A FAMILY WITH HEREDITARY ANKYLOGLOSSIA COMPLICATED BY HETEROCHROMIA IRIDES AND A CONGENITAL CLASPED THUMB

被引：3
|
作者：
SATO, T
IIDA, M
YAMAGUCHI, Y
机构：
来源：
INTERNATIONAL JOURNAL OF ORAL SURGERY | 1983年 / 12卷 / 05期
关键词：
D O I：
10.1016/S0300-9785(83)80027-1
中图分类号：
R78 [口腔科学];
学科分类号：
1003 ;
摘要：
引用
收藏
页码：359 / 362
页数：4
相关论文
共 50 条
  • [31] HEREDITARY SPASTIC ATAXIA WITH CONGENITAL MIOSIS - 4 CASES IN ONE FAMILY
    DICK, DJ
    NEWMAN, PK
    CLELAND, PG
    BRITISH JOURNAL OF OPHTHALMOLOGY, 1983, 67 (02) : 97 - 101
  • [32] Complicated Hereditary Spastic Paraplegia Caused by SERAC1 Variants in a Chinese Family
    Yan, Dandan
    Chen, Shaopei
    Cai, Fengying
    Shu, Jianbo
    Zhi, Xiufang
    Zheng, Jie
    Zhang, Chunhua
    Li, Dong
    Cai, Chunquan
    FRONTIERS IN PEDIATRICS, 2022, 9
  • [33] A family of Phospholipase A2-associated neurodegeneration presented as complicated hereditary spastic paraplegia
    Wu, M. C.
    Lan, M. Y.
    Li, J. W.
    Chen, Y. F.
    Chang, Y. Y.
    MOVEMENT DISORDERS, 2019, 34 : S200 - S200
  • [34] STUDIES USING HUMAN LENSES FROM A FAMILY DISPLAYING HEREDITARY CONGENITAL CATARACTS
    RUSSELL, P
    UGA, S
    ZIGLER, JS
    KAISERKUPFER, M
    KUWABARA, T
    VISION RESEARCH, 1981, 21 (01) : 169 - 172
  • [35] Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia
    Kancheva, Dahlia
    Chamova, Teodora
    Guergueltcheva, Velina
    Mitev, Vanio
    Azmanov, Dimitar N.
    Kalaydjieva, Luba
    Tournev, Ivailo
    Jordanova, Albena
    MOVEMENT DISORDERS, 2015, 30 (06) : 854 - 858
  • [36] A Novel Mutation of the Decorin Gene Identified in a Korean Family With Congenital Hereditary Stromal Dystrophy
    Kim, Jae-hyung
    Ko, Jung Min
    Lee, Inchul
    Kim, Jae Yong
    Kim, Myoung Joon
    Tchah, Hungwon
    CORNEA, 2011, 30 (12) : 1473 - 1477
  • [37] Novel Type of Complicated Autosomal Dominant Hereditary Spastic Paraplegia Associated with Congenital Distal Arthrogryposis Type I
    Hedera, Peter
    Moretti, Paolo
    Howard, Jane
    Zhao, Jiali
    BRAIN SCIENCES, 2018, 8 (07)
  • [38] Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family
    Mitsuko Nakashima
    Motoi Nakano
    Akiyoshi Hirano
    Tatsuya Kishino
    Shinji Kondoh
    Nobutomo Miwa
    Norio Niikawa
    Koh-ichiro Yoshiura
    Journal of Human Genetics, 2008, 53 : 34 - 41
  • [39] A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis
    Sahin, Yavuz
    Gungor, Olcay
    Ayaz, Akif
    Gungor, Gulay
    Sahin, Bedia
    Yaykasli, Kursad
    Ceylaner, Serdar
    BRAIN & DEVELOPMENT, 2017, 39 (02): : 166 - 170
  • [40] Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family
    Nakashima, Mitsuko
    Nakano, Motoi
    Hirano, Akiyoshi
    Kishino, Tatsuya
    Kondoh, Shinji
    Miwa, Nobutomo
    Niikawa, Norio
    Yoshiura, Koh-ichiro
    JOURNAL OF HUMAN GENETICS, 2008, 53 (01) : 34 - 41
12345