Paternally inherited case of congenital DM1: Brain MRI and review of literature

被引:9
作者
Di Costanzo, Alfonso [1 ]
de Cristofaro, Mario [2 ]
Di Iorio, Giuseppe [2 ]
Daniele, Aurora [1 ]
Bonavita, Simona [2 ]
Tedeschi, Gioacchino [2 ]
机构
[1] Univ Molise, Dept Hlth Sci, I-86100 Campobasso, Italy
[2] Univ Naples 2, Dept Neurol Sci, I-80138 Naples, Italy
关键词
Myotonic dystrophy; Paternal inheritance; Magnetic resonance imaging; Brain; MYOTONIC-DYSTROPHY TYPE-1; TRANSMISSION; FORM;
D O I
10.1016/j.braindev.2008.04.008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The congenital form of myotonic dystrophy type I (CDMI) has ail almost exclusively maternal transmission and is characterized by mental retardation and by moderate/severe ventriculomegaly and white matter hyperintensities on brain magnetic resonance imaging (MRI). We report a 20-year-old case of CDM1 with paternal inheritance showing mental retardation and normal brain MRI, and presenting at birth with hypotonia, facial weakness and feeding difficulties. We reviewed the literature for studies addressing the brain neuroimaging in paternally transmitted CDM1 and found four Studies reporting diffuse cerebral, frontal lobe or mild parietal cortical atrophy, or mild ventricular dilatation, without white matter abnormalities. To our knowledge, this is the first report describing normal brain MRI in a mentally retarded CDM1 patient with paternal transmission. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 82
页数:4
相关论文
共 11 条
[1]   PATERNAL TRANSMISSION OF CONGENITAL MYOTONIC-DYSTROPHY [J].
BERGOFFEN, J ;
KANT, J ;
SLADKY, J ;
MCDONALDMCGINN, D ;
ZACKAI, EH ;
FISCHBECK, KH .
JOURNAL OF MEDICAL GENETICS, 1994, 31 (07) :518-520
[2]   Brain MRI features of congenital- and adult-form myotonic dystrophy type 1: case-control study [J].
Di Costanzo, A ;
Di Salle, F ;
Santoro, L ;
Bonavita, V ;
Tedeschi, G .
NEUROMUSCULAR DISORDERS, 2002, 12 (05) :476-483
[3]   Myotonic dystrophy type I in childhood Long-term evolution in patients surviving the neonatal period [J].
Echenne, Bernard ;
Rideau, Aline ;
Roubertie, Agathe ;
Sebire, Guillaume ;
Rivier, Francois ;
Lemieux, Bernard .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2008, 12 (03) :210-223
[4]  
Harper P.S. Monckton., 2001, MYOTONIC DYSTROPHY, V3e
[5]   Congenital myotonic dystrophy pathology and somatic mosaicism [J].
Joseph, JT ;
Richards, CS ;
Anthony, DC ;
Upton, M ;
PerezAtayde, AR ;
Greenstein, P .
NEUROLOGY, 1997, 49 (05) :1457-1460
[6]   Brain magnetic resonance image changes in a family with congenital and classic myotonic dystrophy [J].
Kuo, HC ;
Hsiao, KM ;
Chen, CJ ;
Hsieh, YC ;
Huang, CC .
BRAIN & DEVELOPMENT, 2005, 27 (04) :291-296
[7]   Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophy [J].
Martinello, F ;
Piazza, A ;
Pastorello, E ;
Angelini, C ;
Trevisan, CP .
JOURNAL OF NEUROLOGY, 1999, 246 (03) :186-192
[8]   Cerebral involvement in myotonic dystrophies [J].
Meola, Giovanni ;
Sansone, Valeria .
MUSCLE & NERVE, 2007, 36 (03) :294-306
[9]   A CASE OF PATERNALLY INHERITED CONGENITAL MYOTONIC-DYSTROPHY [J].
NAKAGAWA, M ;
YAMADA, H ;
HIGUCHI, I ;
KAMINISHI, Y ;
MIKI, T ;
JOHNSON, K ;
OSAME, M .
JOURNAL OF MEDICAL GENETICS, 1994, 31 (05) :397-400
[10]   Congenital myotonic dystrophy: report of paternal transmission [J].
Tanaka, Y ;
Suzuki, Y ;
Shimozawa, N ;
Nanba, E ;
Kondo, N .
BRAIN & DEVELOPMENT, 2000, 22 (02) :132-134