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Volumn 33, Issue 11, 2013, Pages 1102-1104

The role of ultrasound in fetal congenital myopathy detection: A novel case of fetal-onset cap myopathy

Author keywords

[No Author keywords available]

Indexed keywords

BETAMETHASONE SODIUM PHOSPHATE; SULINDAC;

EID: 84886594874     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.4184     Document Type: Letter
Times cited : (1)

References (8)
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    • Sharma MC, Jain D, Sarkar C et al. Congenital myopathies - a comprehensive update of recent advancements. Acta Neuroligica Scandinavica 2009;119:281-2922.
    • (2009) Acta Neuroligica Scandinavica , vol.119 , pp. 281-2922
    • Sharma, M.C.1    Jain, D.2    Sarkar, C.3
  • 2
    • 0031736853 scopus 로고    scopus 로고
    • Congenital rapidly fatal form of nemaline myopathy with fetal hydrops and arthrogryposis. A case report and review
    • Vardon D, Chau C, Sigodi S et al. Congenital rapidly fatal form of nemaline myopathy with fetal hydrops and arthrogryposis. A case report and review. Fetal Diagnos Ther 1998;13(4):244-9.
    • (1998) Fetal Diagnos Ther , vol.13 , Issue.4 , pp. 244-249
    • Vardon, D.1    Chau, C.2    Sigodi, S.3
  • 3
    • 0037110998 scopus 로고    scopus 로고
    • Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnoses
    • Witters I, Moerman P, Fryns, JP. Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnoses. Am J Med Genet 2002;113:23-8.
    • (2002) Am J Med Genet , vol.113 , pp. 23-28
    • Witters, I.1    Moerman, P.2    Fryns, J.P.3
  • 4
    • 70649113040 scopus 로고    scopus 로고
    • Serial postural and motor assessment of fetal akinesia deformation sequence (FADS)
    • Donker M
    • Donker M, Eijckelhof BH, Tan GM et al. Serial postural and motor assessment of fetal akinesia deformation sequence (FADS). Early Hum Dev 2009; 85(12):785-90.
    • (2009) Early Hum Dev , vol.85 , Issue.12 , pp. 785-790
    • Eijckelhof, B.H.1    Tan, G.M.2
  • 5
    • 0034831131 scopus 로고    scopus 로고
    • Fetal akinesia deformation sequence: behavioural development in a case of congenital myopathy
    • Mulder EJ, Nikkels PG, Visser GH. Fetal akinesia deformation sequence: behavioural development in a case of congenital myopathy. Ultrasound in obstetrics and gynaecology 2001;18(3):253-7.
    • (2001) Ultrasound in obstetrics and gynaecology , vol.18 , Issue.3 , pp. 253-257
    • Mulder, E.J.1    Nikkels, P.G.2    Visser, G.H.3
  • 6
    • 77955972479 scopus 로고    scopus 로고
    • Mutation studies in X-linked myotubular myopathy in three Indian families
    • Bijarnia S, Puri RD, Jain M et al. Mutation studies in X-linked myotubular myopathy in three Indian families. Indian J Pediatr 2010;77(4):431-3.
    • (2010) Indian J Pediatr , vol.77 , Issue.4 , pp. 431-433
    • Bijarnia, S.1    Puri, R.D.2    Jain, M.3
  • 7
    • 55149093405 scopus 로고    scopus 로고
    • Utility of fetal muscle biopsy for diagnosis of nemaline myopathy
    • et al.
    • Kasperski SB, Brennan AM, Corteville et al. Utility of fetal muscle biopsy for diagnosis of nemaline myopathy. Fetal Diagnosis and Therapy 2008;24(4):400-4.
    • (2008) Fetal Diagnosis and Therapy , vol.24 , Issue.4 , pp. 400-404
    • Kasperski, S.B.1    Brennan, A.M.2    Corteville3
  • 8
    • 67349255416 scopus 로고    scopus 로고
    • Cap disease due to mutation of the beta-tropomyosin gene (TPM2)
    • Clarke NF, Domazetovska A, Waddell L et al. Cap disease due to mutation of the beta-tropomyosin gene (TPM2). Neuromuscul Disord 2009;19(5):348-51.
    • (2009) Neuromuscul Disord , vol.19 , Issue.5 , pp. 348-351
    • Clarke, N.F.1    Domazetovska, A.2    Waddell, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.