SEDT


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AcronymDefinition
SEDTSocial and Economic Development Trust (India)
SEDTSpondyloepiphyseal Dysplasia Tarda, X-Linked
SEDTSquared Euclidean Distance Transform (computer program)
SEDTSpondylo-Epiphyseal Dysplasia Tarda (premature osteoarthritis)
SEDTSystem Engineering Design Tool (small satellite conceptual design)
SEDTSilver Eagles Drill Team (Michigan State University)
References in periodicals archive ?
Spondyloepiphyseal dysplasia tarda (SEDT) is an X-linked recessive hereditary disease, which was first reported by Gedeon in 1999 [7].
The typical clinical manifestations of SEDT were spinal and skeletal anomalies.
Even so, it is difficult to distinguish SEDT from mucopolysaccharide storage type IV, idiopathic dwarfism, congenital spinal epiphyseal dysplasia, multiple epiphyseal dysplasia, etc., because the clinical features of the disease are not obvious during early childhood [15, 16].
SEDT is a progressive disease, seriously affecting the quality of life of patients, and there is no effective treatment; symptoms are alleviated mostly according to the signs and clinical manifestations of patients, and patients are told to avoid injury to the spinal cord and activities involving the large joints; joint replacement may be considered for severe involvement [17].
Rim et al., "A case of spondyloepiphyseal dysplasia tarda (SEDT) misdiagnosed as ankylosing spondylitis," Journal of Rheumatic Diseases, vol.
Caption: Figure 1: This is the pedigree of a Chinese SEDT family.
Burada spondiloartropati tanisi almis ve osteoporozun eslik ettigi SEDT'li bir olgu sunulacaktir.
Kulac mesafesi boyundan fazla olan, fici gogus ve koksa vara deformitesi ile osteoporozu ve erken dejeneratif degisiklikleri ve vertebral yukseklik kayiplari olan hastaya mevcut bulgu ve semptomlar isiginda SpA tanisi dislanarak SEDT tanisi konuldu.
SED'lerin otozomal dominat kalitim gosteren formlarinin tip 2 kollajen mutasyonuna bagli oldugu (7), SEDT'in X'e bagli resesif kalitim gosteren tipinin ise SEDL proteini gen bolgesindeki mutasyonlara bagli oldugu bildirilmistir.
SEDT'nin tipik olarak X'e bagli kalitim gosteren formunda erkeklerin etkilenmis oldugu, kulac uzunlugunun kisinin boyundan uzun oldugu, fici gogus deformitesi ve erken dejeneratif degisiklikler gorulebilecegi bildirilmistir (2).
SEDT ve osteoporoz birlikteligi sik olmamakla birlikte Turkiye'deki bir yayinda birliktelik bildirilmistir (5).