Department of Paediatrics, Centro Hospitalar do Médio Ave, Portugal.
Gene. 2013 Oct 15;529(1):186-9. doi: 10.1016/j.gene.2013.07.031. Epub 2013 Aug 6.
Cat eye syndrome is a rare congenital disease characterized by the existence of a supernumerary chromosome derived from chromosome 22, with a variable phenotype comprising anal atresia, coloboma of the iris and preauricular tags or pits. We report a girl with cat eye syndrome, presenting short stature, with growth hormone deficiency due to posterior pituitary ectopia. Short stature is a common feature of this syndrome, and the association with a structural pituitary anomaly has been described, however growth hormone deficiency and the underlying mechanisms are rarely reported. A review on short stature and growth hormone deficiency in cat eye syndrome is conducted.
猫眼综合征是一种罕见的先天性疾病,其特征是存在一条源自 22 号染色体的额外染色体,其可变表型包括肛门闭锁、虹膜和前耳赘生物或窝。我们报告了一例患有猫眼综合征的女孩,身材矮小,因垂体后叶异位导致生长激素缺乏。身材矮小是该综合征的常见特征,并且已经描述了与结构性垂体异常的关联,但是生长激素缺乏及其潜在机制很少被报道。对猫眼综合征中身材矮小和生长激素缺乏进行了综述。