Muriel de la DURE-MOLLA

PU-PH - Service d’Odontologie Hôpital Rothschild - APHP

WP1

RÉSEAU DDS CENTRÉ SUR LE PATIENT

Centre de Référence des Maladies Rares Orales et Dentaires. Paris-Rothschild

Pôles d’activités

Coordination du Centre de Référence des Maladies Rares Orales et Dentaires oRares
Prise en charge diagnostique et thérapeutique des Maladies Rares Orales et Dentaires chez l’enfant et l’adulte
Etablissement de guides de bonnes pratiques, consensus, PNDS
Pilotage de réseaux d’expertise
Référent auprès des autres filière et CRMR
Connexion avec les associations de malades, le réseau ORARES, la filière TETECOU et les réseaux européen

Projets

Corrélation génotype / phénotype de différentes pathologies (agénésies dentaires, incontinentia pigmenti, amélogenèse imparfaites, dentinogenèse imparfaites)
Caractérisation des anomalies de l’os cranio-facial chez les patients atteints d’ostéogenèse imparfaite
Caractérisation du phénotype dentaire de diverses maladies rares (syndrome de Gardner, dysplasie ostéoglophonique …)

Publications récentes

Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogenesis Imperfecta . J Dent Res. 2023 Mar 23. doi: 10.1177/00220345231154569. PMID: 36951356
The dental triage method at Rothschild Hospital during the first lockdown due to the COVID-19 pandemic. PLoS One. 2023 Feb. doi: 10.1371/journal.pone.0281390.
Oral Phenotype of Singleton-Merten Syndrome: A Systematic Review Illustrated With a Case Report. Front Genet. 2022. PMID: 35754802
International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia. Nat Rev Endocrinol. 2022 Mar. PMID: 34837063
Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti. JEADV 2020, doi: 10.1111/jdv.16403.
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders. Am J Med Genet A. 2019. doi: 10.1002/ajmg.a.61316
Oral health related quality of life of children and adolescents affected by rare orofacial diseases: a questionnaire-based cohort study. MD. Orphanet J Rare Dis. 2019. PMID: 31164137
Management of rare diseases of the Head, Neck and Teeth: results of a French population-based prospective 8-year study. Orphanet J Rare Dis. 2017. PMID: 28526043
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations. J Med Genet 2017. PMID: 27530400

Actualités

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