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卡波西肉瘤、口腔畸形、二尖瓣发育异常和脊柱侧弯与7q34-q36.3杂合性末端缺失相关。

Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated with 7q34-q36.3 heterozygous terminal deletion.

作者信息

Jackson Carolyn C, Lefèvre-Utile Alain, Guimier Anne, Malan Valérie, Bruneau Julie, Gessain Antoine, Cassar Olivier, Amiel Jeanne, Cobat Aurélie, Rattina Vimel, Abel Laurent, Casanova Jean-Laurent, Blanche Stéphane

机构信息

St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, New York.

Department of Pediatrics, The Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

Am J Med Genet A. 2017 Jul;173(7):1858-1865. doi: 10.1002/ajmg.a.38275. Epub 2017 May 9.

DOI:10.1002/ajmg.a.38275
PMID:28488400
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5680148/
Abstract

Chromosome 7 germline macrodeletions have been implicated in human congenital malformations and developmental delays. We herein report a novel heterozygous macrodeletion of 7q34-q36.3 in a 16-year-old girl originally from West Indies. Similar to previously reported cases of germline chromosome 7q terminal deletions, our patient has dental malposition, and developmental (growth and intellectual) delay. Novel phenotypic features include endemic Kaposi sarcoma (KS), furrowed tongue, thoracolumbar scoliosis, and mild mitral valve dysplasia. The occurrence of human herpes virus 8-driven KS, in a child otherwise normally resistant to other infectious agents and without any other tumoral lesion, points to a very selective immunodeficiency. While defects in organogenesis have been described with such macrodeletions, this is the first report of immunodeficiency and cancer predisposition.

摘要

7号染色体生殖系大片段缺失与人类先天性畸形和发育迟缓有关。我们在此报告一名来自西印度群岛的16岁女孩,其7号染色体q34-q36.3区域存在一种新的杂合性大片段缺失。与先前报道的生殖系7号染色体q末端缺失病例相似,我们的患者存在牙齿错位和发育(生长和智力)迟缓。新的表型特征包括地方性卡波西肉瘤(KS)、舌沟、胸腰椎脊柱侧凸和轻度二尖瓣发育异常。在一名对其他感染因子通常具有抵抗力且无任何其他肿瘤病变的儿童中发生人疱疹病毒8驱动的KS,提示存在非常选择性的免疫缺陷。虽然已有报道此类大片段缺失会导致器官发生缺陷,但这是首次报道免疫缺陷和癌症易感性。

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本文引用的文献

1
Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations.3例7号染色体长臂末端缺失的新病例及相关基因型和表型表现的文献综述
Am J Med Genet A. 2016 Apr;170A(4):896-907. doi: 10.1002/ajmg.a.37428. Epub 2016 Jan 29.
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Severe infectious diseases of childhood as monogenic inborn errors of immunity.儿童严重感染性疾病作为单基因遗传性免疫缺陷病
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Human genetic basis of interindividual variability in the course of infection.感染过程中个体间差异的人类遗传基础。
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Kaposi Sarcoma of Childhood: Inborn or Acquired Immunodeficiency to Oncogenic HHV-8.儿童卡波西肉瘤:对致癌性人疱疹病毒8型的先天性或获得性免疫缺陷。
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Viral profiling identifies multiple subtypes of Kaposi's sarcoma.病毒分析可识别卡波西肉瘤的多种亚型。
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The prevalence of chromosomal deletions relating to developmental delay and/or intellectual disability in human euploid blastocysts.人类整倍体囊胚中与发育迟缓及/或智力残疾相关的染色体缺失的发生率。
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