Chopra Charu, Baretto Richard, Duddridge Michael, Browning Michael J
Department of Immunology, Leicester Royal Infirmary, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK.
Acta Paediatr. 2009 Feb;98(2):408-10. doi: 10.1111/j.1651-2227.2008.01077.x. Epub 2008 Oct 13.
CHARGE syndrome comprises coloboma of the eye, heart defects, choanal atresia, growth and developmental retardation, genitourinary anomalies and ear and hearing defects. The association between CHARGE syndrome and T-cell immunodeficiency is recognized, but has not been reported widely in the literature. We report four patients meeting the diagnostic criteria for CHARGE syndrome, who had moderate or severe T-cell lymphopenia complicated by infections. The patients presented in Leicester, UK, between 2000 and 2007. All patients were negative for 22q11.2 deletions by FISH analysis, but mutations in the CHD7 gene were identified in three patients in whom the analysis was performed. Our cases indicate that patients with CHARGE syndrome may have a spectrum of T-cell immune deficiency, and that this association may be more common than has previously been appreciated. We recommend that all patients diagnosed with CHARGE syndrome should have lymphocyte subsets evaluated as part of their initial investigation.
Thymic hypoplasia should be included in the clinical features associated with CHARGE syndrome. All patients with CHARGE syndrome should have lymphocyte subset analysis performed, to exclude T-cell immunodeficiency.
CHARGE综合征包括眼部缺损、心脏缺陷、后鼻孔闭锁、生长发育迟缓、泌尿生殖系统异常以及耳部和听力缺陷。CHARGE综合征与T细胞免疫缺陷之间的关联已得到认可,但在文献中尚未广泛报道。我们报告了4例符合CHARGE综合征诊断标准的患者,他们患有中度或重度T细胞淋巴细胞减少症并伴有感染。这些患者于2000年至2007年期间在英国莱斯特就诊。通过荧光原位杂交(FISH)分析,所有患者的22q11.2缺失均为阴性,但在进行分析的3例患者中发现了CHD7基因突变。我们的病例表明,CHARGE综合征患者可能存在一系列T细胞免疫缺陷,并且这种关联可能比之前认为的更为常见。我们建议,所有被诊断为CHARGE综合征的患者在初始检查时均应评估淋巴细胞亚群。
胸腺发育不全应纳入与CHARGE综合征相关的临床特征中。所有CHARGE综合征患者均应进行淋巴细胞亚群分析,以排除T细胞免疫缺陷。