翻訳と辞書
Words near each other
・ Autostrada A19 (Italy)
・ Autostrada A20 (Italy)
・ Autostrada A21 (Italy)
・ Autostrada A22 (Italy)
・ Autostrada A23 (Italy)
・ Autostrada A24 (Italy)
・ Autostrada A25 (Italy)
・ Autostrada A26 (Italy)
・ Autostrada A27 (Italy)
・ Autostrada A28 (Italy)
・ Autostrada A29 (Italy)
・ Autostrada A3 (Italy)
・ Autostrada A30 (Italy)
・ Autostrada A31 (Italy)
・ Autosomal recessive cerebellar ataxia
Autosomal recessive multiple epiphyseal dysplasia
・ Autosomal recessive polycystic kidney disease
・ Autosome
・ Autosphyla
・ Autosplenectomy
・ Autospore
・ Autosport
・ Autosport Awards
・ Autosport International
・ Autosports India
・ Autostade
・ Autostadt
・ Autostereogram
・ Autostereoscopy
・ Autosticha


Dictionary Lists
翻訳と辞書 辞書検索 [ 開発暫定版 ]
スポンサード リンク

Autosomal recessive multiple epiphyseal dysplasia : ウィキペディア英語版
Autosomal recessive multiple epiphyseal dysplasia

Autosomal recessive multiple epiphyseal dysplasia (ARMED), also called epiphyseal dysplasia, multiple, 4 (EDM4), multiple epiphyseal dysplasia with clubfoot or –with bilayered patellae, is an autosomal recessive congenital disorder affecting cartilage and bone development. The disorder has relatively mild signs and symptoms, including joint pain, scoliosis, and malformations of the hands, feet, and knees.〔(【引用サイトリンク】title=Recessive multiple epiphyseal dysplasia at Genetics Home Reference )
Some affected individuals are born with an inward- and downward-turning foot (a clubfoot). An abnormality of the kneecap called a double-layered patella is also relatively common. Although some people with recessive multiple epiphyseal dysplasia have short stature as adults, most are of normal height. The incidence is unknown as many cases are not diagnosed due to mild symptoms.
== Cause and Genetics ==

Mutations in the SLC26A2 (DTDST) gene, located at human chromosome 5q32-33.1, are the cause of ARMED.〔 It is considered a milder disorder within a spectrum of skeletal disorders caused by mutations in the gene, which encodes a protein that is essential for the normal development of cartilage and its conversion to bone.〔 Mutations in the SLC26A2 gene alter the structure of developing cartilage, preventing bones from forming properly and resulting in associated skeletal maldevelopment.〔
The disorder is inherited in an autosomal recessive manner.〔 This means the defective gene responsible for the disorder is located on an autosome (chromosome 5 is an autosome), and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder. The parents of an individual with an autosomal recessive disorder both carry one copy of the defective gene, but usually do not experience any signs or symptoms of the disorder.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Autosomal recessive multiple epiphyseal dysplasia」の詳細全文を読む



スポンサード リンク
翻訳と辞書 : 翻訳のためのインターネットリソース

Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.