| Literature DB >> 19921528 |
Giacomo Sabbioni1, Nicola Rani, Valentina Devescovi.
Abstract
The case of a 3-year-old child diagnosed with Type 1 neurofibromatosis is presented, showing pigmented birthmarks and gigantism of the left lower limb associated with the presence of multiple neurofibromas. Increased bone growth appears to be the direct or indirect consequence of a still undefined paracrine effect of nerve tumor cells.Entities:
Mesh:
Year: 2009 PMID: 19921528 DOI: 10.1007/s12306-009-0049-8
Source DB: PubMed Journal: Musculoskelet Surg ISSN: 2035-5114