Abstract
We report a new disorder that we have called genochondromatosis. Four patients from the same family with the characteristic localisation of chondromatosis (clavicle, upper end of humerus, and lower end of femur) were investigated. The favourable course, the dominant transmission, and previous publication of similar cases confirm the uniqueness of this new entity. The chondrodysplasias with disorganised development of cartilage are far from being completely understood. Recently, several disorders within this group have been well defined, including metachondromatosis and spondyloenchondroplasia, but there still remain numerous clinical subgroups that are very difficult to classify.
Full text
PDFImages in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- LAMY M., AUSSANNAIRE M., JAMMET M. L., NEZELOF C. Trois cas de maladie d'Ollier dans une fratrie. 1954 Jan 29-Feb 5Bull Mem Soc Med Hop Paris. 70(3-4):62–70. [PubMed] [Google Scholar]
- MAROTEAUX P., LAMY M. [Dyschondroplasia. Multiple chondromatosis of the skeleton]. Sem Hop. 1960 Jan 18;36:182–93/SP. [PubMed] [Google Scholar]
- Maroteaux P. La metachondromatose. Z Kinderheilkd. 1971;109(3):246–261. [PubMed] [Google Scholar]
- ROSSBERG A. Zur Erblichkeit der Knochenchondrome. Fortschr Geb Rontgenstr Nuklearmed. 1959 Jan;90(1):138–139. [PubMed] [Google Scholar]