrand, J.
Ben Yaou, R.
Bismuth, E.
Boccara, F.
Cariou, B.
Chaouat, M.
Charriot, G.
Christin-Maitre, S.
De Kerdanet, M.
Delemer, B.
Disse, E.
Dubois, N.
Eymard, B.
Fève, B.
Lascols, O.
Mathurin, P.
Nobécourt, E.
Poujol-Robert, A.
Prevost, G.
Richard, P.
Sellam, J.
Tauveron, I.
Treboz, D.
Vergès, B.
Vermot-Desroches, V.
Wahbi, K.
Jéru, I.
Vantyghem, M. C.
Vigouroux, C.
author_facet Mosbah, H.
Donadille, B.
Vatier, C.
Janmaat, S.
Atlan, M.
Badens, C.
Barat, P.
Béliard, S.
Beltrand, J.
Ben Yaou, R.
Bismuth, E.
Boccara, F.
Cariou, B.
Chaouat, M.
Charriot, G.
Christin-Maitre, S.
De Kerdanet, M.
Delemer, B.
Disse, E.
Dubois, N.
Eymard, B.
Fève, B.
Lascols, O.
Mathurin, P.
Nobécourt, E.
Poujol-Robert, A.
Prevost, G.
Richard, P.
Sellam, J.
Tauveron, I.
Treboz, D.
Vergès, B.
Vermot-Desroches, V.
Wahbi, K.
Jéru, I.
Vantyghem, M. C.
Vigouroux, C.
author_sort Mosbah, H.
collection PubMed
description Dunnigan syndrome, or Familial Partial Lipodystrophy type 2 (FPLD2; ORPHA 2348), is a rare autosomal dominant disorder due to pathogenic variants of the LMNA gene. The objective of the French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins), is to provide health professionals with a guide to optimal management and care of patients with FPLD2, based on a critical literature review and multidisciplinary expert consensus. The PNDS, written by members of the French National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), is available on the French Health Authority website (in French). Dunnigan syndrome is characterized by a partial atrophy of the subcutaneous adipose tissue and by an insulin resistance syndrome, associated with a risk of metabolic, cardiovascular and muscular complications. Its prevalence, assessed at 1/100.000 in Europe, is probably considerably underestimated. Thorough clinical examination is key to diagnosis. Biochemical testing frequently shows hyperinsulinemia, abnormal glucose tolerance and hypertriglyceridemia. Elevated hepatic transaminases (hepatic steatosis) and creatine phosphokinase, and hyperandrogenism in women, are common. Molecular analysis of the LMNA gene confirms diagnosis and allows for family investigations. Regular screening and multidisciplinary monitoring of the associated complications are necessary. Diabetes frequently develops from puberty onwards. Hypertriglyceridemia may lead to acute pancreatitis. Early atherosclerosis and cardiomyopathy should be monitored. In women, polycystic ovary syndrome is common. Overall, the management of patients with Dunnigan syndrome requires the collaboration of several health care providers. The attending physician, in conjunction with the national care network, will ensure that the patient receives optimal care through regular follow-up and screening. The various elements of this PNDS are described to provide such a support.
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spelling pubmed-90199362022-04-21 Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins) Mosbah, H. Donadille, B. Vatier, C. Janmaat, S. Atlan, M. Badens, C. Barat, P. Béliard, S. Beltrand, J. Ben Yaou, R. Bismuth, E. Boccara, F. Cariou, B. Chaouat, M. Charriot, G. Christin-Maitre, S. De Kerdanet, M. Delemer, B. Disse, E. Dubois, N. Eymard, B. Fève, B. Lascols, O. Mathurin, P. Nobécourt, E. Poujol-Robert, A. Prevost, G. Richard, P. Sellam, J. Tauveron, I. Treboz, D. Vergès, B. Vermot-Desroches, V. Wahbi, K. Jéru, I. Vantyghem, M. C. Vigouroux, C. Orphanet J Rare Dis Position Statement Dunnigan syndrome, or Familial Partial Lipodystrophy type 2 (FPLD2; ORPHA 2348), is a rare autosomal dominant disorder due to pathogenic variants of the LMNA gene. The objective of the French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins), is to provide health professionals with a guide to optimal management and care of patients with FPLD2, based on a critical literature review and multidisciplinary expert consensus. The PNDS, written by members of the French National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), is available on the French Health Authority website (in French). Dunnigan syndrome is characterized by a partial atrophy of the subcutaneous adipose tissue and by an insulin resistance syndrome, associated with a risk of metabolic, cardiovascular and muscular complications. Its prevalence, assessed at 1/100.000 in Europe, is probably considerably underestimated. Thorough clinical examination is key to diagnosis. Biochemical testing frequently shows hyperinsulinemia, abnormal glucose tolerance and hypertriglyceridemia. Elevated hepatic transaminases (hepatic steatosis) and creatine phosphokinase, and hyperandrogenism in women, are common. Molecular analysis of the LMNA gene confirms diagnosis and allows for family investigations. Regular screening and multidisciplinary monitoring of the associated complications are necessary. Diabetes frequently develops from puberty onwards. Hypertriglyceridemia may lead to acute pancreatitis. Early atherosclerosis and cardiomyopathy should be monitored. In women, polycystic ovary syndrome is common. Overall, the management of patients with Dunnigan syndrome requires the collaboration of several health care providers. The attending physician, in conjunction with the national care network, will ensure that the patient receives optimal care through regular follow-up and screening. The various elements of this PNDS are described to provide such a support. BioMed Central 2022-04-19 /pmc/articles/PMC9019936/ /pubmed/35440056 http://dx.doi.org/10.1186/s13023-022-02308-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Position Statement
Mosbah, H.
Donadille, B.
Vatier, C.
Janmaat, S.
Atlan, M.
Badens, C.
Barat, P.
Béliard, S.
Beltrand, J.
Ben Yaou, R.
Bismuth, E.
Boccara, F.
Cariou, B.
Chaouat, M.
Charriot, G.
Christin-Maitre, S.
De Kerdanet, M.
Delemer, B.
Disse, E.
Dubois, N.
Eymard, B.
Fève, B.
Lascols, O.
Mathurin, P.
Nobécourt, E.
Poujol-Robert, A.
Prevost, G.
Richard, P.
Sellam, J.
Tauveron, I.
Treboz, D.
Vergès, B.
Vermot-Desroches, V.
Wahbi, K.
Jéru, I.
Vantyghem, M. C.
Vigouroux, C.
Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)
title Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)
title_full Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)
title_fullStr Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)
title_full_unstemmed Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)
title_short Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)
title_sort dunnigan lipodystrophy syndrome: french national diagnosis and care protocol (pnds; protocole national de diagnostic et de soins)
topic Position Statement
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019936/
https://www.ncbi.nlm.nih.gov/pubmed/35440056
http://dx.doi.org/10.1186/s13023-022-02308-7
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