Moyamoya syndrome secondary to hereditary spherocytosis: A case report

被引:0
|
作者
Sun, Yidi [1 ]
Wang, Yaoyao [1 ]
Lian, Yajun [1 ]
Cheng, Xuan [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China
关键词
DISEASE;
D O I
10.1016/j.asjsur.2024.05.089
中图分类号
R61 [外科手术学];
学科分类号
摘要
引用
收藏
页码:4241 / 4242
页数:2
相关论文
共 50 条
  • [21] ACUTE RENAL FAILURE IN HEREDITARY SPHEROCYTOSIS - REPORT OF A CASE
    GRAHLMADSEN, R
    PALLISGA.G
    SCANDINAVIAN JOURNAL OF HAEMATOLOGY, 1968, 5 (01): : 41 - +
  • [22] CONCERNS OF A TEENAGER WITH HOMOZYGOUS HEREDITARY SPHEROCYTOSIS: CASE REPORT
    Araujo, C.
    Silva, R.
    Leite, V.
    Cartaxo, T.
    Furet, A.
    EUROPEAN PSYCHIATRY, 2014, 29
  • [23] Hereditary spherocytosis in a young male Report of an unusual case
    Kanellopoulou, T.
    Kontopidou, F. N.
    Dourakis, S. P.
    ARCHIVES OF HELLENIC MEDICINE, 2011, 28 (06): : 814 - 818
  • [24] NEPHROTIC SYNDROME AND HEREDITARY SPHEROCYTOSIS
    GIMENEZLLORT, A
    CAMACHODIAZ, JA
    ESTELLAAGUADO, J
    GARCIAGARCIA, L
    ANALES ESPANOLES DE PEDIATRIA, 1978, 11 (8-9): : 629 - 632
  • [25] Severe jaundice due to coexistence of Dubin-Johnson syndrome and hereditary spherocytosis: A case report
    Korkmaz, Ugur
    Duman, Ali Erkan
    Koc, Deniz Ogutmen
    Gurbuz, Yesim
    Dindar, Gokhan
    Ensaroglu, Fatih
    Sener, Selcuk Yusuf
    Senturk, Omer
    Hulagu, Sadettin
    TURKISH JOURNAL OF GASTROENTEROLOGY, 2011, 22 (04): : 422 - 425
  • [26] The course and outcome of pregnancy in patient with concomitant Gilbert syndrome and hereditary spherocytosis: a unique case report
    Bapaveva, C.
    Terzic, M.
    Togyzbayeva, K.
    Bekenova, A.
    Terzic, S.
    CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY, 2019, 46 (02): : 320 - 322
  • [27] Moyamoya syndrome with spherocytosis: Effect of splenectomy on strokes
    Tokunaga, Y
    Ohga, S
    Suita, S
    Matsushima, T
    Hara, T
    PEDIATRIC NEUROLOGY, 2001, 25 (01) : 75 - 77
  • [28] Outcome of a pregnancy in a patient with Moyamoya syndrome and secondary recurrent miscarriages - a case report
    Bohlmann, MK
    Fischer, R
    von Tengg-Kobligk, H
    Strowitzki, T
    Hendrik, HJ
    GEBURTSHILFE UND FRAUENHEILKUNDE, 2005, 65 (01) : 87 - 90
  • [29] New mutation in the β-spectrin gene in hereditary spherocytosis: A case report
    Jin, Changyu
    Hu, Huijie
    Li, Qingqing
    Lai, Yanli
    Wang, Jiaping
    Mu, Qitian
    Ouyang, Guifang
    Sheng, Lixia
    GENE REPORTS, 2024, 37
  • [30] Extramedullary Hematopoiesis in Hereditary Spherocytosis Deficient in Ankyrin: A Case Report
    E. Granjo
    R. Bauerle
    R. Sampaio
    P. Manata
    N. Torres
    A. Quintanilha
    International Journal of Hematology, 2002, 76 : 153 - 156