Unusual ribbon-like periventricular heterotopia with congenital cataracts in a Japanese girl

被引:1
|
作者
Tsuburaya, Rie
Uematsu, Mitsugu [1 ]
Kikuchi, Atsuo
Hino-Fukuyo, Naomi
Kunishima, Shinji [2 ]
Kato, Mitsuhiro [3 ]
Haginoya, Kazuhiro [4 ]
Tsuchiya, Shigeru
机构
[1] Tohoku Univ, Dept Pediat, Sch Med, Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Natl Hosp Org, Nagoya Med Ctr, Clin Res Ctr, Dept Adv Diag, Nagoya, Aichi, Japan
[3] Yamagata Univ, Fac Med, Dept Pediat, Yamagata 990, Japan
[4] Takuto Rehabil Ctr Children, Dept Pediat Neurol, Sendai, Miyagi, Japan
关键词
ribbon-like periventricular heterotopia; migration disorders; congenital cataract; West syndrome;
D O I
10.1002/ajmg.a.34258
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Periventricular heterotopia (PH), clumps of neurons mislocated beside the ventricle, is caused by failure to initiate migration during embryogenesis. We report on a 32-month-old Japanese girl with a unique subtype of PH, namely ribbon-like PH. The patient presented with severe psychomotor developmental delay, intractable epilepsy, and congenital cataracts and developed West syndrome phenotype. Brain magnetic resonance imaging revealed a unique undulating form of PH, categorized as ribbon-like PH, and other brain malformations including simplified gyri and dysgenesis of the corpus callosum. There was no evidence of prenatal TORCH infection or associated syndrome. Array-based comparative genomic hybridization revealed no chromosomal rearrangements. Genetic analyses of the FLNA, DCX, ARX, LIS1, and TUBA1A genes showed no mutations. Although little is known about ribbon-like PH, the clinical manifestations in our patient clearly differed from those in other reported patients. 2012 Wiley Periodicals, Inc.
引用
收藏
页码:674 / 677
页数:4
相关论文
共 5 条
  • [1] Megalencephaly, polymicrogyria and ribbon-like band heterotopia: A new cortical malformation
    Kobayashi, Yu
    Magara, Shinichi
    Okazaki, Kenichi
    Komatsubara, Takao
    Saitsu, Hirotomo
    Matsumoto, Naomichi
    Kato, Mitsuhiro
    Tohyama, Jun
    BRAIN & DEVELOPMENT, 2016, 38 (10): : 950 - 953
  • [2] EML1-associated brain overgrowth syndrome with ribbon-like heterotopia
    Oegema, Renske
    McGillivray, George
    Leventer, Richard
    Le Moing, Anne-Gaelle
    Bahi-Buisson, Nadia
    Barnicoat, Angela
    Mandelstam, Simone
    Francis, David
    Francis, Fiona
    Mancini, Grazia M. S.
    Savelberg, Sanne
    van Haaften, Gijs
    Mankad, Kshitij
    Lequin, Maarten H.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2019, 181 (04) : 627 - 637
  • [3] A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects
    Markus, Fenja
    Kannengiesser, Annika
    Naeder, Patricia
    Atigbire, Paul
    Scholten, Alexander
    Voesing, Christine
    Bueltmann, Eva
    Korenke, G. Christoph
    Owczarek-Lipska, Marta
    Neidhardt, John
    JOURNAL OF HUMAN GENETICS, 2021, 66 (12) : 1159 - 1167
  • [4] A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects
    Fenja Markus
    Annika Kannengießer
    Patricia Näder
    Paul Atigbire
    Alexander Scholten
    Christine Vössing
    Eva Bültmann
    G. Christoph Korenke
    Marta Owczarek-Lipska
    John Neidhardt
    Journal of Human Genetics, 2021, 66 : 1159 - 1167
  • [5] [AEPH2][GeSb2S6]•CH3OH: a thiogermanate-thioantimonate featuring an infinite ribbon-like structure with an unusual {GeSb3S11} unit and exhibiting the ability of photocatalytic degradation of organic dye
    Feng, Mei-Ling
    Hu, Chun-Li
    Wang, Kai-Yao
    Du, Cheng-Feng
    Huang, Xiao-Ying
    CRYSTENGCOMM, 2013, 15 (25): : 5007 - 5011