Dipartimento Materno Infantile, Università di Palermo, via Cardinale Rampolla 1, 90142, Palermo, Italy.
Eur J Pediatr. 2010 Jul;169(7):845-51. doi: 10.1007/s00431-009-1128-4. Epub 2010 Jan 21.
Interstitial deletions of the long arm of chromosome 14 are relatively rare. We report a 8.5-year-old girl with dysmorphic facial features and mental retardation associated with a de novo interstitial deletion of chromosome 14. The comparison between our patient and all published patients is reviewed. The genetic investigations have allowed us to define the critical chromosomal region and to start an accurate follow-up.
14 号染色体长臂的片段缺失较为罕见。我们报道了一例 8.5 岁的女孩,具有畸形的面部特征和智力障碍,与一条 14 号染色体的新生片段缺失有关。我们对该患者与所有已发表的患者进行了比较。遗传研究使我们能够确定关键的染色体区域,并开始进行准确的随访。