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皮肤僵硬综合征1例 被引量:3

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摘要 皮肤儒硬综合征(stiffskinsyndrome,SSS)可能属于黏多糖病类,又称黏多糖病异型,属于一种罕见的常染色体显性遗传或隐性遗传。临床表现为皮肤变硬,局部色素沉着、毛发增多,关节活动受限。易与硬肿病、嗜酸性筋膜炎、硬斑病等混淆。现报告1例SSS。
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2012年第12期753-754,共2页 Journal of Clinical Dermatology
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参考文献13

  • 1Helm TN, Wirth PB, Helm KF. Congenital fascial dystrophy: thestiff skin syndrome[J]. Cutis, 1997, 60(3): 153-154.
  • 2Esterly NB, Mckusick VA. Stiff skin syndrome [J]. Pediatrics, 1971, 47(2): 360-369.
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二级参考文献15

  • 1崔炳南,刘跃华,孔令荣,王家璧.皮肤僵硬综合征1例[J].临床皮肤科杂志,2005,34(12):818-819. 被引量:3
  • 2[1]Esterly NB,Mckusick VA.Stiff skin syndrome[J].Pediatrics,1971,47(2):360-369.
  • 3[2]Jablonska S,Schubert H,Kikuchi I.Congenital fascial dystrophy:stiff skin syndrome human counterpart of the tight-skin mouse[J].J Am Acad Dermatol,1989,21(5pt1):943-950.
  • 4[3]Fidzianska A,Jablonska S.Congenital fascial dystrophy:abnormal composition of the fascia[J].J Am Acad Dermatol,2000,43(5 Pt 1):797-802.
  • 5[4]Jablonska S,Blaszczyk M.Scleroderma-like indurations involving fascias:an abortive form of congenital fascial dystrophy (Stiff skin syndrome)[J].Pediatr Dermatol,2000,17(2):105-110.
  • 6Esterly NB,McKusick VA.Stiff akin syndrome[J].Pediatrics,1971,47(2):360-369.
  • 7Fidzianska A,Jablonska S.Congenital fascial dystrophy:abnormal composition of the fascia[J].J Am Acad Dermatol,2000,43(5 Pt1):797-802.
  • 8Mat C,Kalayciyan A,Arzuhal N,et al.Stiff akin syndrome:a case report[J].Pediatr Dermatol,2003,20(4):339-341.
  • 9Esterly NB, McKusick VA. Stiff skin syndrome. Pediatrics, 1971, 47: 360-369.
  • 10Jablonska S, Schubert H, Kikuchi I. Congenital fascial dystrophy: stiff skin syndrome-a human counterpart of the tightskin mouse. J Am Acad Dermatol, 1989,21: 943-950.

共引文献12

同被引文献35

  • 1殷文浩,劳力民,郑敏,蔡绥,鲍彰.僵硬皮肤综合征一例[J].中华皮肤科杂志,2003,36(12):723-724. 被引量:3
  • 2颜建华,吴中耀,李永平.特发性眼眶炎性假瘤的神经内分泌调控机制初探[J].眼科研究,2005,23(1):49-51. 被引量:3
  • 3崔炳南,刘跃华,孔令荣,王家璧.皮肤僵硬综合征1例[J].临床皮肤科杂志,2005,34(12):818-819. 被引量:3
  • 4蒲晓英,杨南萍.嗜酸性筋膜炎研究进展[J].现代临床医学,2007,33(2):139-140. 被引量:7
  • 5高亮,杨瑞海,胡宗厚,张传波,王松芬,刘秀玲,刘荣贵.僵硬皮肤综合征[J].临床皮肤科杂志,2007,36(7):445-446. 被引量:2
  • 6Shulman LE. Diffuse faseiitis with hypergammagtobulinemia and eosinophilia: a new syndrome[J]. J Rheumatol, 1984, 11(5): 569-570.
  • 7Lakhanpal S, Ginsburg WW, Michet CJ, et al. Eosinophilic fasciitis: clinical spectrum and therapeutic response in 52 cases [J]. Semin Arthritis Rheum, 1988, 17(4): 221-231.
  • 8Bischoff L, Derk CT. Eosinophilic fasciitis: demographics, dis- ease pattern and response to treatment: report of 12 cases and review of the literature[J]. Int J Dermatol, 2008, 47(1): 29-35.
  • 9Lebaux D, S~ne D. Eosinophilic fasciitis (Shulman disease)[J]. Best Pract Res Clin Rheumatol, 2012, 26(4): 449-458.
  • 10TralleruAaguas E, Selva O' Callaghan A, Simeon Aznar CP, et al. Eosinophilic fasciitis: analysis of a series of 10 patients[J]. Med Clin (Barc), 2005, 125(4): 145-148.

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