The Association of Myotonia Congenita and Ankylosing Spondylitis

被引：0

作者：

Bagcaci, Sinan ^{[1
]}

Albayrak, Ilknur ^{[2
]}

Karakasli, Sema ^{[3
]}

Kucuksen, Sami ^{[1
]}

Salli, Ali ^{[1
]}

机构：

[1] Necmettin Erbakan Univ, Meram Fac Med, Phys Med & Rehabil Dept, Konya, Turkey

[2] Beysehir Publ Hosp, Phys Med & Rehabil Dept, Beysehir, Konya, Turkey

[3] Minis Hlth Sivas Numune Hosp, Dept Phys Med & Rehabil, Sivas, Turkey

来源：

EUROPEAN JOURNAL OF GENERAL MEDICINE | 2013年 / 10卷 / 01期

关键词：

Ankylosing spondylitis; myotonia congenita; stiffness;

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

This is the first report about the association of ankylosing spondylitis and myotonia congenita. Ankylosing spondylitis is a systemic rheumatologic disease that is characterized by axial skeletal inflammation and accompanied by systemic involvement. The most significant findings of myotonia are the stiffness and the delayed relaxation following the muscle contraction. Both of these pathologies can cause stiffness and also delaying of diagnosis of each other.

引用

页码：63 / 66

页数：4

共 10 条

[1]

BECKER PE, 1977, PATHOGENESIS HUMAN M, P699

[2]

Calabro JJ, 1987, ANKYLOSING SPONDYLIT

[3] Myotonia Congenita and Myotonic Dystrophy: Surveillance and Management [J].

Conravey, Allison ;

Santana-Gould, Lenay .

CURRENT TREATMENT OPTIONS IN NEUROLOGY, 2010, 12 (01) :16-28

[4] Update on spondyloarthropathies [J].

Khan, MA .

ANNALS OF INTERNAL MEDICINE, 2002, 136 (12) :896-907

[5] THE SKELETAL-MUSCLE CHLORIDE CHANNEL IN DOMINANT AND RECESSIVE HUMAN MYOTONIA [J].

KOCH, MC ;

STEINMEYER, K ;

LORENZ, C ;

RICKER, K ;

WOLF, F ;

OTTO, M ;

ZOLL, B ;

LEHMANNHORN, F ;

GRZESCHIK, KH ;

JENTSCH, TJ .

SCIENCE, 1992, 257 (5071) :797-800

[6] AAEE MINIMONOGRAPH .27. DIFFERENTIAL-DIAGNOSIS OF MYOTONIC SYNDROMES [J].

STREIB, EW .

MUSCLE & NERVE, 1987, 10 (07) :603-615

[7] A rare form of painful nondystrophic myotonia [J].

Torbergsen, T ;

Hodnebo, A ;

Brautaset, NJ ;

Loseth, S ;

Stålberg, E .

CLINICAL NEUROPHYSIOLOGY, 2003, 114 (12) :2347-2354

[8]

VANDERLINDEN S, 1984, ARTHRITIS RHEUM, V27, P361

[9]

WHITFIELD AGW, 1979, HDB CLIN NEUROLOGY, V38, P505

[10] Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita [J].

Zhang, J ;

George, AL ;

Griggs, RC ;

Fouad, GT ;

Roberts, J ;

Kwiecinski, H ;

Connolly, AM ;

Ptacek, LJ .

NEUROLOGY, 1996, 47 (04) :993-998

← 1 →