期刊文献+

先天性无痛无汗症并发习惯性髋关节脱位1例 被引量:2

Congenital insensitivity to pain with anhidrosis combined with habituation hip joint dislocation:a case report
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摘要 先天性无痛无汗症(congenital insensitivity to pain with anhidrosis,CIPA)又称遗传性感觉和自主神经障碍(HSAN)IV型,是一种罕见病^[1-2]。本病属常染色体隐性遗传性疾病,首先由Dearbom(1932年)报道。国外报道了近40例,国内报道20余例,临床表现为感觉障碍,包括痛觉和温度觉、无汗、
出处 《中国骨伤》 CAS 2010年第5期388-389,共2页 China Journal of Orthopaedics and Traumatology
关键词 痛觉缺失 先天性 少汗症 髋脱位 病例报告 Pain insensitivity,congenital Hypohidrosis Hip dialocation Case reports
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参考文献8

  • 1Dyck PJ,Mellinger JF,Reagan CJ,et al.Not indifference to pain but varieties of hereditary sensory and autonomic neuropathy.Brain,1983,106:373-390.
  • 2Hilz MJ.Assessment and evaluation of hereditary sensory and autonomic neuropathies with autonomic and neurophysiological examinations.Clin Auton Res,2002,12(Suppl 1):133-143.
  • 3Sztriha L,Lestringant GG,Hertecant J,et al.Congenital insensitivity to pain with anhidrosis.Pediatr Neurol,2001,25:63-66.
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  • 5董平,刘京升.先天性无痛无汗症并习惯性髋关节脱位一例[J].中国全科医学,2008,11(5):423-423. 被引量:3
  • 6Schulman H,Tsodikow V,Einhorn M,et al.Congenital insensitivity to pain with anhidiosis(CIPA):the spectum of radiological findings.Pediatr Radiol,2001,31:701-705.
  • 7李玉清,丁建平,张泽坤,王溱.先天性无痛无汗症骨关节改变二例[J].临床放射学杂志,2008,27(9):1260-1261. 被引量:6
  • 8沈品泉,陆美玲,张菁.遗传性感觉和自主神经障碍Ⅳ型导致儿童Charcot关节病[J].临床骨科杂志,2005,8(5):405-406. 被引量:5

二级参考文献18

  • 1沈品泉,陆美玲,张菁.遗传性感觉和自主神经障碍Ⅳ型导致儿童Charcot关节病[J].临床骨科杂志,2005,8(5):405-406. 被引量:5
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  • 5Bonkowsky JL, Johnson J, Carey JC, et al. An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis[J]. Pediatrics,2003,112(3 Pt 1): 237~41.
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  • 7Dyck Pj, Mellinger IF, Horowitz SJ, et al. Nofindeference to pain but varicetics of hereditary sensory, and autonomic neuropathy[ J]. Brain, 1983, 106: 373-390.
  • 8Snanson NA, Argental LC, Aslanidis C, et al. Tissue expansion. University of Michigan Mdical Center[ J].Adv Dermatol, 1988,3 : 243 - 246.
  • 9Matsuo T, Shinazawa H, Sugahara K, et al. Clinical and electeomyographic findings in a transitional form of sporadic acrodystrophic neuropathy [J]. Am J DIS Child, 1979, 133: 1153.
  • 10Bonkowsky JL, Johnson J, Carey JC, et al. An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRKI gene causing congenital insensitivity to pain with anhidrosis [J]. Pediatrics, 2003, 112: 237 - 241.

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