| Literature DB >> 7492165 |
B Lubec1, I Steinert, F Breier, W Jurecka, K Pillwein, S Fang-Kircher.
Abstract
Juvenile hyaline fibromatosis is a rare disorder characterised by multiple subcutaneous tumours, gum hypertrophy, muscle weakness, and flexion contractures of the large joints. Histology shows an abundance of a homogenous, amorphous, acidophilic extracellular matrix in which spindle shaped cells are embedded forming minute streaks. It has been previously suggested that collagen abnormalities may be involved. A 14 month old girl with this syndrome is described in whom postmortem western blot studies were performed. These studies revealed an absent pro-alpha 2(I) chain and an absent collagen type III chain in skin but not in the other organs examined.Entities:
Mesh:
Year: 1995 PMID: 7492165 PMCID: PMC1511266 DOI: 10.1136/adc.73.3.246
Source DB: PubMed Journal: Arch Dis Child ISSN: 0003-9888 Impact factor: 3.791