vspВопросы современной педиатрииCurrent Pediatrics1682-55271682-5535Издательство «ПедиатрЪ»vsp-1410Research ArticleКЛИНИЧЕСКИЕ НАБЛЮДЕНИЯCLINICAL OBSERVATIONSСПОНТАННОЕ РАССАСЫВАНИЕ МЕТАКАРПАЛЬНЫХ И МЕТАТАРЗАЛЬНЫХ КОСТЕЙ В ПРАКТИКЕ ДЕТСКОГО РЕВМАТОЛОГАSPONTANEOUS CARPAL TARSAL OSTEOLYSIS IN CHILDREN'S RHEUMATOLOGIST PRACTICEЖолобоваЕ.С.ZholobovaE.S.БобылеваВ.Н.BobylevaV.N.МихалеваГ.В.MikhalevaG.V.Московская медицинская академия им. И.М. СеченоваРоссияI.M. Sechenov Moscow Medical AcademyRussian Federation20080511201573Вопросы современной педиатрии113116Copyright © Жолобова Е., Бобылева В., Михалева Г., 20082008Жолобова Е., Бобылева В., Михалева Г.Zholobova E., Bobyleva V., Mikhaleva G.Данная работа распространяется под лицензией Creative Commons Attribution 4.0.This work is licensed under a Creative Commons Attribution 4.0 License.https://vsp.spr-journal.ru/jour/article/view/1410ReferencesEisenstein D.M., Poznanski A.K.,Pachman L.M. Torg osteolysis syndrom. Am. J. Med. Genet. 1998; 16 (80): 207–212.Eisenstein D.M., Poznanski A.K.,Pachman L.M. Torg osteolysis syndrom. Am. J. Med. Genet. 1998; 16 (80): 207–212.Al Aqeel A., Al Sewairi W., Edress B. et al. Inherited multicentric osteolysis with arthritis: a variant resembling Torg syndrome in a Saudi family. Am. J. Med. Genet. 2000; 3 (93): 11–18.Al Aqeel A., Al Sewairi W., Edress B. et al. Inherited multicentric osteolysis with arthritis: a variant resembling Torg syndrome in a Saudi family. Am. J. Med. Genet. 2000; 3 (93): 11–18.Zankl A., Pachman L., Poznanski A. et al. Torg syndrome is caused by inactivating mutations in MMP2 and is allelic to NAO and Winchester syndrome. J. Bone Miner Res. 2007; 22 (2): 329–333.Zankl A., Pachman L., Poznanski A. et al. Torg syndrome is caused by inactivating mutations in MMP2 and is allelic to NAO and Winchester syndrome. J. Bone Miner Res. 2007; 22 (2): 329–333.Rouzier C., Vanatka R., Bannwarth S. et al. A novel homozygous MMP2 mutation in a family with Winchester syndrome. Clin. Genet. 2006; 69 (3): 271–276.Rouzier C., Vanatka R., Bannwarth S. et al. A novel homozygous MMP2 mutation in a family with Winchester syndrome. Clin. Genet. 2006; 69 (3): 271–276.Singh J.A., Williams C.B., McAlister W.H. Talo–patella scaphoid osteolysis, synovitis, and short fourth metacarpals in sisters: a new syndrome? Am. J. Med. Genet. A. 2003; 30 (121): 118-125.Singh J.A., Williams C.B., McAlister W.H. Talo–patella scaphoid osteolysis, synovitis, and short fourth metacarpals in sisters: a new syndrome? Am. J. Med. Genet. A. 2003; 30 (121): 118-125.Faber M.R., Verlaak R., Fiselier T.J. et. al. Inherited multicentric osteolysis with carpal-tarsal localization, mimicking juvenile idiopathic arthritis. Eur. J. Pediatr. 2004; 163 (10): 612-618.Faber M.R., Verlaak R., Fiselier T.J. et. al. Inherited multicentric osteolysis with carpal-tarsal localization, mimicking juvenile idiopathic arthritis. Eur. J. Pediatr. 2004; 163 (10): 612-618.
The authors declare that there are no conflicts of interest present.