Research ArticlePEDIATRICS
MR Imaging Findings in Children with Merosin-Deficient Congenital Muscular Dystrophy
Pilar A. Caro, Mena Scavina, Eric Hoffman, Elena Pegoraro and Harold G. Marks
American Journal of Neuroradiology February 1999, 20 (2) 324-326;
Pilar A. Caro
Mena Scavina
Eric Hoffman
Elena Pegoraro
References
- ↵Tome FM, Evangelista T, Leclerc A, et al. Congenital muscular dystrophy with merosin deficiency. C R Acad Sci III 1994;317:351-357
- ↵Leyten QH, Gabreels FJ, Renier WO, et al. White matter abnormalities in congenital muscular dystrophy. J Neurol Sci 1995;129:162-169
- ↵Trevisan CP, Martinello F, Ferruzza E, Angelini C. Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up. Eur Neurol 1995;35:230-235
- ↵Trevisan CP, Carollo C, Segalla P, Angelini C, Drigo P, Giordano R. Congenital muscular dystrophy: brain alterations in an unselected series of Western patients. J Neurol Neurosurg Psychiatry 1991;54:330-334
- Aida N, Tamagawa K, Takada K, et al. Brain MRI in Fukuyama congenital muscular dystrophy. AJNR Am J Neuroradiol 1996;17:605-613
- ↵Mercuri E, Muntoni F, Berardinelli A, et al. Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status. Neuropediatrics 1995;26:3-7
- Reed UC, Marie SK, Vainzof M, et al. Congenital muscular dystrophy with cerebral white matter hypodensity: correlation of clinical features and merosin deficiency. Brain Dev 1996;18:53-58
- Nogen AG. Congenital muscle disease and abnormal findings on computerized tomography. Dev Med Child Neurol 1980;22:658-663
- Yoshioka M, Kuroki S, Mizue H. Congenital muscular dystrophy of non-Fukuyama type with characteristic CT images. Brain Dev 1987;9:316-318
- ↵Trevisan CP, Martinello F, Ferruzza E, Fanin M, Chevallay M, Tome FM. Brain alterations in the classical form of congenital muscular dystrophy: clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle. Childs Nerv Syst 1996;12:604-610
- ↵Engvall E, Davis GE, Dickerson K, Ruoslahti E, Varon S, Manthorpe M. Mapping of domains in human laminin using monoclonal antibodies: localization of the neurite-promoting site. J Cell Biol 1986;103:2457-2465
- Vuolteenaho R, Nissinen M, Sainio K, et al. Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues. J Cell Biol 1994;124:381-394
- ↵Pegoraro E, Mancias P, Swerdlow SH, et al. Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. Ann Neurol 1996;40:782-791
- Engvall E, Earwicker D, Day A, Muir D, Manthorpe M, Paulsson M. Merosin promotes cell attachment and neurite outgrowth and is a component of the neurite-promoting factor of RN22 schwannoma cells. Exp Cell Res 1992;198:115-123
- Tan E, Topaloglu H, Sewry C, et al. Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency. Neuromuscul Disord 1997;7:85-89
- ↵Villanova M, Malandrini A, Toti PE, et al. Localization of merosin in the normal human brain: implications for congenital muscular dystrophy with merosin deficiency. J Submicrosc Cytol Pathol 1996;28:1-4
- Leyten QH, Gabreels FJM, Renier WO, et al. White matter abnormalities in congenital muscular dystrophy. J Neurol Sci 1995;129:162-169
- ↵Hall JA. Neurodiagnosis: central nervous system. Handbook of Auditory Evoked Responses Boston: Allyn & Bacon; 1992;419-472
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MR Imaging Findings in Children with Merosin-Deficient Congenital Muscular Dystrophy
Pilar A. Caro, Mena Scavina, Eric Hoffman, Elena Pegoraro, Harold G. Marks
American Journal of Neuroradiology Feb 1999, 20 (2) 324-326;
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