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J Pediatr Orthop ; 20(2): 246-50, 2000.
Article in English | MEDLINE | ID: mdl-10739291

ABSTRACT

Hereditary multiple exostoses (HME) is traditionally described as a skeletal dysplasia. However, the discovery that the EXT family of tumour suppressor genes are responsible for HME suggests that it is more appropriate to classify HME as a familial neoplastic trait. In a clinical and radiographic analysis of paired bone length and exostoses number and dimensions in a HME cohort, the local presence of osteochondromas was consistently associated with growth disturbance. In particular, an inverse correlation between osteochondroma size and relative bone length (p<0.01) was found. These data suggest that the growth retardation in HME may result from the local effects of enlarging osteochondromas rather than a skeletal dysplasia effect. This study provides the first clinical rationale for ablation of rapidly enlarging exostoses to reduce growth disturbance.


Subject(s)
Bone Neoplasms/diagnostic imaging , Exostoses, Multiple Hereditary/diagnosis , Growth Disorders/diagnostic imaging , Osteochondroma/diagnostic imaging , Osteochondroma/pathology , Adolescent , Adult , Bone Neoplasms/genetics , Bone Neoplasms/pathology , Child , Child, Preschool , Cohort Studies , Exostoses, Multiple Hereditary/genetics , Female , Genes, Tumor Suppressor/physiology , Growth Disorders/epidemiology , Growth Disorders/genetics , Humans , Incidence , Male , Middle Aged , Osteochondroma/genetics , Prognosis , Radiography , Risk Assessment
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