همراهی سندرم دی جورج با رماتیسم ایدیوپاتیک نوجوانان

صالح زاده, فرهاد and باقری, امين (1393) همراهی سندرم دی جورج با رماتیسم ایدیوپاتیک نوجوانان. Iranian Journal of Pediatrics ــ 24 (3). pp. 334-335. شاپا 2008-2142

Text - Published Version

Official URL: http://ijp.tums.ac.ir/index.php/ijp/article/view/1...


Association of juvenile idiopathic arthritis and digeorge syndrome; a case report

English Abstract

Juvenile idiopathic arthritis (JIA) belongs to a group of arthritis with unknown etiology that occurs in children under 16 years old. Pathogenesis of this disease proposes the role of autoimmune process which is induced by antigens and results in inflammation of synovials and cartilage[1]. DiGeorge syndrome (DGS) or velo-cardio-facialsyndrome (VCFS) is a genetic disorder due to a defect in 22q11.2 chromosome[2]. Patients with 22q11.2 DS usually have characteristic facies including retrognathia or micrognathia, long face, downturned mouth, short philtrum low-set, malformed ears and hypertelorism. Congenital heart defects, either a cleft palate or incompetence of the soft palate, and immune deficiencies are common. Patients may have short stature and occasional instances of growth hormone

Item Type:Article
زبان سند : انگلیسی
نویسنده مسئول :فرهاد صالح زاده
نویسنده :امين باقری
Additional Information:IF: 0.258 Indexing & Abstracting: ISI (Citation Index Expanded); PUBMED and PUBMED Central; SCOPUS; Embase; CINAHL; Bioline International Website; Global Health; DOAJ; IMMER; National Library for Health; SID; Iranmedex; Magiran; EMRMedex; Genamics-JournalSeek; Index Copernicus; MedBioWorld; Nutrition and Food Sciences; Open J-Gate; Ulrich Database; SJSU; EZB
کلیدواژه ها (انگلیسی):Digeorge Syndrome; Juvenile Idiopathic Arthritis; Velocardiofacial Syndrome
Subjects:WS Pediatrics
Divisions:Faculty of Medicine > Department of Pediatrics , Community Medicine
ID Code:6128
Deposited By: MS Soghra Golmaghani
Deposited On:04 Dec 1393 06:03
Last Modified:04 Dec 1393 06:06

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