Literature DB >> 23928108

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

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.
© 2013 Elsevier B.V. All rights reserved.

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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


  2 in total

1.  Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome.

Authors:  Gregorio Serra; Clara Giambrone; Vincenzo Antona; Francesca Cardella; Maurizio Carta; Marcello Cimador; Giovanni Corsello; Mario Giuffrè; Vincenzo Insinga; Maria Cristina Maggio; Marco Pensabene; Ingrid Anne Mandy Schierz; Ettore Piro
Journal:  Ital J Pediatr       Date:  2022-09-08       Impact factor: 3.288

2.  Optic nerve coloboma as extension of the phenotype of 22q11.23 duplication syndrome: a case report.

Authors:  Claudia Valencia-Peña; Paula Jiménez-Sanchez; Wilmar Saldarriaga; César Payán-Gómez
Journal:  BMC Ophthalmol       Date:  2020-08-17       Impact factor: 2.209

  2 in total

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