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Volumn 20, Issue 7, 1998, Pages 507-511

Arthrogryposis multiplex congenita

Author keywords

Causes; Clinical types; Congenital arthrogryposis; Treatment

Indexed keywords

ARTHROGRYPOSIS; BRAIN DISEASE; CHROMOSOME ABERRATION; CONNECTIVE TISSUE DISEASE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTROMYOGRAM; FETUS; FETUS MOVEMENT; HUMAN; MUSCLE BIOPSY; MUSCULAR DYSTROPHY; MYASTHENIA GRAVIS; NEUROPATHY; NEWBORN; ORTHOPEDIC SURGERY; PHYSIOTHERAPY; SHORT SURVEY; UTERUS;

EID: 0031757685     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0387-7604(98)00037-0     Document Type: Article
Times cited : (75)

References (37)
  • 1
    • 0030066811 scopus 로고    scopus 로고
    • Arthrogryposis multiplex congenita, AD 1156
    • Gordon E.C. Arthrogryposis multiplex congenita, AD 1156. Dev Med Child Neurol. 38:1996;80-83.
    • (1996) Dev Med Child Neurol , vol.38 , pp. 80-83
    • Gordon, E.C.1
  • 2
    • 0030930014 scopus 로고    scopus 로고
    • Arthrogryposis multiplex congenita: Etiology, genetics, classification, diagnostic approach, and general aspects
    • Hall J.G. Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspects. J Pediatr Orthop. 6:1997;159-166.
    • (1997) J Pediatr Orthop , vol.6 , pp. 159-166
    • Hall, J.G.1
  • 3
    • 0015322684 scopus 로고
    • 'New' syndrome of congenital contractural arachnodactly originally described by Marfan in 1896
    • Hecht F., Beals R.K. 'New' syndrome of congenital contractural arachnodactly originally described by Marfan in 1896. Pediatrics. 49:1972;574-579.
    • (1972) Pediatrics , vol.49 , pp. 574-579
    • Hecht, F.1    Beals, R.K.2
  • 4
    • 0028077058 scopus 로고
    • Epileptic seizures, arthrogryposis, and migrational brain disorders: A syndrome?
    • Brodtkorb E., Torbergsen T., Nakken K.O.et al. Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome? Acta Neurol Scand. 90:1994;232-240.
    • (1994) Acta Neurol Scand , vol.90 , pp. 232-240
    • Brodtkorb, E.1    Torbergsen, T.2    Nakken, K.O.3
  • 5
    • 0028603613 scopus 로고
    • Lethal arthrogryposis in Finland - A clinical-pathological study of 83 cases during thirteen years
    • Vuopala K., Leisti J., Herva R. Lethal arthrogryposis in Finland - a clinical-pathological study of 83 cases during thirteen years. Neuropediatrics. 25:1994;308-315.
    • (1994) Neuropediatrics , vol.25 , pp. 308-315
    • Vuopala, K.1    Leisti, J.2    Herva, R.3
  • 6
    • 0027362039 scopus 로고
    • Neurogenic arthrogryposis multiplex congenita: Clinical and MRI findings
    • Fedrizzi E., Botteon G., Inverno M.et al. Neurogenic arthrogryposis multiplex congenita: clinical and MRI findings. Pediat Neurol. 9:1993;343-348.
    • (1993) Pediat Neurol , vol.9 , pp. 343-348
    • Fedrizzi, E.1    Botteon, G.2    Inverno, M.3
  • 7
    • 0023122838 scopus 로고
    • Olivo-ponto-cerebellar atrophy with muscular atrophy, joint contractures and pulmonary hypoplasia of prenatal onset
    • Moerman P., Barth P.G. Olivo-ponto-cerebellar atrophy with muscular atrophy, joint contractures and pulmonary hypoplasia of prenatal onset. Virchows Arch A Pathol Anat Histopathol. 410:1987;339-345.
    • (1987) Virchows Arch a Pathol Anat Histopathol , vol.410 , pp. 339-345
    • Moerman, P.1    Barth, P.G.2
  • 8
    • 0021948713 scopus 로고
    • Genetic aspects of arthrogryposis
    • Hall J.G. Genetic aspects of arthrogryposis. Clin Orthop. 194:1985;44-53.
    • (1985) Clin Orthop , vol.194 , pp. 44-53
    • Hall, J.G.1
  • 9
    • 0019471880 scopus 로고
    • Congenital progressive muscular dystrophy of the Fukuyama type-clinical, genetic and pathological considerations
    • Fukuyama Y., Osawa M., Suzuki H. Congenital progressive muscular dystrophy of the Fukuyama type-clinical, genetic and pathological considerations. Brain Dev. 3:1981;1-29.
    • (1981) Brain Dev , vol.3 , pp. 1-29
    • Fukuyama, Y.1    Osawa, M.2    Suzuki, H.3
  • 10
    • 0020695736 scopus 로고
    • Arthrogryposis multiplex congenita. Review with comment
    • Hageman G., Willemse J. Arthrogryposis multiplex congenita. Review with comment. Neuropediatrics. 14:1983;6-11.
    • (1983) Neuropediatrics , vol.14 , pp. 6-11
    • Hageman, G.1    Willemse, J.2
  • 11
    • 0028887824 scopus 로고
    • Lethal arthrogryposis with anterior horn cell disease
    • Vuopala K., Ignatius J., Herva R. Lethal arthrogryposis with anterior horn cell disease. Hum Pathol. 26:1995;12-19.
    • (1995) Hum Pathol , vol.26 , pp. 12-19
    • Vuopala, K.1    Ignatius, J.2    Herva, R.3
  • 12
    • 0030870721 scopus 로고    scopus 로고
    • Arthrogryposis due to infantile neuronal degeneration associated with deletion of the SMNT gene
    • Bingham P.M., Shen N., Rennert H.et al. Arthrogryposis due to infantile neuronal degeneration associated with deletion of the SMNT gene. Neurology. 49:1997;848-851.
    • (1997) Neurology , vol.49 , pp. 848-851
    • Bingham, P.M.1    Shen, N.2    Rennert, H.3
  • 13
    • 0021940015 scopus 로고
    • Neuropathologic aspects of arthrogryposis multiplex congenita
    • Banker B.Q. Neuropathologic aspects of arthrogryposis multiplex congenita. Clin Orthop. 194:1985;30-43.
    • (1985) Clin Orthop , vol.194 , pp. 30-43
    • Banker, B.Q.1
  • 14
    • 0022550695 scopus 로고
    • Arthrogryposis multiplex congenita: Spectrum of pathologic changes
    • Banker B.Q. Arthrogryposis multiplex congenita: spectrum of pathologic changes. Hum Pathol. 17:1986;656-672.
    • (1986) Hum Pathol , vol.17 , pp. 656-672
    • Banker, B.Q.1
  • 15
    • 0016187527 scopus 로고
    • Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex
    • Yuill G.M., Lynch P.G. Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex. J Neurol Neurosurg Psychiatry. 37:1974;316-323.
    • (1974) J Neurol Neurosurg Psychiatry , vol.37 , pp. 316-323
    • Yuill, G.M.1    Lynch, P.G.2
  • 16
    • 0028998066 scopus 로고
    • Arthrogryposis multiplex congenita due to congenital myasthenic syndrome
    • Vajsar J., Sloane A., MacGregor D.L.et al. Arthrogryposis multiplex congenita due to congenital myasthenic syndrome. Pediatr Neurol. 12:1995;237-241.
    • (1995) Pediatr Neurol , vol.12 , pp. 237-241
    • Vajsar, J.1    Sloane, A.2    MacGregor, D.L.3
  • 17
    • 0018856512 scopus 로고
    • Arthrogryposis multiplex congenita due to congenital myasthenia
    • Smit L.M., Barth P.G. Arthrogryposis multiplex congenita due to congenital myasthenia. Dev Med Child Neurol. 22:1980;371-374.
    • (1980) Dev Med Child Neurol , vol.22 , pp. 371-374
    • Smit, L.M.1    Barth, P.G.2
  • 18
    • 0029826644 scopus 로고    scopus 로고
    • Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor function
    • Riemersma S., Vincent A., Beeson D.et al. Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor function. J Clin Invest. 98:1996;2358-2363.
    • (1996) J Clin Invest , vol.98 , pp. 2358-2363
    • Riemersma, S.1    Vincent, A.2    Beeson, D.3
  • 19
    • 0028331166 scopus 로고
    • Lethal congenital muscular dystrophy with arthrogryposis multiplex congenita: Three new cases and review of the literature
    • Sombekke B.H., Molenaar W.M., van Essen A.J., Schoots C.J. Lethal congenital muscular dystrophy with arthrogryposis multiplex congenita: three new cases and review of the literature. Pediartr Pathol. 14:1994;277-285.
    • (1994) Pediartr Pathol , vol.14 , pp. 277-285
    • Sombekke, B.H.1    Molenaar, W.M.2    Van Essen, A.J.3    Schoots, C.J.4
  • 20
    • 0030220198 scopus 로고    scopus 로고
    • Deficiency of a skeletal muscle isoform of α-actinin (α-actinin-3) in merosin-positive congenital muscular dystrophy
    • North K.N., Beggs A.H. Deficiency of a skeletal muscle isoform of α-actinin (α-actinin-3) in merosin-positive congenital muscular dystrophy. Neuromusc Disord. 6:1996;229-235.
    • (1996) Neuromusc Disord , vol.6 , pp. 229-235
    • North, K.N.1    Beggs, A.H.2
  • 21
    • 0030657965 scopus 로고    scopus 로고
    • Ragged-red fibres and complex I deficiency in a neonate with arthrogryposis congenita
    • Laubscher B., Janzer R.C., Krähenbühl S., Hirt L., Deonna T. Ragged-red fibres and complex I deficiency in a neonate with arthrogryposis congenita. Pediat Neurol. 17:1997;249-251.
    • (1997) Pediat Neurol , vol.17 , pp. 249-251
    • Laubscher, B.1    Janzer, R.C.2    Krähenbühl, S.3    Hirt, L.4    Deonna, T.5
  • 22
    • 0020524502 scopus 로고
    • A case of asymmetrical arthrogryposis-a clinical study and a preliminary report on the value of CT scanning
    • Hageman G., Vetre J.K., Willemse J. A case of asymmetrical arthrogryposis-a clinical study and a preliminary report on the value of CT scanning. Brain Dev. 5:1983;407-413.
    • (1983) Brain Dev , vol.5 , pp. 407-413
    • Hageman, G.1    Vetre, J.K.2    Willemse, J.3
  • 23
    • 0030883713 scopus 로고    scopus 로고
    • Arthrogryposis multiplex congenita: Perinatal and electromyographic findings, disability, and psychosocial outcome
    • Södergård J., Hakamies-Blomqvist L., Sainio K., Ryöppy S., Vuorinen R. Arthrogryposis multiplex congenita: perinatal and electromyographic findings, disability, and psychosocial outcome. J Pediatr Orthop. 6:1997;167-171.
    • (1997) J Pediatr Orthop , vol.6 , pp. 167-171
    • Södergård, J.1    Hakamies-Blomqvist, L.2    Sainio, K.3    Ryöppy, S.4    Vuorinen, R.5
  • 24
    • 0029807941 scopus 로고    scopus 로고
    • A revised and extended classification of the distal arthrogryposes
    • Bamshad M., Jorde J.B., Carey J.C. A revised and extended classification of the distal arthrogryposes. Am J Med Genet. 65:1996;277-281.
    • (1996) Am J Med Genet , vol.65 , pp. 277-281
    • Bamshad, M.1    Jorde, J.B.2    Carey, J.C.3
  • 26
    • 0027940224 scopus 로고
    • Arthrogryposis multiplex congenita: A report of two cases
    • Brooks J.G., Coster D.J. Arthrogryposis multiplex congenita: a report of two cases. Aust NZJ Opthalmol. 22:1994;127-132.
    • (1994) Aust NZJ Opthalmol , vol.22 , pp. 127-132
    • Brooks, J.G.1    Coster, D.J.2
  • 27
    • 0030016608 scopus 로고    scopus 로고
    • Familial distal arthrogryposis type 1
    • Stoll C., Alembik Y., Dott B. Familial distal arthrogryposis type 1. Ann Génét. 39:1996;75-80.
    • (1996) Ann Génét , vol.39 , pp. 75-80
    • Stoll, C.1    Alembik, Y.2    Dott, B.3
  • 28
    • 0023783781 scopus 로고
    • The diagnostic management of newborns with congenital contractures: A nosologic study of 75 cases
    • Hageman G., Ippel E.P., Beemer F.A.et al. The diagnostic management of newborns with congenital contractures: a nosologic study of 75 cases. Am J Med Genet. 30:1988;883-904.
    • (1988) Am J Med Genet. , vol.30 , pp. 883-904
    • Hageman, G.1    Ippel, E.P.2    Beemer, F.A.3
  • 29
    • 0020626273 scopus 로고
    • Part 1. Amyoplasia: A common, sporadic condition with congenital contractures
    • Hall J.G., Reed S.D., Driscoll E.P. Part 1. Amyoplasia: a common, sporadic condition with congenital contractures. Am J Med Genet. 15:1983;571-590.
    • (1983) Am J Med Genet , vol.15 , pp. 571-590
    • Hall, J.G.1    Reed, S.D.2    Driscoll, E.P.3
  • 31
    • 0014575512 scopus 로고
    • Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance
    • Gordon H., Davies D., Berman M. Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance. J Med Genet. 6:1969;266-274.
    • (1969) J Med Genet , vol.6 , pp. 266-274
    • Gordon, H.1    Davies, D.2    Berman, M.3
  • 33
    • 0029844409 scopus 로고    scopus 로고
    • Distal arthrogryposis type 1: Clinical analysis of a large kindred
    • Bamshad M., Bohnsack J.F., Jorde L.B., Carey J.C. Distal arthrogryposis type 1: clinical analysis of a large kindred. Am J Med Genet. 65:1996;282-285.
    • (1996) Am J Med Genet , vol.65 , pp. 282-285
    • Bamshad, M.1    Bohnsack, J.F.2    Jorde, L.B.3    Carey, J.C.4
  • 34
    • 0021912374 scopus 로고
    • Arthrogryposis multiplex congenita. A long-term follow-up study
    • Carlson W.O., Speck G.J., Vicari V., Wenger D.R. Arthrogryposis multiplex congenita. A long-term follow-up study. Clin Orthop. 194:1985;115-123.
    • (1985) Clin Orthop , vol.194 , pp. 115-123
    • Carlson, W.O.1    Speck, G.J.2    Vicari, V.3    Wenger, D.R.4
  • 35
    • 0030954971 scopus 로고    scopus 로고
    • The spectrum of arthrogryposis in 33 Chinese children
    • Wong V. The spectrum of arthrogryposis in 33 Chinese children. Brain Dev. 19:1997;187-196.
    • (1997) Brain Dev , vol.19 , pp. 187-196
    • Wong, V.1
  • 36
    • 0030060406 scopus 로고    scopus 로고
    • Amyoplasia, the most common type of arthrogryposis: The potential for good outcome
    • Sells J.M., Jaffe K.M., Hall J.G. Amyoplasia, the most common type of arthrogryposis: the potential for good outcome. Pediatrics. 97:1996;225-231.
    • (1996) Pediatrics , vol.97 , pp. 225-231
    • Sells, J.M.1    Jaffe, K.M.2    Hall, J.G.3
  • 37
    • 0025633696 scopus 로고
    • Arthrogryposis multiplex congenita; Feeding, language and other health problems
    • Robinson R.O. Arthrogryposis multiplex congenita; feeding, language and other health problems. Neuropediatrics. 21:1990;177-178.
    • (1990) Neuropediatrics , vol.21 , pp. 177-178
    • Robinson, R.O.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.