Refractory autoimmune hemolytic anemia in a patient with chromosome 22q11.2 deletion syndrome

被引：8

作者：

Sakamoto, O

Imaizumi, M

Suzuki, A

Sato, A

Tanaka, T

Ogawa, E

Kumaki, S

Iinuma, K

机构：

[1] Tohoku Univ, Sch Med, Dept Pediat, Aoba Ku, Sendai, Miyagi 9808574, Japan

[2] Tohoku Univ, Sch Med, Dept Pediat Hematol & Oncol, Sendai, Miyagi 9808574, Japan

[3] Tohoku Univ, Inst Dev Aging & Canc, Dept Pediat Oncol, Sendai, Miyagi 9808574, Japan

来源：

PEDIATRICS INTERNATIONAL | 2004年 / 46卷 / 05期

关键词：

22q11.2 deletion syndrome; autoimmune hemolytic anemia; DiGeorge syndrome; rituximab;

D O I：

10.1111/j.1442-200x.2004.01940.x

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

[No abstract available]

引用

页码：612 / 614

页数：3

共 50 条

[31] Otorhinologic Disorders in 22q11.2 Deletion Syndrome [J].

Lu, Nathan ;

Kacin, Alexa J. J. ;

Shaffer, Amber D. D. ;

Stapleton, Amanda L. L. .

OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2023, 169 (04) :1012-1019

[32] The Genetics and Epigenetics of 22q11.2 Deletion Syndrome [J].

Du, Qiumei ;

de la Morena, M. Teresa ;

van Oers, Nicolai S. C. .

FRONTIERS IN GENETICS, 2020, 10

[33] Chromatin Modifications in 22q11.2 Deletion Syndrome [J].

Zhe Zhang ;

LiHua Shi ;

Li Song ;

Kelly Maurer ;

Xue Zhao ;

Elaine H. Zackai ;

Daniel E. McGinn ;

T. Blaine Crowley ;

Donna M. McDonald McGinn ;

Kathleen E. Sullivan .

Journal of Clinical Immunology, 2021, 41 :1853-1864

[34] Clinical Manifestations of 22q11.2 Deletion Syndrome [J].

Cirillo, Annapaola ;

Lioncino, Michele ;

Maratea, Annachiara ;

Passariello, Annalisa ;

Fusco, Adelaide ;

Fratta, Fiorella ;

Monda, Emanuele ;

Caiazza, Martina ;

Signore, Giovanni ;

Esposito, Augusto ;

Baban, Anwar ;

Versacci, Paolo ;

Putotto, Carolina ;

Marino, Bruno ;

Pignata, Claudio ;

Cirillo, Emilia ;

Giardino, Giuliana ;

Sarubbi, Berardo ;

Limongelli, Giuseppe ;

Russo, Maria Giovanna .

HEART FAILURE CLINICS, 2022, 18 (01) :155-164

[35] Deletion Syndrome 22q11.2: A Systematic Review [J].

Cortes-Martin, Jonathan ;

Lopez Penuela, Nuria ;

Carlos Sanchez-Garcia, Juan ;

Montiel-Troya, Maria ;

Diaz-Rodriguez, Lourdes ;

Rodriguez-Blanque, Raquel .

CHILDREN-BASEL, 2022, 9 (08)

[36] Chromatin Modifications in 22q11.2 Deletion Syndrome [J].

Zhang, Zhe ;

Shi, LiHua ;

Song, Li ;

Maurer, Kelly ;

Zhao, Xue ;

Zackai, Elaine H. ;

McGinn, Daniel E. ;

Crowley, T. Blaine ;

McGinn, Donna M. McDonald ;

Sullivan, Kathleen E. .

JOURNAL OF CLINICAL IMMUNOLOGY, 2021, 41 (08) :1853-1864

[37] Endocrine aspects of the 22q11.2 deletion syndrome [J].

Weinzimer, SA .

GENETICS IN MEDICINE, 2001, 3 (01) :19-22

[38] Complement Activation in 22q11.2 Deletion Syndrome [J].

Grinde, Dina ;

Overland, Torstein ;

Lima, Kari ;

Schjalm, Camilla ;

Mollnes, Tom Eirik ;

Abrahamsen, Tore G. .

JOURNAL OF CLINICAL IMMUNOLOGY, 2020, 40 (03) :515-523

[39] Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome [J].

Montin, Davide ;

Marolda, Agostina ;

Licciardi, Francesco ;

Robasto, Francesca ;

Di Cesare, Silvia ;

Ricotti, Emanuela ;

Ferro, Francesca ;

Scaioli, Giacomo ;

Giancotta, Carmela ;

Amodio, Donato ;

Conti, Francesca ;

Giardino, Giuliana ;

Leonardi, Lucia ;

Ricci, Silvia ;

Volpi, Stefano ;

Baselli, Lucia Augusta ;

Azzari, Chiara ;

Bossi, Grazia ;

Consolini, Rita ;

Dellepiane, Rosa Maria ;

Duse, Marzia ;

Gattorno, Marco ;

Martire, Baldassarre ;

Putti, Maria Caterina ;

Soresina, Annarosa ;

Plebani, Alessandro ;

Ramenghi, Ugo ;

Martino, Silvana ;

Pignata, Claudio ;

Cancrini, Caterina .

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2019, 7 (07) :2369-2376

[40] Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome [J].

Colarusso, Gloria ;

Gambineri, Eleonora ;

Lapi, Elisabetta ;

Casini, Tommaso ;

Tucci, Fabio ;

Lippi, Francesca ;

Azzari, Chiara .

PEDIATRIC REPORTS, 2010, 2 (02) :42-43

← 1 2 3 4 5 →