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Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)

Turner syndrome (TS; ORPHA 881) is a rare condition in which all or part of one X chromosome is absent from some or all cells. It affects approximately one in every 1/2500 liveborn girls. The most frequently observed karyotypes are 45,X (40–50%) and the 45,X/46,XX mosaic karyotype (15–25%). Karyotyp...

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Autores principales: Fiot, Elodie, Alauze, Bertille, Donadille, Bruno, Samara-Boustani, Dinane, Houang, Muriel, De Filippo, Gianpaolo, Bachelot, Anne, Delcour, Clemence, Beyler, Constance, Bois, Emilie, Bourrat, Emmanuelle, Bui Quoc, Emmanuel, Bourcigaux, Nathalie, Chaussain, Catherine, Cohen, Ariel, Cohen-Solal, Martine, Da Costa, Sabrina, Dossier, Claire, Ederhy, Stephane, Elmaleh, Monique, Iserin, Laurence, Lengliné, Hélène, Poujol-Robert, Armelle, Roulot, Dominique, Viala, Jerome, Albarel, Frederique, Bismuth, Elise, Bernard, Valérie, Bouvattier, Claire, Brac, Aude, Bretones, Patricia, Chabbert-Buffet, Nathalie, Chanson, Philippe, Coutant, Regis, de Warren, Marguerite, Demaret, Béatrice, Duranteau, Lise, Eustache, Florence, Gautheret, Lydie, Gelwane, Georges, Gourbesville, Claire, Grynberg, Mickaël, Gueniche, Karinne, Jorgensen, Carina, Kerlan, Veronique, Lebrun, Charlotte, Lefevre, Christine, Lorenzini, Françoise, Manouvrier, Sylvie, Pienkowski, Catherine, Reynaud, Rachel, Reznik, Yves, Siffroi, Jean-Pierre, Tabet, Anne-Claude, Tauber, Maithé, Vautier, Vanessa, Tauveron, Igor, Wambre, Sebastien, Zenaty, Delphine, Netchine, Irène, Polak, Michel, Touraine, Philippe, Carel, Jean-Claude, Christin-Maitre, Sophie, Léger, Juliane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277788/
https://www.ncbi.nlm.nih.gov/pubmed/35821070
http://dx.doi.org/10.1186/s13023-022-02423-5
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author Fiot, Elodie
Alauze, Bertille
Donadille, Bruno
Samara-Boustani, Dinane
Houang, Muriel
De Filippo, Gianpaolo
Bachelot, Anne
Delcour, Clemence
Beyler, Constance
Bois, Emilie
Bourrat, Emmanuelle
Bui Quoc, Emmanuel
Bourcigaux, Nathalie
Chaussain, Catherine
Cohen, Ariel
Cohen-Solal, Martine
Da Costa, Sabrina
Dossier, Claire
Ederhy, Stephane
Elmaleh, Monique
Iserin, Laurence
Lengliné, Hélène
Poujol-Robert, Armelle
Roulot, Dominique
Viala, Jerome
Albarel, Frederique
Bismuth, Elise
Bernard, Valérie
Bouvattier, Claire
Brac, Aude
Bretones, Patricia
Chabbert-Buffet, Nathalie
Chanson, Philippe
Coutant, Regis
de Warren, Marguerite
Demaret, Béatrice
Duranteau, Lise
Eustache, Florence
Gautheret, Lydie
Gelwane, Georges
Gourbesville, Claire
Grynberg, Mickaël
Gueniche, Karinne
Jorgensen, Carina
Kerlan, Veronique
Lebrun, Charlotte
Lefevre, Christine
Lorenzini, Françoise
Manouvrier, Sylvie
Pienkowski, Catherine
Reynaud, Rachel
Reznik, Yves
Siffroi, Jean-Pierre
Tabet, Anne-Claude
Tauber, Maithé
Vautier, Vanessa
Tauveron, Igor
Wambre, Sebastien
Zenaty, Delphine
Netchine, Irène
Polak, Michel
Touraine, Philippe
Carel, Jean-Claude
Christin-Maitre, Sophie
Léger, Juliane
author_facet Fiot, Elodie
Alauze, Bertille
Donadille, Bruno
Samara-Boustani, Dinane
Houang, Muriel
De Filippo, Gianpaolo
Bachelot, Anne
Delcour, Clemence
Beyler, Constance
Bois, Emilie
Bourrat, Emmanuelle
Bui Quoc, Emmanuel
Bourcigaux, Nathalie
Chaussain, Catherine
Cohen, Ariel
Cohen-Solal, Martine
Da Costa, Sabrina
Dossier, Claire
Ederhy, Stephane
Elmaleh, Monique
Iserin, Laurence
Lengliné, Hélène
Poujol-Robert, Armelle
Roulot, Dominique
Viala, Jerome
Albarel, Frederique
Bismuth, Elise
Bernard, Valérie
Bouvattier, Claire
Brac, Aude
Bretones, Patricia
Chabbert-Buffet, Nathalie
Chanson, Philippe
Coutant, Regis
de Warren, Marguerite
Demaret, Béatrice
Duranteau, Lise
Eustache, Florence
Gautheret, Lydie
Gelwane, Georges
Gourbesville, Claire
Grynberg, Mickaël
Gueniche, Karinne
Jorgensen, Carina
Kerlan, Veronique
Lebrun, Charlotte
Lefevre, Christine
Lorenzini, Françoise
Manouvrier, Sylvie
Pienkowski, Catherine
Reynaud, Rachel
Reznik, Yves
Siffroi, Jean-Pierre
Tabet, Anne-Claude
Tauber, Maithé
Vautier, Vanessa
Tauveron, Igor
Wambre, Sebastien
Zenaty, Delphine
Netchine, Irène
Polak, Michel
Touraine, Philippe
Carel, Jean-Claude
Christin-Maitre, Sophie
Léger, Juliane
author_sort Fiot, Elodie
collection PubMed
description Turner syndrome (TS; ORPHA 881) is a rare condition in which all or part of one X chromosome is absent from some or all cells. It affects approximately one in every 1/2500 liveborn girls. The most frequently observed karyotypes are 45,X (40–50%) and the 45,X/46,XX mosaic karyotype (15–25%). Karyotypes with an X isochromosome (45,X/46,isoXq or 45,X/46,isoXp), a Y chromosome, X ring chromosome or deletions of the X chromosome are less frequent. The objective of the French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins) is to provide health professionals with information about the optimal management and care for patients, based on a critical literature review and multidisciplinary expert consensus. The PNDS, written by members of the French National Reference Center for Rare Growth and Developmental Endocrine disorders, is available from the French Health Authority website. Turner Syndrome is associated with several phenotypic conditions and a higher risk of comorbidity. The most frequently reported features are growth retardation with short adult stature and gonadal dysgenesis. TS may be associated with various congenital (heart and kidney) or acquired diseases (autoimmune thyroid disease, celiac disease, hearing loss, overweight/obesity, glucose intolerance/type 2 diabetes, dyslipidemia, cardiovascular complications and liver dysfunction). Most of the clinical traits of TS are due to the haploinsufficiency of various genes on the X chromosome, particularly those in the pseudoautosomal regions (PAR 1 and PAR 2), which normally escape the physiological process of X inactivation, although other regions may also be implicated. The management of patients with TS requires collaboration between several healthcare providers. The attending physician, in collaboration 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 designed to provide such support.
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spelling pubmed-92777882022-07-14 Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol) Fiot, Elodie Alauze, Bertille Donadille, Bruno Samara-Boustani, Dinane Houang, Muriel De Filippo, Gianpaolo Bachelot, Anne Delcour, Clemence Beyler, Constance Bois, Emilie Bourrat, Emmanuelle Bui Quoc, Emmanuel Bourcigaux, Nathalie Chaussain, Catherine Cohen, Ariel Cohen-Solal, Martine Da Costa, Sabrina Dossier, Claire Ederhy, Stephane Elmaleh, Monique Iserin, Laurence Lengliné, Hélène Poujol-Robert, Armelle Roulot, Dominique Viala, Jerome Albarel, Frederique Bismuth, Elise Bernard, Valérie Bouvattier, Claire Brac, Aude Bretones, Patricia Chabbert-Buffet, Nathalie Chanson, Philippe Coutant, Regis de Warren, Marguerite Demaret, Béatrice Duranteau, Lise Eustache, Florence Gautheret, Lydie Gelwane, Georges Gourbesville, Claire Grynberg, Mickaël Gueniche, Karinne Jorgensen, Carina Kerlan, Veronique Lebrun, Charlotte Lefevre, Christine Lorenzini, Françoise Manouvrier, Sylvie Pienkowski, Catherine Reynaud, Rachel Reznik, Yves Siffroi, Jean-Pierre Tabet, Anne-Claude Tauber, Maithé Vautier, Vanessa Tauveron, Igor Wambre, Sebastien Zenaty, Delphine Netchine, Irène Polak, Michel Touraine, Philippe Carel, Jean-Claude Christin-Maitre, Sophie Léger, Juliane Orphanet J Rare Dis Position Statement Turner syndrome (TS; ORPHA 881) is a rare condition in which all or part of one X chromosome is absent from some or all cells. It affects approximately one in every 1/2500 liveborn girls. The most frequently observed karyotypes are 45,X (40–50%) and the 45,X/46,XX mosaic karyotype (15–25%). Karyotypes with an X isochromosome (45,X/46,isoXq or 45,X/46,isoXp), a Y chromosome, X ring chromosome or deletions of the X chromosome are less frequent. The objective of the French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins) is to provide health professionals with information about the optimal management and care for patients, based on a critical literature review and multidisciplinary expert consensus. The PNDS, written by members of the French National Reference Center for Rare Growth and Developmental Endocrine disorders, is available from the French Health Authority website. Turner Syndrome is associated with several phenotypic conditions and a higher risk of comorbidity. The most frequently reported features are growth retardation with short adult stature and gonadal dysgenesis. TS may be associated with various congenital (heart and kidney) or acquired diseases (autoimmune thyroid disease, celiac disease, hearing loss, overweight/obesity, glucose intolerance/type 2 diabetes, dyslipidemia, cardiovascular complications and liver dysfunction). Most of the clinical traits of TS are due to the haploinsufficiency of various genes on the X chromosome, particularly those in the pseudoautosomal regions (PAR 1 and PAR 2), which normally escape the physiological process of X inactivation, although other regions may also be implicated. The management of patients with TS requires collaboration between several healthcare providers. The attending physician, in collaboration 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 designed to provide such support. BioMed Central 2022-07-12 /pmc/articles/PMC9277788/ /pubmed/35821070 http://dx.doi.org/10.1186/s13023-022-02423-5 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
Fiot, Elodie
Alauze, Bertille
Donadille, Bruno
Samara-Boustani, Dinane
Houang, Muriel
De Filippo, Gianpaolo
Bachelot, Anne
Delcour, Clemence
Beyler, Constance
Bois, Emilie
Bourrat, Emmanuelle
Bui Quoc, Emmanuel
Bourcigaux, Nathalie
Chaussain, Catherine
Cohen, Ariel
Cohen-Solal, Martine
Da Costa, Sabrina
Dossier, Claire
Ederhy, Stephane
Elmaleh, Monique
Iserin, Laurence
Lengliné, Hélène
Poujol-Robert, Armelle
Roulot, Dominique
Viala, Jerome
Albarel, Frederique
Bismuth, Elise
Bernard, Valérie
Bouvattier, Claire
Brac, Aude
Bretones, Patricia
Chabbert-Buffet, Nathalie
Chanson, Philippe
Coutant, Regis
de Warren, Marguerite
Demaret, Béatrice
Duranteau, Lise
Eustache, Florence
Gautheret, Lydie
Gelwane, Georges
Gourbesville, Claire
Grynberg, Mickaël
Gueniche, Karinne
Jorgensen, Carina
Kerlan, Veronique
Lebrun, Charlotte
Lefevre, Christine
Lorenzini, Françoise
Manouvrier, Sylvie
Pienkowski, Catherine
Reynaud, Rachel
Reznik, Yves
Siffroi, Jean-Pierre
Tabet, Anne-Claude
Tauber, Maithé
Vautier, Vanessa
Tauveron, Igor
Wambre, Sebastien
Zenaty, Delphine
Netchine, Irène
Polak, Michel
Touraine, Philippe
Carel, Jean-Claude
Christin-Maitre, Sophie
Léger, Juliane
Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)
title Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)
title_full Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)
title_fullStr Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)
title_full_unstemmed Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)
title_short Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)
title_sort turner syndrome: french national diagnosis and care protocol (ndcp; national diagnosis and care protocol)
topic Position Statement
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277788/
https://www.ncbi.nlm.nih.gov/pubmed/35821070
http://dx.doi.org/10.1186/s13023-022-02423-5
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