نتایج جستجو برای: danlos

تعداد نتایج: 3661  

Journal: :The Journal of Nihon University School of Dentistry 1995
A Apaydin

Ehlers-Danlos syndrome (EDS), a group of rare, autosomal dominantly inherited connective tissue dysplasias, characterized mainly by abnormal collagen synthesis, has been shown to exhibit extensive heterogeneity with at least 11 clinical entities differentiated by their clinical, biochemical, and genetic features. Of these, Type VIII EDS is of special interest from a dental viewpoint, due mainly...

Journal: :American journal of medical genetics. Part C, Seminars in medical genetics 2017
Jessica M Bowen Glenda J Sobey Nigel P Burrows Marina Colombi Mark E Lavallee Fransiska Malfait Clair A Francomano

Classical EDS is a heritable disorder of connective tissue. Patients are affected with joint hypermobility, skin hyperextensibilty, and skin fragility leading to atrophic scarring and significant bruising. These clinical features suggest consideration of the diagnosis which then needs to be confirmed, preferably by genetic testing. The most recent criteria for the diagnosis of EDS were devised ...

Journal: :Journal of Dentofacial Anomalies and Orthodontics 2015

Journal: :Sports Health: A Multidisciplinary Approach 2012

Ehlers Danlos syndrome (EDS) is an inherited connective tissue disease due to impaired collagen metabolism. Joint hypermobility and skin hyper extensibility are the major findings. Six types of EDS are recognized. Type I or Gravis type is characterized by skin hyperextensibility, joint hypermobility, skin splitting autosoml dominancy inheritance, preterm premature rupture of membrane (PPROM) an...

Journal: :Orphanet Journal of Rare Diseases 2007

Journal: :Proceedings of the Royal Society of Medicine 1937

Journal: :Proceedings of the Royal Society of Medicine 1968

Journal: :Annals of the Rheumatic Diseases 1994

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