📇 Rhumatologue · LIVAROT PAYS D AUGE · (14) · Salarié
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3 raisons identifiées
Référence presse grand public
Cité 2 fois dans les médias — pédagogie reconnue
Disponibilité géographique
2 lieux d'exercice — choisissez celui qui vous arrange
Délais de RDV courts dans la région
150.8 rhumatos / 100 000 hab. — département bien doté
✨ Génération du profil synthétique IA en cours…
EHPAD SAINT JOSEPH - LIVAROT
55 R GENERAL LECLERC, 14140 LIVAROT PAYS D AUGE
Secteur de conventionnement non disponible (médecin hospitalier ou non présent dans l'Annuaire santé CNAM des libéraux conventionnés).
Données ANS publiques (Licence Ouverte 2.0) · Enrichissements MonRhumato 100 % opt-in · Toute personne référencée peut demander la suppression ou la rectification.
Lien Doctolib = recherche Google site:doctolib.fr (le 1er résultat est presque toujours le profil correct s'il existe).
Source : Google News (recherche par nom complet — homonymes possibles, vérifier le contenu).
📰 Actu.fr · 21/03/2025
<a href="https://news.google.com/rss/articles/CBMiwwFBVV95cUxNN21LaU9mNnlqaUFXUVBKVTBmd3dZeVRjd0gxdGxoR1otdWFHM0d6b3E1Q3V2Z1V1NWpZbUdYY1k5SmJJMlJVdVJ5aHpTM3cyQWpHUWNzdmxfMTVQek1wajV4cFdLLWhwazduSVJqWGpaNmNsUUhmNkJNRG1YQWxrM2IyaUJ2Y2J5eUlOS2tCZ0RPTTlCVE44dkpFMGtwMTVLX0FSbXpwcFBqQTA4NFUxUDgzbUswcEhTeG
📰 Ouest-France · 17/02/2018
<a href="https://news.google.com/rss/articles/CBMivgFBVV95cUxOMmJPYUR4TjBneVZyeFVWd0FsbnhaS3otazgtdjlqbUs2RU0xSmxSajhWRHpSYXBURVdNSnBRN0h5WjRnR1dmNnRadXl0bEIxY01UUWtmeWRsZFpKLUdEdU9IV1VJbUpCMDMxaDNiZHAwRnpZc1BvWTFjcmlSNnhVRm9YVl9lakp0NjJxeGZqV1FNVGs0R1NobU9OVC1vU1UxSHJmMHpzQUZfRDhXajhCSXJRT0tLNUdBVX
Orphanet journal of rare diseases · 2022
AbstractTurner 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.
Frontiers in human neuroscience · 2012
Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).
Orphanet journal of rare diseases · 2022 · Journal Article
Fiot E, Alauze B, Donadille B, Samara-Boustani D, et al.
Frontiers in human neuroscience · 2012 · Journal Article
Bejanin A, Viard A, Chételat G, Clarys D, et al.