Preimplantation genetic diagnosis of human leukocyte antigen for X-linked immunoproliferative syndrome caused by SAP mutation

被引：1
|
作者：
Lukaszuk, Krzysztof [1 ,2 ,3 ]
Kalwak, Krzysztof [4 ]
Pukszta, Sebastian [1 ]
Liss, Joanna [1 ]
Jakiel, Grzegorz [5 ]
Woclawek-Potocka, Izabela [6 ]
Galvao, Antonio [6 ]
Wasniewski, Tomasz [3 ]
机构：
[1] INVICTA Fertil & Reprod Ctr, Gdansk, Poland
[2] Med Univ, Dept Nursing, Gdansk, Poland
[3] Warmia & Masuria Univ, Dept Gynecol & Obstet, Olsztyn, Poland
[4] Wroclaw Med Univ, Fac Med, Dept Pediat Hematol Oncol & Bone Marrow Transplan, Warsaw, Poland
[5] Med Ctr Postgrad Educ, Dept Obstet & Gynaecol, Warsaw, Poland
[6] Polish Acad Sci, Inst Anim Reprod & Food Res, Dept Reprod Immunol & Pathol, Olsztyn, Poland
来源：
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY | 2014年 / 182卷
关键词：
Preimplantation genetic diagnosis (PGD); IVF; X-linked immunoproliferative syndrome (XLP); SAP mutation; HLA typing;
D O I：
10.1016/j.ejogrb.2014.09.034
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
引用
收藏
页码：248 / 249
页数：2
相关论文
共 50 条
  • [21] X-linked Dysgammaglobulinemia Caused by Hypomorphic XIAP Mutation
    Nishida, N.
    Yang, X.
    Kanegane, H.
    Sanayama, K.
    Goi, K.
    Sugita, K.
    Kato, K.
    Miyawaki, T.
    PROCEEDINGS OF THE 15TH MEETING OF THE EUROPEAN SOCIETY IMMUNODEFICIENCIES (ESID), 2013, : 57 - 60
  • [22] Normal twins born following preimplantation genetic diagnosis in a couple affected by X-linked hydrocephaly
    Drury, KC
    Schalue, TK
    Pitcher, GF
    Kipersztok, S
    Williams, RS
    Konicek, JR
    JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 1996, 13 (10) : 797 - 800
  • [23] X-LINKED DYSGAMMGLOBULINEMIA CAUSED BY HYPOMORPHIC XIAP MUTATION
    Nishida, N.
    Yang, X.
    Kanegane, H.
    Sanayama, K.
    Goi, K.
    Sugita, K.
    Kato, K.
    Miyawaki, T.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2012, 32 : 52 - 53
  • [24] Preimplantation genetic diagnosis (PGD) for couples at risk of X-linked disease and for balanced translocation carriers
    Weremowicz, S
    Racowsky, C
    Sandstrom, DJ
    Nureddin, A
    Jackson, KV
    Wilkins-Haug, LE
    Morton, CC
    Miron, PM
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 596 - 596
  • [25] X-linked ectodermal dysplasia with immunodeficiency caused by NEMO mutation - Early recognition and diagnosis
    Mancini, Anthony J.
    Lawley, Leslie P.
    Uzel, Gulbu
    ARCHIVES OF DERMATOLOGY, 2008, 144 (03) : 342 - 346
  • [26] The future (R)evolution of preimplantation genetic Diagnosis/Human leukocyte antigen testing: Ethical reflections
    de Wert, Guido
    Liebaers, Inge
    Van De Velde, Hilde
    STEM CELLS, 2007, 25 (09) : 2167 - 2172
  • [27] Attitudes toward genetic diagnosis and prenatal diagnosis of X-linked Alport syndrome in China
    Zhang, Hongwen
    Ding, Jie
    Wang, Fang
    Yu, Lixia
    NEPHROLOGY, 2012, 17 (04) : 398 - 401
  • [28] Polar body based preimplantation diagnosis for X-linked disorders.
    Verlinsky, Y
    Rechitsky, S
    Verlinsky, O
    Kenigsberg, D
    Moshella, J
    Ivakhnenko, V
    Masciangelo, C
    Strom, C
    Kuliev, A
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 666 - 666
  • [29] Preimplantation genetic diagnosis of X-linked Charcot-Marie-Tooth disease by indirect linkage analysis
    Borgulova, Irena
    Putzova, Martina
    Soldatova, Inna
    Stejskal, David
    MEDICINA CLINICA, 2018, 150 (06): : 215 - 219
  • [30] Barth Syndrome: An X-linked Cardiomyopathy with a Novel Mutation
    Aljishi, Emtethal
    Ali, Fouad
    INDIAN JOURNAL OF PEDIATRICS, 2010, 77 (12): : 1432 - 1433
12345