Hervé B, Roume J, Cognard S, Fauvert D, Molina-Gomes D, Vialard F
Service de Cytogénétique, Centre Hospitalier Intercommunal de Poissy Saint-Germain-en-Laye, 10 rue du Champ Gaillard, F-78303 Poissy, France; UPCG, UFR des Sciences de la Santé Simone Veil, 2 avenue de la source de la Bièvre, F-78180 Montigny le Bretonneux, France.
Service de Cytogénétique, Centre Hospitalier Intercommunal de Poissy Saint-Germain-en-Laye, 10 rue du Champ Gaillard, F-78303 Poissy, France.
Eur J Med Genet. 2015 Jun-Jul;58(6-7):346-50. doi: 10.1016/j.ejmg.2015.04.005. Epub 2015 May 8.
Microdeletion and microduplication syndromes are well-known causes of developmental delay and/or malformations of differing severity. Although homogeneous abnormalities can now be detected relatively easily using microarray technologies, they are more difficult to detect and interpret in cases of mosaicism. Here, we report on a male infant with a mosaic de novo derivative chromosome 9, featuring a 10.2 Mb 5q35 duplication (including the NSD1 gene) and a 687 kb 9q34 deletion (including EHMT1). The infant presented developmental delay, short stature, brachy/plagiocephaly and hyperactivity. The proportion of abnormal cells was 50% in saliva (in a microarray analysis) and 25% in lymphocytes (in a FISH analysis). Despite the low-level mosaicism in lymphocytes, this imbalance appears to be responsible for a distinctive phenotype (suggesting the presence of variable clinical expression and/or major somatic mosaicism).
微缺失和微重复综合征是发育迟缓及不同严重程度畸形的常见病因。尽管现在使用微阵列技术相对容易检测到同源异常,但在嵌合体病例中更难检测和解释。在此,我们报告一例患有嵌合型新生衍生9号染色体的男婴,其特征为5q35区域有10.2 Mb的重复(包括NSD1基因)以及9q34区域有687 kb的缺失(包括EHMT1)。该婴儿表现出发育迟缓、身材矮小、短头/斜头畸形和多动。唾液中的异常细胞比例在微阵列分析中为50%,淋巴细胞中的异常细胞比例在荧光原位杂交分析中为25%。尽管淋巴细胞中的嵌合比例较低,但这种失衡似乎导致了一种独特的表型(提示存在可变的临床表型和/或主要的体细胞嵌合现象)。