Unrelated cord blood transplantation in a girl with Hoyeraal-Hreidarsson syndrome

被引：10

作者：

Coman, D. ^{[1
]}

Herbert, A. R. ^{[2
]}

McGill, J. ^{[1
,3
]}

Lockwood, L. ^{[2
]}

Hallahan, A. R. ^{[2
]}

机构：

[1] Univ Queensland, Royal Childrens Hosp, Dept Metab Med, Brisbane, Qld, Australia

[2] Univ Queensland, Royal Childrens Hosp, Dept Haematol & Oncol, Brisbane, Qld, Australia

[3] Univ Queensland, Royal Childrens Hosp, Dept Chem Pathol, Brisbane, Qld, Australia

来源：

BONE MARROW TRANSPLANTATION | 2008年 / 42卷 / 04期

关键词：

D O I：

10.1038/bmt.2008.163

中图分类号：

Q6 [生物物理学];

学科分类号：

071011 ;

摘要：

[No abstract available]

引用

页码：293 / 294

页数：2

共 11 条

[1]

AALFS CM, 1995, EUR J PEDIATR, V154, P304, DOI 10.1007/BF01957367

[2] A case of Hoyeraal-Hreidarsson syndrome: Delayed myelination and hypoplasia of corpus callosum are other important signs [J].

Akaboshi, S ;

Yoshimura, M ;

Hara, T ;

Kageyama, H ;

Nishikwa, K ;

Kawakami, T ;

Ieshima, A ;

Takeshita, K .

NEUROPEDIATRICS, 2000, 31 (03) :141-144

[3] Rapid and complete donor chimerism in adult recipients of unrelated donor umbilical cord blood transplantation after reduced-intensity conditioning [J].

Barker, JN ;

Weisdorf, DJ ;

DeFor, TE ;

Blazar, BR ;

Miller, JS ;

Wagner, JE .

BLOOD, 2003, 102 (05) :1915-1919

[4] High incidence of cytomegalovirus infection after nonmyeloablative stem cell transplantation: potential role of Campath-1H in delaying immune reconstitution [J].

Chakrabarti, S ;

Mackinnon, S ;

Chopra, R ;

Kottaridis, PD ;

Peggs, K ;

O'Gorman, P ;

Chakraverty, R ;

Marshall, T ;

Osman, H ;

Mahendra, P ;

Craddock, C ;

Waldmann, H ;

Hale, G ;

Fegan, CD ;

Yong, K ;

Goldstone, AH ;

Linch, DC ;

Milligan, DW .

BLOOD, 2002, 99 (12) :4357-4363

[5] A novel DKC1 mutation, severe combined immunodeficiency (T+B-NK-SCID) and bone marrow transplantation in an infant with Hoyeraal-Hreidarsson syndrome [J].

Cossu, F ;

Vulliamy, TJ ;

Marrone, A ;

Badiali, M ;

Cao, A ;

Dokal, I .

BRITISH JOURNAL OF HAEMATOLOGY, 2002, 119 (03) :765-768

[6] A SYNDROME OF PROGRESSIVE PANCYTOPENIA WITH MICROCEPHALY, CEREBELLAR HYPOPLASIA AND GROWTH FAILURE [J].

HREIDARSSON, S ;

KRISTJANSSON, K ;

JOHANNESSON, G ;

JOHANNSSON, JH .

ACTA PAEDIATRICA SCANDINAVICA, 1988, 77 (05) :773-775

[7] Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1 [J].

Knight, SW ;

Heiss, NS ;

Vulliamy, TJ ;

Aalfs, CM ;

McMahon, C ;

Richmond, P ;

Jones, A ;

Hennekam, RCM ;

Poustka, A ;

Mason, PJ ;

Dokal, I .

BRITISH JOURNAL OF HAEMATOLOGY, 1999, 107 (02) :335-339

[8] Sensitivity to radiation and alkylating agent of peripheral lymphocytes and fibroblasts in a Hoyeraal-Hreidarsson syndrome patient [J].

M'kacher, R ;

Laithier, V ;

Valent, A ;

Delhommeau, F ;

Violot, D ;

Deutsch, E ;

Dossou, J ;

Béron-Gaillard, N ;

Girinsky, T ;

Bourhis, J ;

Carde, P ;

Bernheim, A ;

Parmentier, C .

PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2003, 20 (08) :651-656

[9] Familial cerebellar hypoplasia and pancytopenia without chromosomal breakages [J].

Mahmood, F ;

King, MD ;

Smyth, OP ;

Farrell, MA .

NEUROPEDIATRICS, 1998, 29 (06) :302-306

[10]

Ozdemir Mehmet Akif, 2004, Haematologica, V89, pECR38

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