Oro-Dental Features In Hypophosphatasia : A Valuable Phenotype For Disease Diagnosis And Evaluation Of Future Treatment Outcomes

Authors

  • A Bloch-Zupan Université de Strasbourg
  • Y Alembik Genetic Department and competence centre for diagnosis and management of osteochondrodysplasia
  • B Doray Genetic Department and competence centre for diagnosis and management of osteochondrodysplasia, HUS
  • A Linglart Hôpital Bicêtre Paris-Sud
  • E Mornet Université de Versailles
  • JJ Morrier Université de Lyon
  • D Droz Université de Nancy
  • MC Manière Université de Strasbourg

Abstract

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Author Biographies

A Bloch-Zupan, Université de Strasbourg

Faculty of Dentistry, Strasbourg; Reference Centre for Orodental Manifestations of rare diseases, HUS IGBMC, Illkirch

Y Alembik, Genetic Department and competence centre for diagnosis and management of osteochondrodysplasia

Genetic Department and competence centre for diagnosis and management of osteochondrodysplasia, HUS

B Doray, Genetic Department and competence centre for diagnosis and management of osteochondrodysplasia, HUS

Genetic Department and competence centre for diagnosis and management of osteochondrodysplasia, HUS

A Linglart, Hôpital Bicêtre Paris-Sud

Department of Paediatric Endocrinology and Reference Centre for phosphocalcic metabolism Hôpital Bicêtre Paris-Sud

E Mornet, Université de Versailles

IGBMC, Illkirch, France Unité de Génétique Constitutionnelle Prénatale et Postnatale, Service de Biologie, Centre Hospitalier de Versailles

JJ Morrier, Université de Lyon

Faculty of Dentistry Lyon

D Droz, Université de Nancy

Faculty of Dentistry, University of Nancy

MC Manière, Université de Strasbourg

Faculty of Dentistry, Strasbourg; Reference Centre for Orodental Manifestations of rare diseases, HUS

Published

2012-07-30