Ollier disease and Maffucci syndrome are the commonest enchondromatosis subtypes,
arising from non-hereditary mutations in the IDH1 and IDH2 genes, presenting in childhood …

Introduction This review was done to find the trend for orthopaedic publications from Egypt in
the last 5 years, detailing the specialties that are most published and comparing this with the …

Background Maffucci's syndrome is characterized by the coexistence of multiple
enchondromas and soft-tissue hemangiomas. It has been clear that somatic mosaic …

The anatomical collection of the Anatomical Museum of Leiden University Medical Center
(historically referred to as Museum Anatomicum Academiae Lugduno‐Batavae) houses and …

Background: Multiple enchondromas in the pediatric hand is a relatively rare occurrence
and the literature regarding its incidence and treatment is sparse. Within this rare subset of …

Ollier disease is a rare skeletal dysplasia characterized by the formation of multiple
enchondromas (enchondromatosis), typically in the long bones of the extremities. These …

Trotz des häufigen Auftretens von Enchondromen an der Hand gibt es momentan keinen
therapeutischen Standard. Das Ziel der Studie bestand darin, demographische Faktoren …

Introduction Most tumour-related pathological fractures occur in patients with bone
metastases. However, in mostly younger patients, a pathological fracture can be due to both …

лЕчЕНиЕ ПациЕНТа С БОлЕзНью ОльЕ TrEaTMENT OF a PaTiENT wiTh OlliEr’S
DiSEaSE Page 1 73 Наблюдения из практики / Observation from practice УчЁные …

Le sindromi encondromatosiche, in particolare la sindrome di Ollier e la sindrome di
Maffucci, sono patologie rare che dimostrano di frequente un coinvolgimento dei segmenti …