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猫眼综合征并垂体异常致生长激素缺乏症:病例报告及文献复习。

Cat eye syndrome and growth hormone deficiency with pituitary anomalies: a case report and review of the literature.

机构信息

Department of Paediatrics, Centro Hospitalar do Médio Ave, Portugal.

出版信息

Gene. 2013 Oct 15;529(1):186-9. doi: 10.1016/j.gene.2013.07.031. Epub 2013 Aug 6.

DOI:10.1016/j.gene.2013.07.031
PMID:23928108
Abstract

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.

摘要

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。

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Cat eye syndrome and growth hormone deficiency with pituitary anomalies: a case report and review of the literature.猫眼综合征并垂体异常致生长激素缺乏症:病例报告及文献复习。
Gene. 2013 Oct 15;529(1):186-9. doi: 10.1016/j.gene.2013.07.031. Epub 2013 Aug 6.
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引用本文的文献

1
Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome.新生儿患非家族性猫眼综合征,表现为先天性垂体功能减退和中线多处缺陷。
Ital J Pediatr. 2022 Sep 8;48(1):170. doi: 10.1186/s13052-022-01365-9.
2
Optic nerve coloboma as extension of the phenotype of 22q11.23 duplication syndrome: a case report.视神经缺损作为22q11.23重复综合征表型的扩展:一例报告
BMC Ophthalmol. 2020 Aug 17;20(1):333. doi: 10.1186/s12886-020-01603-w.