Mégarbané A, Souraty N, Theophile D, Vekemans M, Samaras L, Ghorayeb Z
Unité de Génétique Médicale, Faculté de Médecine, Université Saint-Joseph, Paris, France.
Ann Genet. 1997;40(1):55-9.
The authors describe a boy with a triangular face, wide forehead, telecanthus, large ears, prominent root of the nose, long and bulging philtrum, thin upper lip, everted lower lip, high arched palate, micrognathism, pointed chin, overriding toes, joint laxity, and mild mental retardation. Cytogenetic investigation disclosed the presence of an added chromosome, a very small acrocentric, consisting in the presence of the last band of the short arm of chromosome 17. This anomaly results from a 3:1 mal segregation of a balanced (13q17p) reciprocal maternal translocation leading to a trisomy 17pter. This is a previously undescribed chromosome anomaly.
作者描述了一名男孩,其面部呈三角形,额头宽阔,内眦间距增宽,耳朵大,鼻梁根部突出,人中长且隆起,上唇薄,下唇外翻,腭弓高,小颌畸形,下巴尖,脚趾重叠,关节松弛,且有轻度智力障碍。细胞遗传学检查发现存在一条额外的染色体,是一条非常小的近端着丝粒染色体,由17号染色体短臂的最后一条带组成。这种异常是由于平衡的(13q17p)母源相互易位发生3:1的减数分裂不分离,导致17号染色体短臂末端三体。这是一种此前未被描述过的染色体异常。