Os odontoideum in wolcott-rallison syndrome: a case series of 4 patients

被引:0
|
作者
R. P. Dias
C. R. Buchanan
N. Thomas
S. Lim
G. Solanki
SEJ Connor
T. G. Barrett
R. R. Kapoor
机构
[1] Birmingham Children’s Hospital,Department of Paediatric Endocrinology and Diabetes
[2] King’s College Hospital,Department of Child Health
[3] Kings College Hospital,Department of Neurosurgery
[4] St John’s Hospital,Department of Paediatrics
[5] Birmingham Children’s Hospital,Department of Neurosurgery
[6] Kings College Hospital,Department of Neuroradiology
[7] University of Birmingham,Centre for Rare Diseases and Personalized Medicine, Institute of Biomedical Research (West), School of Clinical and Experimental Medicine
关键词
Neonatal Diabetes; Os Odontoideum; Wolcott-Rallison Syndrome; Atlanto-axial instability;
D O I
暂无
中图分类号
学科分类号
摘要
Wolcott-Rallison Syndrome is the commonest cause of neonatal diabetes in consanguineous families. It is associated with liver dysfunction, epiphyseal dysplasia, and developmental delay. It is caused by mutations in eukaryotic translation initiation factor 2-α kinase 3 (EIF2AK3).
引用
下载
收藏
相关论文
共 50 条
  • [31] Frequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review
    Habeb, Abdelhadi M.
    LIBYAN JOURNAL OF MEDICINE, 2013, 8
  • [32] Organisation of the human PAX4 gene and its exclusion as a candidate for the Wolcott-Rallison syndrome
    Bonthron, DT
    Dunlop, N
    Barr, DGD
    El Sanousi, AA
    Al-Gazali, LI
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (04) : 288 - 292
  • [33] Wolcott-Rallison Syndrome-Endocrinopathy with Recurrent Acute Liver Failure
    Joseph J. Valamparampil
    Naresh Shanmugam
    Mohamed Rela
    Indian Pediatrics, 2019, 56 : 1055 - 1056
  • [34] Wolcott-Rallison Syndrome With Different Clinical Presentations and Genetic Patterns in 2 Infants
    Davoodi, Mohamad Ahangar
    Karamizadeh, Zohreh
    Ghobadi, Fatemeh
    Shokrpour, Nasrin
    HEALTH CARE MANAGER, 2018, 37 (04) : 354 - 357
  • [35] Practical management in Wolcott-Rallison syndrome with associated hypothyroidism, neutropenia, and recurrent liver failure: A case report
    Lundgren, Markus
    De Franco, Elisa
    Arnell, Henrik
    Fischler, Bjoern
    CLINICAL CASE REPORTS, 2019, 7 (06): : 1133 - 1138
  • [36] Novel mutation in the ElF2AK3 gene in a case of Wolcott-Rallison syndrome.
    Biason-Lauber, A
    Lang-Muritano, M
    Schoenle, EJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 615 - 615
  • [37] Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation
    Gurbuz, Fatih
    Yuksel, Bilgin
    Topaloglu, Ali Kemal
    JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2016, 8 (04) : 496 - 497
  • [38] Diabetes management in Wolcott-Rallison syndrome: analysis from the German/Austrian DPV database
    Alena Welters
    Thomas Meissner
    Katja Konrad
    Clemens Freiberg
    Katharina Warncke
    Sylvia Judmaier
    Olga Kordonouri
    Michael Wurm
    Matthias Papsch
    Gisela Fitzke
    Silke Christina Schmidt
    Sascha R. Tittel
    Reinhard W. Holl
    Orphanet Journal of Rare Diseases, 15
  • [39] Long-term follow-up of a child with Wolcott-Rallison syndrome
    Shah, Nikhil
    Karguppikar, Madhura Bharat
    Khadilkar, Vaman
    Khadilkar, Anuradha
    BMJ CASE REPORTS, 2021, 14 (05)
  • [40] First European Case of Simultaneous Liver and Pancreas Transplantation as Treatment of Wolcott-Rallison Syndrome in a Small Child
    Nordstrom, Johan
    Lundgren, Markus
    Jorns, Carl
    Fischler, Bjorn
    Arnell, Henrik
    Dlugosz, Rafal
    Sandberg, John
    Wennberg, Lars
    Nowak, Greg
    TRANSPLANTATION, 2020, 104 (03) : 522 - 525