Garre's Osteomyelitis in a Patient With Chromosome 22q11.2 Syndrome: A Case Report

被引：5
|
作者：
Spinnato, Gaetano [1 ]
Agnihotri, Neil [1 ]
Ziccardi, Vincent B. [1 ]
机构：
[1] Univ Med & Dent New Jersey, New Jersey Dent Sch, Dept Oral & Maxillofacial Surg, Newark, NJ 07103 USA
来源：
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY | 2011年 / 69卷 / 06期
关键词：
DIGEORGE-SYNDROME; DELETION; DISEASE;
D O I：
10.1016/j.joms.2010.01.016
中图分类号：
R78 [口腔科学];
学科分类号：
1003 ;
摘要：
[No abstract available]
引用
收藏
页码：E75 / E77
页数：3
相关论文
共 50 条
  • [21] Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patients
    Repetto, G. M.
    Guzman, M. L.
    Puga, A.
    Calderon, J. F.
    Astete, C. P.
    Aracena, M.
    Arriaza, M.
    Aravena, T.
    Sanz, P.
    CLINICAL GENETICS, 2009, 76 (05) : 465 - 470
  • [22] Clinical and Immunological Defects and Outcomes in Patients with Chromosome 22q11.2 Deletion Syndrome
    Yu, Hsin-Hui
    Chien, Yin-Hsiu
    Lu, Meng-Yao
    Hu, Ya-Chiao
    Lee, Jyh-Hong
    Wang, Li-Chieh
    Lin, Yu-Tsan
    Yang, Yao-Hsu
    Chiang, Bor-Luen
    JOURNAL OF CLINICAL IMMUNOLOGY, 2022, 42 (08) : 1721 - 1729
  • [23] A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases
    Vaz, Sara O.
    Pires, Renato
    Pires, Luis M.
    Carreira, Isabel M.
    Anjos, Rui
    Maciel, Paula
    Mota-Vieira, Luisa
    BMC PEDIATRICS, 2015, 15
  • [24] Wilms Tumor in a Patient With 22q11.2 Microdeletion
    Finch, Paul T.
    Pivnick, Eniko K.
    Furman, Wayne
    Odom, Christine C.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (05) : 1162 - 1164
  • [25] Developmental trajectories in 22q11.2 deletion syndrome
    Swillen, Ann
    McDonald-McGinn, Donna
    AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2015, 169 (02) : 172 - 181
  • [26] Neurological manifestation of 22q11.2 deletion syndrome
    Bayat, Michael
    Bayat, Allan
    NEUROLOGICAL SCIENCES, 2022, 43 (03) : 1695 - 1700
  • [27] Immunological aspects of 22q11.2 deletion syndrome
    Gennery, A. R.
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2012, 69 (01) : 17 - 27
  • [28] Various Psychiatric Manifestation in DiGeorge Syndrome (22q11.2 Deletion Syndrome): A Case Report
    Kim, Giok
    Moon, Eunsoo
    Park, Je Min
    Lee, Byung Dae
    Lee, Young Min
    Jeong, Hee Jeong
    Kim, Soo Yeon
    Lee, Kangyoon
    Suh, Hwagyu
    CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE, 2020, 18 (03) : 458 - 462
  • [29] Endocrine aspects of the 22q11.2 deletion syndrome
    Weinzimer, SA
    GENETICS IN MEDICINE, 2001, 3 (01) : 19 - 22
  • [30] Complement Activation in 22q11.2 Deletion Syndrome
    Grinde, Dina
    Overland, Torstein
    Lima, Kari
    Schjalm, Camilla
    Mollnes, Tom Eirik
    Abrahamsen, Tore G.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2020, 40 (03) : 515 - 523
12345