MATERNALLY INHERITED LEIGH SYNDROME

被引:76
|
作者
CIAFALONI, E
SANTORELLI, FM
SHANSKE, S
DEONNA, T
ROULET, E
JANZER, C
PESCIA, G
DIMAURO, S
机构
[1] COLUMBIA PRESBYTERIAN MED CTR, H HOUSTON MERRITT CLIN RES CTR MUSCULAR DYSTROPHY, NEW YORK, NY 10032 USA
[2] CHU VAUDOIS, NEUROPEDIAT UNIT, CH-1011 LAUSANNE, SWITZERLAND
[3] CHU VAUDOIS, DIV AUTONOME GENET MED, CH-1011 LAUSANNE, SWITZERLAND
[4] UNIV LAUSANNE, INST PATHOL, DIV NEUROPATHOL, CH-1000 LAUSANNE 17, SWITZERLAND
来源
JOURNAL OF PEDIATRICS | 1993年 / 122卷 / 03期
关键词
D O I
10.1016/S0022-3476(05)83431-6
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
A 6 1/2-year-old girl had developmental regression, and Leigh syndrome was diagnosed. A second girl born to the some mother after heterologous artificial insemination also lost acquired skills and died of 2 1/2 years of age; neuropathologic examination confirmed the diagnosis of Leigh syndrome. Tissues from both children and from the mother had a point mutation at nucleotide 8993 in the adenosinetriphosphatase 6-gene of mitochondrial DNA. This family illustrates that Leigh syndrome con be transmitted by maternal inheritance.
引用
收藏
页码:419 / 422
页数:4
相关论文
共 50 条
  • [41] MATERNALLY INHERITED MITOCHONDRIAL MYOPATHY AND MYOCLONIC EPILEPSY
    ROSING, HS
    HOPKINS, LC
    WALLACE, DC
    EPSTEIN, CM
    WEIDENHEIM, K
    ANNALS OF NEUROLOGY, 1985, 17 (03) : 228 - 237
  • [42] Retinopathy associated with maternally inherited diabetes and deafness
    Suribhatla, Rhea
    de Silva, Samantha R.
    EYE, 2025, 39 (SUPPL1) : 110 - 111
  • [43] Molecular pathogenetic mechanism of maternally inherited deafness
    GUAN Min XinDivision and Program in Human Genetics and Center for Hearing and Deafaess ResearchCincinnati Childrens Hospital Medical Center and Department of Pediatrics Universityof Cincinnati College of Medicine Cincinnati Ohio USA
    中华耳科学杂志, 2003, (03) : 53 - 61
  • [44] Molecular pathogenetic mechanism of maternally inherited deafness
    Guan, MX
    MITOCHONDRIAL PATHOGENESIS: FROM GENES AND APOPTOSIS TO AGING AND DISEASE, 2004, 1011 : 259 - 271
  • [45] Mitochondrial mutations in maternally inherited hearing loss
    Mutai, Hideki
    Watabe, Takahisa
    Kosaki, Kenjiro
    Ogawa, Kaoru
    Matsunaga, Tatsuo
    BMC MEDICAL GENETICS, 2017, 18
  • [46] Genetic Counselling for Maternally Inherited Mitochondrial Disorders
    Joanna Poulton
    Josef Finsterer
    Patrick Yu-Wai-Man
    Molecular Diagnosis & Therapy, 2017, 21 : 419 - 429
  • [47] Maternally inherited diabetes and deafness: A multicenter study
    Guillausseau, PJ
    Massin, P
    Dubois-LaForgue, D
    Timsit, J
    Virally, M
    Gin, H
    Bertin, E
    Blickle, JF
    Bouhanick, B
    Cahen, J
    Caillat-Zucman, S
    Charpentier, G
    Chedin, P
    Derrien, C
    Ducluzeau, PH
    Grimaldi, A
    Guerci, B
    Kaloustian, E
    Murat, A
    Olivier, F
    Paques, M
    Paquis-Flucklinger, V
    Porokhov, B
    Samuel-Lajeunesse, J
    Vialettes, B
    ANNALS OF INTERNAL MEDICINE, 2001, 134 (09) : 721 - 728
  • [48] Mitochondrial Disorder: Maternally Inherited Diabetes and Deafness
    Tsang, Stephen H.
    Aycinena, Alicia R. P.
    Sharma, Tarun
    ATLAS OF INHERITED RETINAL DISEASES, 2018, 1085 : 163 - 165
  • [49] Reply to Letter to the Editor "Maternally inherited diabetes and deafness is a mitochondrial multiorgan disorder syndrome (MIMODS)"
    Ko, Tzu-Hsiang
    Lee, Hsun-Hua
    Hsieh, An-Tsz
    Hu, Chaur-Jong
    Chen, Chih-Chung
    ACTA DIABETOLOGICA, 2017, 54 (10) : 981 - 982
  • [50] Accelerated cardiomyopathy in maternally inherited diabetes and deafness
    Mangiafico, RA
    Zeviani, M
    Bartoloni, G
    Fiore, CE
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY RESEARCH, 2004, 24 (01) : 15 - 21