相关期刊:《World Journal of Cardiology》《World Journal of Medical Genetics》《Journal of Biomedical Science and Engineering》《Journal of Biosciences and Medicines》更多>>
Introduction:People are now presenting with chronic musculoskeletal pain at a younger age,and many of them fulfil criteria for fibromyalgia.We have recently shown a strong association between fibromyalgia symptoms and...
Introduction: A new electromechanical instrument has been developed to measure relative dorsal mobility of the first ray in an objective and reliable way by simulating ground reaction forces during gait. This device e...
Purpose: To alert the medical community that whole exome sequencing can find accessory gene changes in well-known syndromes that alter preventive health care and management. Meaning: A collagen type VI gene change add...
Intricate and reproducible patterning of root tissues is critical for root function and plant survival.In particular,patterning of the ground tissue(endodermis and cortex)is vital to regulating mate-rial exchange and ...
the National Institute of Child Health and Human Development,No.HD02528。
Ehlers-Danlos syndrome(EDS)is a heterogeneous group of connective tissue disorders comprised of several types.Classic EDS is an autosomal dominant disorder with stretchable skin,delayed wound healing with poor scarrin...
Findings in 1656 patients referred for evaluation of Ehlers-Danlos syndrome, 710 evaluated systematically using novel history and physical forms, defined a characteristic clinical pattern termed arthritis-adrenaline d...
supported by the 90th Anniversary of Chulalongkorn University,Rachadapisek Sompote Fund;Faculty of Dentistry(DFR62003),Chulalongkorn University;Chulalongkorn Academic Advancement Into Its 2nd Century Project;Newton Fund;Thailand Research Fund(RSA6280001,DPG6180001);supported by Ratchadapisek Somphot Fund for Postdoctoral Fellowship,Chulalongkorn University,Thailand。
Osteogenesis imperfecta(OI)is mainly characterized by bone fragility and Ehlers-Danlos syndrome(EDS)by connective tissue defects.Mutations in COL1A1 or COL1A2 can lead to both syndromes.OI/EDS overlap syndrome is most...
Joint hypermobility syndrome is a condition in which a joint can move effortlessly beyond the normal limit of motion expected for that joint. This syndrome is affected by some factors including gender and tends to be ...
Supported by The National Institute of Child Health and Human Development(NICHD),No.HD02528
We report a 28-year-old female who presented with severe joint pain, chronic muscle weakness, Raynaud’s phenomenon, and hypermobility. She was found to have a 6074A 〉 T nucleotide transition in the TNXB gene causing...