Somatic and germ line mosaicism and mutation origin for a mutation in the L1 gene in a family with X-linked hydrocephalus

被引:0
|
作者
Du, JS
Bason, L
Woffendin, H
Zackai, E
Kenwrick, S
机构
[1] Univ Cambridge, Dept Med, Addenbrookes Hosp, Cambridge CB2 2QQ, England
[2] Childrens Hosp Philadelphia, Clin Genet Ctr, Philadelphia, PA 19104 USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1998年 / 75卷 / 02期
基金
英国惠康基金;
关键词
X-linked hydrocephalus; L1; L1CAM; neural cell adhesion molecules; somatic mosaicism;
D O I
10.1002/(SICI)1096-8628(19980113)75:2<200::AID-AJMG16>3.0.CO;2-T
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
X-linked hydrocephalus is caused by mutations in the gene for neural cell adhesion molecule L1 (L1CAM), In this report, we describe identification of a mutation in an isolated case of hydrocephalus with adducted thumbs, Tracing the origin of the mutation within the family showed a degree of somatic mosaicism in the asymptomatic maternal grandfather of the propositus. This report highlights the need to take mosaicism into account when counselling relatives of affected individuals, (C) 1998 Wiley-Liss, Inc.
引用
收藏
页码:200 / 202
页数:3
相关论文
共 50 条
  • [1] X-linked hydrocephalus:: Another two families with an L1 mutation
    Criado, GR
    Aytés, AP
    Martínez, F
    Vos, YJ
    Verlind, E
    López, AGM
    Sánchez, IGD
    Schrander-Stumpel, C
    GENETIC COUNSELING, 2003, 14 (01): : 57 - 65
  • [2] A new mutation of the L1CAM gene in an X-linked hydrocephalus family
    Izumoto, S
    Yamasaki, M
    Arita, N
    Hiraga, S
    Ohnishi, T
    Fujitani, K
    Sakoda, S
    Hayakawa, T
    CHILDS NERVOUS SYSTEM, 1996, 12 (12) : 742 - 747
  • [3] A MISSENSE MUTATION CONFIRMS THE L1 DEFECT IN X-LINKED HYDROCEPHALUS (HSAS)
    JOUET, M
    ROSENTHAL, A
    MACFARLANE, J
    KENWRICK, S
    DONNAI, D
    NATURE GENETICS, 1993, 4 (04) : 331 - 331
  • [4] Prenatal diagnosis of X-linked hydrocephalus in a family with a novel mutation in L1CAM gene
    Ochando, I.
    Vidal, V.
    Gascon, J.
    Acien, M.
    Urbano, A.
    Rueda, J.
    JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2016, 36 (03) : 403 - 405
  • [5] X-linked hydrocephalus:: A novel missense mutation in the L1CAM gene
    Sztriha, L
    Vos, YJ
    Verlind, E
    Johansen, J
    Berg, B
    PEDIATRIC NEUROLOGY, 2002, 27 (04) : 293 - 296
  • [6] Discordant segregation of Xq28 markers and a mutation in the L1 gene in a family with X linked hydrocephalus
    Jouet, M
    Strain, L
    Bonthron, D
    Kenwrick, S
    JOURNAL OF MEDICAL GENETICS, 1996, 33 (03) : 248 - 250
  • [7] A novel mutation in L1CAM gene in a Japanese patient with X-linked hydrocephalus
    Okamoto, N
    Wada, Y
    Kawabata, H
    Ishikiriyama, S
    Takahashi, S
    JAPANESE JOURNAL OF HUMAN GENETICS, 1996, 41 (04): : 431 - 437
  • [8] L1CAM mutation in a Japanese family with X-linked hydrocephalus: a study for genetic counseling
    Takahashi, S
    Makita, Y
    Okamoto, N
    Miyamoto, A
    Oki, J
    BRAIN & DEVELOPMENT, 1997, 19 (08): : 559 - 562
  • [9] MUTATIONS IN THE L1 LOCUS IN X-LINKED HYDROCEPHALUS
    JOUET, M
    ROSENTHAL, A
    KENWRICK, S
    CYTOGENETICS AND CELL GENETICS, 1993, 64 (3-4): : 179 - 180
  • [10] A novel nonsense mutation in the L1CAM gene responsible for X-linked congenital hydrocephalus
    Guo, Dewei
    Shi, Yuting
    Jian, Wenyan
    Fu, Yimei
    Yang, Hui
    Guo, Manhui
    Yong, Wenjing
    Chen, Gang
    Deng, Huan
    Qin, Yan
    Liao, Weihua
    Yao, Ruojin
    JOURNAL OF GENE MEDICINE, 2020, 22 (07):