| Literature DB >> 23928108 |
Cláudia Melo1, Susana Gama-de-Sousa, Filipa Almeida, Paula Rendeiro, Purificação Tavares, Helena Cardoso, Sónia Carvalho.
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.Entities:
Keywords: ACTH; CES; Cat eye syndrome; FISH; FT4; GH; Growth hormone deficiency; HESX homeobox 1; HESX1; IGF-1; IGF-BP3; LHX4; LIM homeobox 4; MLPA; MRI; Posterior pituitary ectopia; SD; Short stature; TSH; adrenocorticotropic hormone; cat eye syndrome; fluorescent in situ hybridization; free total thyroxine; growth hormone; insulin growth factor 1; insulin growth factor binding protein 3; inv dup(22)(q11); magnetic resonance imaging; multiplex ligation-dependent probe amplification; sample deviation; thyroid-stimulating hormone or thyrotropin
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Year: 2013 PMID: 23928108 DOI: 10.1016/j.gene.2013.07.031
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688