DOCK8 Large Genomic Deletions and Abdominal Vasculitis in Children with Autosomal Recessive hyper-IgE Syndrome

被引：0

作者：

Lugo Reyes, Saul Oswaldo ^{[1
]}

Okada, Satoshi ^{[2
]}

Antonio Yamazaki-Nakashimada, Marco ^{[3
]}

Prando, Carolina ^{[2
]}

Boisson-Dupuis, Stephanie ^{[2
]}

Casanova, Jean-Laurent ^{[2
]}

Picard, Capucine ^{[4
]}

机构：

[1] Natl Inst Pediat, Immunodeficiencies Res Unit, Mexico City, DF, Mexico

[2] Rockefeller Univ, St Giles Lab Human Genet Infect Dis, New York, NY 10021 USA

[3] Natl Inst Pediat, Dept Clin Immunol, Mexico City, DF, Mexico

[4] Univ Paris 05, Hop Necker Enfants Malad, Paris, France

来源：

JOURNAL OF CLINICAL IMMUNOLOGY | 2012年 / 32卷 / 02期

关键词：

D O I：

暂无

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

引用

页码：379 / 379

页数：1

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[32] Acute Viral Retinitis in a Patient with Autosomal Recessive Hyper-IGE Syndrome [J].

Bustamante Ogando, J. C. ;

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[33] Identification of genes mutated in autosomal-recessive hyper-IgE syndrome [J].

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CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2008, 154 :53-53

[34] Hypomorphic Mutation in DOCK8 Causes Combined Immune Deficiency Without Hyper-IGE [J].

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[35] Outcome of Allogeneic Hematopoietic stem cell transplantation in Autosomal Recessive Hyper IgE syndrome due to DOCK8 deficiency Single Center Experience [J].

Elshourbagi, S. A. ;

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[36] T CELL SUBSETS IN A MOUSE MODEL OF AUTOSOMAL RECESSIVE HYPER-IgE SYNDROME [J].

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[37] Gross generalized molluscum contagiosum in a patient with autosomal recessive hyper-IgE syndrome [J].

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BRITISH JOURNAL OF DERMATOLOGY, 2012, 166 (01) :E3-E4

[38] Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE [J].

Kienzler, Anne-Kathrin ;

van Schouwenburg, Pauline A. ;

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Marwah, Ishita ;

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CLINICAL IMMUNOLOGY, 2016, 163 :17-21

[39] Rare Case of Adult Onset DOCK8 Mutated Hyper Ige Syndrome [J].

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[40] Updated outcome of allogenic haematopoietic stem cell transplatation in autosomal recessive hyper-IgE syndrome due to dock 8 deficiency: Single center experience [J].

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BONE MARROW TRANSPLANTATION, 2017, 52 :S383-S383

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