HISTOPATHOLOGICAL LIVER FINDINGS IN PATIENTS WITH HEPATOCEREBRAL MITOCHONDRIAL DEPLETION SYNDROME WITH DEFINED MOLECULAR BASIS

被引:0
|
作者
Pronicki, Maciej [1 ]
Piekutowska-Abramczuk, Dorota [2 ]
Rokicki, Dariusz [3 ]
Iwanicka-Pronicka, Katarzyna [2 ,4 ]
Grajkowska, Wieslawa [1 ]
机构
[1] Childrens Mem Hlth Inst, Dept Pathol, Aleja Dzieci Polskich 20, PL-04730 Warsaw, Poland
[2] Childrens Mem Hlth Inst, Dept Genet, Warsaw, Poland
[3] Childrens Mem Hlth Inst, Dept Pediat Nutr & Metab Disorders, Warsaw, Poland
[4] Childrens Mem Hlth Inst, Dept Audiol & Phoniatr, Warsaw, Poland
关键词
catechins; epigallocatechin-3-gallate; EGCG; obesity; fatty liver;
D O I
10.5114/PJP.2019.90401
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
引用
收藏
页码:224 / 225
页数:2
相关论文
共 50 条
  • [21] CLINICAL, BIOCHEMICAL AND MORPHOLOGICAL FEATURES OF HEPATOCEREBRAL SYNDROME WITH MITOCHONDRIAL DNA DEPLETION DUE TO DEOXYGUANOSINE KINASE DEFICIENCY
    Labarthe, F.
    Dobbelaere, D.
    Devisme, L.
    De Muret, A.
    Jardel, C.
    Taanman, J-W
    Gottrand, F.
    Lonmbes, A.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 : 128 - 128
  • [22] Mitochondrial DNA depletion syndrome causing liver failure
    Sunita Bijarnia-Mahay
    Neelam Mohan
    Deepak Goyal
    I. C. Verma
    K. E. Elizabeth
    K. Jubin
    Indian Pediatrics, 2014, 51 : 666 - 668
  • [23] Liver Pathology in Infantile Mitochondrial DNA Depletion Syndrome
    Hazard, Florette K.
    Ficicioglu, Can H.
    Ganesh, Jaya
    Ruchelli, Eduardo D.
    PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2013, 16 (06) : 415 - 424
  • [24] Mitochondrial DNA depletion syndrome causing liver failure
    Bijarnia-Mahay, Sunita
    Mohan, Neelam
    Goyal, Deepak
    Verma, I. C.
    INDIAN PEDIATRICS, 2014, 51 (08) : 666 - 668
  • [25] Maternal uniparental disomy of chromosome 2 in a patient with a DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome
    Haudry, Coralie
    de Lonlay, Pascale
    Malan, Valerie
    Bole-Feysot, Christine
    Assouline, Zahra
    Pruvost, Solenn
    Brassier, Anais
    Bonnefont, Jean-Paul
    Munnich, Arnold
    Roetig, Agnes
    Lebre, Anne-Sophie
    MOLECULAR GENETICS AND METABOLISM, 2012, 107 (04) : 700 - 704
  • [26] Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure
    Al-Hussaini, Abdulrahman
    Faqeih, Eissa
    El-Hattab, Ayman W.
    Alfadhel, Majid
    Asery, Ali
    Alsaleem, Badr
    Bakhsh, Eman
    Ali, Ashraf
    Alasmari, Ali
    Lone, Khurram
    Nahari, Ahmed
    Eyaid, Wafaa
    Al Balwi, Mohammed
    Craig, Kate
    Butterworth, Anna
    He, Langping
    Taylor, Robert W.
    JOURNAL OF PEDIATRICS, 2014, 164 (03): : 553 - +
  • [27] MPV17 hepatocerebral mitochondrial DNA depletion syndrome presenting as acute flaccid paralysis - A case report
    Pyal, Anjan
    Paramasivam, Arumugam
    Meena, Angamuthu Kannan
    Bhavana, Velpula Bhagya
    Thangaraj, Kumarasamy
    MITOCHONDRION, 2017, 37 : 41 - 45
  • [28] Molecular genetic diagnosis of mitochondrial DNA depletion syndrome and Alpers syndrome
    Fratter, Carl
    O'Rourke, A.
    Marchington, D.
    Morten, K.
    Seller, A.
    Poulton, J.
    JOURNAL OF MEDICAL GENETICS, 2006, 43 : S80 - S80
  • [29] MITOCHONDRIAL DNA DEPLETION SYNDROME IN A NEONATE WITH FATAL LIVER FAILURE
    van der Meer, S. B.
    Jacobs, L.
    Rubio-Gozalbo, M. E.
    Bakker, J. A.
    Spaapen, L. J. M.
    Smeets, H. J. M.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 : 127 - 127
  • [30] Conjugated hyperbilirubinemia in infancy (mitochondrial DNA depletion syndrome, liver)
    Dimmick, J
    PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2004, 7 (06) : 625 - 628