Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop’s classification

Autor: Agnes Bloch-Zupan, Tristan Rey, Alexandra Jimenez-Armijo, Marzena Kawczynski, Naji Kharouf, O-Rare consortium, Muriel de La Dure-Molla, Emmanuelle Noirrit, Magali Hernandez, Clara Joseph-Beaudin, Serena Lopez, Corinne Tardieu, Béatrice Thivichon-Prince, ERN Cranio Consortium, Tatjana Dostalova, Milan Macek, International Consortium, Mustapha El Alloussi, Leila Qebibo, Supawich Morkmued, Patimaporn Pungchanchaikul, Blanca Urzúa Orellana, Marie-Cécile Manière, Bénédicte Gérard, Isaac Maximiliano Bugueno, Virginie Laugel-Haushalter, Yves Alembik, Victorin Ahossi, Isabelle Bailleul-Forestier, Isabelle Blanchet, Ariane Berdal, Marie José Boileau, Nicolas Chassaing, François Clauss, Caroline Delfosse, Anne De-Saint-Martin, Jean-Christophe Dahlet, Bérénice Doray, Jean-Luc Davideau, Tiphaine Davit-Béal, Hélène Dollfus, Jean-Pierre Duprez, Muriel de La Dure Molla, Klauss Dieterich, Dominique Droz, Salima El Chehadeh, Olivier Etienne, Edouard Euvrard, Laurence Faivre, Benjamin Fournier, Elsa Garot, Bruno Grollemund, Nathalie Guffon-Fouilhoux, Mathilde Huckert, Bertand Isidor, Sophie Jung, Didier Lacombe, Alinoe Lavillaurex, Marine Lebrun, Bruno Leheup, Adeline Loing, Sandrine Marlin, Jean-Jacques Morrier, Michèle Muller-Bolla, Sylvie Odent, Marie Paule Gelle, Juliette Piard, Linda Pons, Béatrice Richard, Massimiliano Rossi, Prune Sadones, Elise Schaefer, Jean-Louis Sixou, Sylvie Soskin, Marion Strub, Annick Toutain, Alain Verloes, Frédéric Vaysse, Delphine Wagner

Publikováno v: Frontiers in Physiology, Vol 14 (2023)

Amelogenesis imperfecta (AI) is a heterogeneous group of genetic rare diseases disrupting enamel development (Smith et al., Front Physiol, 2017a, 8, 333). The clinical enamel phenotypes can be described as hypoplastic, hypomineralized or hypomature a

Externí odkaz: https://doaj.org/article/be19745ebc994351a79834498f898534

Best clinical practice guidance for clinicians dealing with children presenting with molar-incisor-hypomineralisation (MIH): an updated European Academy of Paediatric Dentistry policy document

Autor: C Somani, GD Taylor, Elsa Garot, N A Lygidakis, Patrick Rouas, Ferranti S. L. Wong

Publikováno v: European Archives of Paediatric Dentistry. 23:3-21

Aim To update the existing European Academy of Paediatric Dentistry (EAPD) 2010 policy document on the ‘Best Clinical Practice guidance for clinicians dealing with children presenting with Molar-Incisor-Hypomineralisation (MIH).’ Methods Experts,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::293866d8b77974acdcc5b05b3853d818
https://doi.org/10.1007/s40368-021-00668-5

The prevalence, characteristics and association between MIH and HSPM in South-Western France

Autor: Julia, Estivals, Caroline, Fahd, Jeanne, Baillet, Patrick, Rouas, David John, Manton, Elsa, Garot

Publikováno v: International journal of paediatric dentistry.

Molar-Incisor Hypomineralisation (MIH) and Hypomineralised Second Primary Molars (HSPM) involve qualitative structural developmental anomalies of tooth enamel affecting the first permanent molars and the second primary molars, respectively. This deve

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::eb7a7089d446abd31a4db15ff980405a
https://pubmed.ncbi.nlm.nih.gov/36511101

An update of the aetiological factors involved in molar incisor hypomineralisation (MIH): a systematic review and meta-analysis

Autor: GD Taylor, Elsa Garot, C Somani, N A Lygidakis, Ferranti S. L. Wong, Patrick Rouas

Publikováno v: European Archives of Paediatric Dentistry. 23:23-38

To systematically review the aetiological factors associated with molar incisor hypomineralisation (MIH). To this day, the aetiology remains unknown. Determining risk factors would allow risk assessment and enhance early diagnosis of MIH in young pat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f88d71154e93df2576e8bc0eab7a7662
https://doi.org/10.1007/s40368-021-00646-x

Knowledge and Management of First Permanent Molars with Enamel Hypomineralization among Dentists and Orthodontists

Autor: M J Boileau, David J. Manton, T Carat, Elsa Garot, J Craveia, Patrick Rouas

Publikováno v: The Journal of clinical pediatric dentistry, 44(1), 20-27

Purpose: Molar Incisor Hypomineralization (MIH) is a developmental enamel anomaly of systemic origin affecting the first permanent molars and often the permanent incisors. Despite MIH being a prevalent anomaly, its diagnosis and management are challe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e100f6b925a61f6f17976e0ea670ab8
https://doi.org/10.17796/1053-4625-44.1.4