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儿童非肌性肌球蛋白重链9基因相关血小板减少性疾病诊断与治疗 被引量:1

Diagnosis and treatment advances of MYH9-associated diseases in children
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摘要 非肌性肌球蛋白重链9基因相关疾病(nonmuscle myosin heavy chain 9 related disease,MYH9-RD)是MYH9基因突变引起的遗传性血小板减少性疾病,为常染色体显性遗传。患儿自出生起即表现为巨大血小板减少症,症状常伴随终生。通常表现为轻微出血症状,但因临床对该病认识不足,患儿常被漏诊或误诊为慢性免疫性血小板减少性紫癜(ITP),给予不必要甚至有害的治疗,造成不良预后。为避免这种情况发生,本文就儿童MYH9-RD诊断治疗进展做一阐述。
作者 崔颖慧 于洁
出处 《中国实用儿科杂志》 CSCD 北大核心 2013年第9期673-675,共3页 Chinese Journal of Practical Pediatrics
关键词 非肌性肌球蛋白重链9基因 免疫性血小板减少性紫癜 血小板减少症 儿童 nonmuscle myosin heavy chain 9(MYH9) immune thrombocytopenia(ITP) thrombocytopenia child
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参考文献14

  • 1Pecci A, Panza E, Pujol-Moix N, et al.Position of Nonmuscle Myosin Heavy Chain IIA (NMMHC-IIA) Mutations Predicts the Natural History of MYH9-Related Disease [J].Hum Mut, 2008,29 ( 3 ) : 409-417.
  • 2Noris P, Pecci A, Di Bari F, et al.Application of a diagnostic al- gorithm for inherited thrombocytopenias to 46 consecutive pa- tients [ J ].Haematologica, 2004,89 : 1219-1225.
  • 3Althaus K, Greinacher A.MYH9-Related Platelet Disorders [J ]. Semin Thromb Hemost, 2009,35 (2) : 189-203.
  • 4Geddis AE, Kaushansky K.Inherited thrombocytopenias: toward a molecular understanding of disorders of platelet production [ J]. Curt" Opin Pediatr, 2004,16( 1 ) : 15-22.
  • 5Vicente-Manzanares M, Ma X, Adelstein RS, et al.Non-muscle myosin II takes centre stage in cell adhesion and migration [J]. Nat Rev Molecul Cell Biol, 2009,10 : 778-790.
  • 6Heath KE, Campos-Barros A, Toren A, et al.Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal domi- nant macrothrombocytopenias : May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes [J]. Am J Hum Genet,2001,11,69(5 ) : 1033-1045.
  • 7Leung TF, Tsoi WC, Li CK, et al.A Chinese adolescent girl with Fechtner-like syndrome[J].Acta Paediatr, 1998,87:705-707.
  • 8Bostrom MA, Freedman BI.The Spectrum of MYH9-Associated Nephropathy[ J] .Clin J Am Soc Nephrol, 2010,5 : 1107-1113.
  • 9Revel-Vilk S, Rand ML.An Approach to the Diagnosis of Mild and Moderate Bleeding Disorders in Children [J].Journal Of Co- agulation Disorders, 2010: 1-6.
  • 10Israels SJ, Kahr WHA, Blanchette VS, et al.Platelet Disorders in Children: A Diagnostic Approach[J].Pediatr Blood Cancer, 2011,56:975-983.

二级参考文献9

  • 1Kunishima S, Kojima T, Matsushita T, et al. Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/sebastian syndrome). Blood, 2001, 97:1147-1149.
  • 2Kelley MJ, Jawien W, Ortel TL, et al. Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. Nat Genet, 2000, 26:106-108.
  • 3Seri M, Cusano R, Gangarossa S, et al. Mutations in MYH9 result in the May-Hegglin anomaly, and fechtner and sebastian syndromes. The May-Heggllin/fechtner syndrome consortium. Nat Genet, 2000, 26:103-105.
  • 4Cawley JC, Hayhoe FG. The inclusions of the May-Hegglin anomaly and Dohle bodies of infection: an ultrastructural comparison. Br J Hematol, 1972, 22:491-496.
  • 5Pecci A, Noris P, Invernizzi R, et al. Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders.Br J Haematol, 2002,117:164-167.
  • 6Kunishima S, Matsushita T, Kojima T, et al. Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations. Lab Invest, 2003, 83: 115-122.
  • 7Sellers JR. Myosins: a diverse superfamily. Biochim Biophys Acta, 2000, 1496: 3-22.
  • 8徐敏,凌柱三,张广森,吴晓英,张淑安.May-Hegglin异常二例[J].中华血液学杂志,2001,22(3):152-153. 被引量:23
  • 9张广森,易彦,徐敏,凌柱三.一个May-Hegglin异常家系非肌性肌球蛋白重链9基因突变位点的鉴定[J].中华医学杂志,2002,82(13):918-920. 被引量:17

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