Microcomputed tomography and genetic analysis of a rare case of Caffey's disease in a 5–7‐month‐old girl-Reference-Cited by-同舟云学术

Microcomputed tomography and genetic analysis of a rare case of Caffey's disease in a 5–7‐month‐old girl

Published:2019-07-17 Issue:5 Volume:29 Page:854-859
ISSN:1047-482X
Container-title:International Journal of Osteoarchaeology
language:en
Short-container-title:Int J Osteoarchaeol

Author:

Lombardo Daniela¹^ORCID,Modi Alessandra²,Vergata Chiara²,Caramelli David²,Pascart Tristan³,Bertrand Benoit¹,Vetro Annalisa⁴,Lari Martina²,Colard Thomas¹⁵

Affiliation:

1. CHRU LilleUniversité de Lille Lille France

2. Laboratory of Anthropology, Department of BiologyUniversity of Florence Florence Italy

3. Rheumatology departmentLille Catholic Hospital, and University of Lille 2 Lille France

4. Pediatric Neurology, Neurogenetics and Neurobiology Unit and LaboratoriesMeyer Children's Hospital, University of Florence Florence Italy

5. UMR 5199 PACEA, CNRS, MCCUniversity of Bordeaux, LabEx Sciences archéologiques de Bordeaux Pessac France

Publisher

Wiley

Subject

Archeology,Anthropology,Archeology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/oa.2772

Reference28 articles.

1. Brief communication: The London atlas of human tooth development and eruption

2. Infantile cortical hyperostosis, preliminary report of a new syndrome;Caffey J.;American Journal of Rontgenology,1945

3. Infantile cortical hyperostosis and COL1A1 mutation in four generations

4. The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease)

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