Academic Journal

Aarskog-Scott syndrome: An unusual cause of scoliosis

التفاصيل البيبلوغرافية
العنوان: Aarskog-Scott syndrome: An unusual cause of scoliosis
المؤلفون: Kerim Sariyilmaz, Okan Ozkunt, Murat Korkmaz, Fatih Dikici, Unsal Domanic
المصدر: Journal of Craniovertebral Junction and Spine, Vol 8, Iss 3, Pp 283-284 (2017)
بيانات النشر: Wolters Kluwer Medknow Publications
سنة النشر: 2017
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Aarskog-scott syndrome, scoliosis, spinal deformity, Diseases of the musculoskeletal system, RC925-935
الوصف: A 16-year-old boy who had been diagnosed previously as Aarskog-Scott syndrome (AAS), referred to our clinic with shoulder asymmetry for 1 year. Results of spine examination showed a 52° right thoracic curve at T3-T11. Surgery was planned, and T1–L1 posterior instrumentation and fusion were performed. After surgery, satisfactory correction was achieved, and during 10 years follow-up, the patient had no complaints. AAS is a X-linked genetic disorder with facial, genital, and skeletal manifestations. Scoliosis is not reported as a typical finding of AAS, and there is no reported case in the English literature. Due to mutation affecting the developing skeleton tissue, spinal deformities may develop. In our case, concave side fusion was seen at the deformity. Although we do not know any specific pattern of the scoliotic deformity of this syndrome, surgical correction of the deformity can be difficult because of the premature fusion at these levels.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0974-8237
Relation: http://www.jcvjs.com/article.asp?issn=0974-8237;year=2017;volume=8;issue=3;spage=283;epage=284;aulast=Sariyilmaz; https://doaj.org/toc/0974-8237; https://doaj.org/article/f6050b7bbfbf4fd4b5a678efa74b7713
DOI: 10.4103/jcvjs.JCVJS_133_16
الاتاحة: https://doi.org/10.4103/jcvjs.JCVJS_133_16
https://doaj.org/article/f6050b7bbfbf4fd4b5a678efa74b7713
رقم الانضمام: edsbas.F8A35D98
قاعدة البيانات: BASE
الوصف
تدمد:09748237
DOI:10.4103/jcvjs.JCVJS_133_16