Searchable abstracts of presentations at key conferences on calcified tissues

ba0003pp183 | Chondrocytes and cartilage | ECTS2014

Meniscus – Cartilage paracrine crosstalk in osteoarthritis

Samara Stavroula , Chatzopoulou Elisavet , Melas Ioannis , Messinis Dimitris , Dailiana Zoe , Kollia Panagoula , Alexopoulos Leonidas

Introduction: Meniscus plays an essential role in knee joint function providing stability and load transmission. In osteoarthritis (OA), a joint disease characterized by chronic synovitis and cartilage degeneration, pathological changes in the menisci are observed. However, whether menisci contribute to the progression of OA, the underlying mechanism for meniscus-cartilage communication is still unclear. In this study we analyzed systematically the response of meniscus and car...

ba0001pp6 | Clinical case posters | ECTS2013

Diagnosis of fibrous dysplasia with DNA tests

Stathopoulos Ioannis , Balanika Alexia , Baltas Christos , Lampropoulou-Adamidou Kalliopi , Koromila Theodora , Kollia Panagoula , Tournis Symeon , Papaioannou Nikolaos , Katsalira Aikaterini

Introduction: Fibrous dysplasia (FD) of bone is a benign, non-inheritable disease characterized by bone pain, bone deformities and fractures. Its prevalence is ~1 in 30 000 individuals and diagnosis is based on the clinical and radiologic findings and is confirmed by biopsy. Yet, in some cases biopsy is not applicable.Case report: A young woman presented to our outpatient clinic with a history of pain localized at the distal half of the left tibia that h...

ba0001pp5 | Clinical case posters | ECTS2013

Late onset autosomal dominant hypophosphatemic rickets; confirmation of the diagnosis with genomic analysis

Tournis Symeon , Stathopoulos Ioannis , Lampropoulou-Adamidou Kalliopi , Koromila Theodora , Chatzistamatas Nikolaos , Droggaris Michail , Zafeiris Christos , Makris Konstantinos , Marketou Helen , Papaioannou Nikolaos , Kollia Panagoula , Gazi Gazi

Introduction: Autosomal dominant hypophosphatemic rickets (ADHR) is a rare form of inherited isolated renal phosphate wasting with two distinct clinical phenotypes; early-onset and late-onset. Late-onset ADHR is characterized by normal phosphate levels and growth during childhood, followed by osteomalacia with bone pain, pseudofractures and weakness in adolescence or adulthood, but with no lower extremity deformities. Most of the late-onset ADHR patients are women and pregnanc...