Searchable abstracts of presentations at key conferences on calcified tissues

ba0006p174 | (1) | ICCBH2017

Maffucci syndrome – as an extremely rare form of Ollier disease

Molnar Inna , Guk Yuriy

Present a clinical case of Maffuchchi Syndrome and highlight its clinical and orthopedic features and differences from the Ollier disease Methods: Risk of secondary chondrosaroma higher at Maffuchchi syndrome – 46%. Almost 100% extraskeletal malignant transformation compared to Ollier disease which, according to various estimates, is 5–43% of all cases. Maffuchchi syndrome is a rare (‘orphan’) disease, and therefore not well known by scientists and practici...

ba0006p173 | (1) | ICCBH2017

Results of surgical treatment of tibia deformity in patients with Campanaccis disease

Guk Yuriy , Zyma Andrii , Cheverda Andrii , Oliinyk Yuriy , Demyan Yuriy

Relevance of the study due to progressive and opportunity of Campanaccis disease to relapse after surgical treatment. Analysis of surgical treatment of seven patients with osteo-fibrous dysplasia of tibia (four male, three – female) aged 2–17 years who performed 13 surgeries. Bone grafting after curettage residual cavities made in two of seven patients, including allografts used in one patient, ceramic hydroxyapatite ‘Kerhap’ – in two patients, with on...

ba0006p026 | (1) | ICCBH2017

Own research experience of bone tissue metabolism in patients with the Ehlers-Danlos syndrome

Demyan Yuriy , Guk Iurii , Magomedov Oleksandr , Zyma Andrii , Cheverda Andrii , Polishchuk Tamara Kincha , Balacka Natalia

Purpose: To explore the features of bone metabolism and create a system of medical correction of violations in patients with Ehlers-Danlos syndrome.Materials and methods: Based on the analysis of the survey results of 12 patients with different types of EDS aged 3 to 10 years (males - 8 patients, female - 4 patients) who were treated in Institute of Orthopedics and Traumatology,National Academy of Medical Sciences, Kiev, Ukraine from 2005 to 2015 years. ...