Cancer surveillance in children with Ollier Disease and Maffucci Syndrome

Am J Med Genet A. 2021 Apr;185(4):1338-1340. doi: 10.1002/ajmg.a.62078. Epub 2021 Jan 12.

Authors

Manuel Diezi¹, Pierre-Yves Zambelli², Andrea Superti-Furga³, Sheila Unger³, Raffaele Renella¹

Affiliations

¹ Pediatric Hematology-Oncology Unit, Division of Pediatrics, Department "Woman-Mother-Child", Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
² Division of Pediatric Surgery, Lausanne University Hospital, Lausanne, Switzerland.
³ Division of Genetic Medicine, Department of Medicine, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

PMID: 33433055
DOI: 10.1002/ajmg.a.62078

No abstract available

Publication types

Letter

MeSH terms

Adult
Bone Neoplasms / complications
Bone Neoplasms / epidemiology*
Bone Neoplasms / genetics
Bone Neoplasms / pathology
Enchondromatosis / complications
Enchondromatosis / epidemiology*
Enchondromatosis / genetics*
Enchondromatosis / pathology
Female
Genetic Predisposition to Disease
Humans
Isocitrate Dehydrogenase / genetics*
Male

Substances

Isocitrate Dehydrogenase
IDH1 protein, human