Literature DB >> 14760276

IMAGe syndrome: a complex disorder affecting growth, adrenal and gonadal function, and skeletal development.

C C Pedreira1, R Savarirayan, Margaret R Zacharin.   

Abstract

IMAGe syndrome (intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities; MIM 300290) is a multisystem disorder with a broad phenotype, which, if unrecognized, may result in major and possibly life-threatening complications. Initial clinical features overlap with those of Russell-Silver syndrome (RSS) and isolated growth hormone (GH) deficiency, conditions from which it must be distinguished. We report an Australian male with adrenal hypoplasia congenita (AHC) in association with IMAGe syndrome. The patient had intrauterine growth restriction (IUGR) and dysmorphic features comprising small, low-set ears, micrognathia, bilateral cryptorchidism, micropenis, and skeletal abnormalities. Signs of adrenal insufficiency occurred at aged 4.6 years. Our patient differs from those previously described by the late onset of adrenal insufficiency and the presence of GH deficiency. IMAGe is a complex syndrome involving dysmorphic features; disorders of growth, gonadal, and adrenal function; and skeletal abnormalities.

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Year:  2004        PMID: 14760276     DOI: 10.1016/j.jpeds.2003.09.052

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  10 in total

1.  A case of a Korean newborn with IMAGe association presenting with hyperpigmented skin at birth.

Authors:  Jung Min Ko; Jung Hyun Lee; Gu-Hwan Kim; Ai-Rhan Kim; Han-Wook Yoo
Journal:  Eur J Pediatr       Date:  2006-11-22       Impact factor: 3.183

2.  Anesthetic and dental management of a child with IMAGe syndrome.

Authors:  Rochelle G Lindemeyer; Stephanie E Rashewsky; Phillip J Louie; Laura Schleelein
Journal:  Anesth Prog       Date:  2014

3.  Conditional mutagenesis of Gata6 in SF1-positive cells causes gonadal-like differentiation in the adrenal cortex of mice.

Authors:  Marjut Pihlajoki; Elisabeth Gretzinger; Rebecca Cochran; Antti Kyrönlahti; Anja Schrade; Theresa Hiller; Laura Sullivan; Michael Shoykhet; Erica L Schoeller; Michael D Brooks; Markku Heikinheimo; David B Wilson
Journal:  Endocrinology       Date:  2013-03-07       Impact factor: 4.736

4.  Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome.

Authors:  Valerie A Arboleda; Hane Lee; Rahul Parnaik; Alice Fleming; Abhik Banerjee; Bruno Ferraz-de-Souza; Emmanuèle C Délot; Imilce A Rodriguez-Fernandez; Debora Braslavsky; Ignacio Bergadá; Esteban C Dell'Angelica; Stanley F Nelson; Julian A Martinez-Agosto; John C Achermann; Eric Vilain
Journal:  Nat Genet       Date:  2012-05-27       Impact factor: 38.330

5.  Is Hyperpigmentation on the First Day of Life Always Associated with IMAGe Syndrome?

Authors:  Elif Özsu; Rahime Gül Yeşiltepe Mutlu; Olcay Işık; Filiz Mine Çizmecioğlu; Şükrü Hatun
Journal:  J Clin Res Pediatr Endocrinol       Date:  2014-12

Review 6.  Beckwith-Wiedemann and IMAGe syndromes: two very different diseases caused by mutations on the same gene.

Authors:  Donatella Milani; Lidia Pezzani; Silvia Tabano; Monica Miozzo
Journal:  Appl Clin Genet       Date:  2014-09-16

Review 7.  Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms.

Authors:  Megan Schmit; Anja-Katrin Bielinsky
Journal:  Int J Mol Sci       Date:  2021-01-18       Impact factor: 5.923

8.  Increased protein stability of CDKN1C causes a gain-of-function phenotype in patients with IMAGe syndrome.

Authors:  Naoki Hamajima; Yoshikazu Johmura; Satoshi Suzuki; Makoto Nakanishi; Shinji Saitoh
Journal:  PLoS One       Date:  2013-09-30       Impact factor: 3.240

9.  DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency.

Authors:  Clare V Logan; Jennie E Murray; David A Parry; Andrea Robertson; Roberto Bellelli; Žygimantė Tarnauskaitė; Rachel Challis; Louise Cleal; Valerie Borel; Adeline Fluteau; Javier Santoyo-Lopez; Tim Aitman; Inês Barroso; Donald Basel; Louise S Bicknell; Himanshu Goel; Hao Hu; Chad Huff; Michele Hutchison; Caroline Joyce; Rachel Knox; Amy E Lacroix; Sylvie Langlois; Shawn McCandless; Julie McCarrier; Kay A Metcalfe; Rose Morrissey; Nuala Murphy; Irène Netchine; Susan M O'Connell; Ann Haskins Olney; Nandina Paria; Jill A Rosenfeld; Mark Sherlock; Erin Syverson; Perrin C White; Carol Wise; Yao Yu; Margaret Zacharin; Indraneel Banerjee; Martin Reijns; Michael B Bober; Robert K Semple; Simon J Boulton; Jonathan J Rios; Andrew P Jackson
Journal:  Am J Hum Genet       Date:  2018-11-29       Impact factor: 11.025

Review 10.  The Genetic Backdrop of Hypogonadotropic Hypogonadism.

Authors:  Anna Szeliga; Michal Kunicki; Marzena Maciejewska-Jeske; Natalia Rzewuska; Anna Kostrzak; Blazej Meczekalski; Gregory Bala; Roman Smolarczyk; Eli Y Adashi
Journal:  Int J Mol Sci       Date:  2021-12-08       Impact factor: 5.923

  10 in total

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