Literature DB >> 23613382

Expanding the phenotype of cardiovascular malformations in Adams-Oliver syndrome.

Claudia Algaze1, Edward D Esplin, Alexander Lowenthal, Louanne Hudgins, Theresa Ann Tacy, Elif Seda Selamet Tierney.   

Abstract

We describe a newborn with a phenotype consistent with Adams-Oliver syndrome and truncus arteriosus. Although cardiovascular malformations associated with this syndrome have been previously published in the literature, this is the first description of truncus arteriosus in a patient with Adams-Oliver syndrome. We review other reports of Adams-Oliver syndrome previously described with cardiovascular malformations, consider possible genetic and embryologic mechanisms, and emphasize the need for cardiology consultation when a diagnosis of Adams-Oliver syndrome is suspected in the differential diagnosis.
Copyright © 2013 Wiley Periodicals, Inc.

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Year:  2013        PMID: 23613382     DOI: 10.1002/ajmg.a.35864

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  8 in total

1.  Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome.

Authors:  Josephina A N Meester; Laura Southgate; Anna-Barbara Stittrich; Hanka Venselaar; Sander J A Beekmans; Nicolette den Hollander; Emilia K Bijlsma; Appolonia Helderman-van den Enden; Joke B G M Verheij; Gustavo Glusman; Jared C Roach; Anna Lehman; Millan S Patel; Bert B A de Vries; Claudia Ruivenkamp; Peter Itin; Katrina Prescott; Sheila Clarke; Richard Trembath; Martin Zenker; Maja Sukalo; Lut Van Laer; Bart Loeys; Wim Wuyts
Journal:  Am J Hum Genet       Date:  2015-08-20       Impact factor: 11.025

Review 2.  Extracellular O-linked β-N-acetylglucosamine: Its biology and relationship to human disease.

Authors:  Mitsutaka Ogawa; Koichi Furukawa; Tetsuya Okajima
Journal:  World J Biol Chem       Date:  2014-05-26

3.  Mutations in NOTCH1 cause Adams-Oliver syndrome.

Authors:  Anna-Barbara Stittrich; Anna Lehman; Dale L Bodian; Justin Ashworth; Zheyuan Zong; Hong Li; Patricia Lam; Alina Khromykh; Ramaswamy K Iyer; Joseph G Vockley; Rajiv Baveja; Ermelinda Santos Silva; Joanne Dixon; Eyby L Leon; Benjamin D Solomon; Gustavo Glusman; John E Niederhuber; Jared C Roach; Millan S Patel
Journal:  Am J Hum Genet       Date:  2014-08-14       Impact factor: 11.025

4.  Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants.

Authors:  Gavin Chapman; Julie L M Moreau; Eddie I P; Justin O Szot; Kavitha R Iyer; Hongjun Shi; Michelle X Yam; Victoria C O'Reilly; Annabelle Enriquez; Joelene A Greasby; Dimuthu Alankarage; Ella M M A Martin; Bernadette C Hanna; Matthew Edwards; Steven Monger; Gillian M Blue; David S Winlaw; Helen E Ritchie; Stuart M Grieve; Eleni Giannoulatou; Duncan B Sparrow; Sally L Dunwoodie
Journal:  Hum Mol Genet       Date:  2020-03-13       Impact factor: 6.150

5.  O-GlcNAc on NOTCH1 EGF repeats regulates ligand-induced Notch signaling and vascular development in mammals.

Authors:  Shogo Sawaguchi; Shweta Varshney; Mitsutaka Ogawa; Yuta Sakaidani; Hirokazu Yagi; Kyosuke Takeshita; Toyoaki Murohara; Koichi Kato; Subha Sundaram; Pamela Stanley; Tetsuya Okajima
Journal:  Elife       Date:  2017-04-11       Impact factor: 8.140

6.  Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies.

Authors:  Rajiv D Machado; Richard C Trembath; Laura Southgate; Maja Sukalo; Anastasios S V Karountzos; Edward J Taylor; Claire S Collinson; Deborah Ruddy; Katie M Snape; Bruno Dallapiccola; John L Tolmie; Shelagh Joss; Francesco Brancati; M Cristina Digilio; Luitgard M Graul-Neumann; Leonardo Salviati; Wiltrud Coerdt; Emmanuel Jacquemin; Wim Wuyts; Martin Zenker
Journal:  Circ Cardiovasc Genet       Date:  2015-05-11

Review 7.  Multifaceted regulation of Notch signaling by glycosylation.

Authors:  Ashutosh Pandey; Nima Niknejad; Hamed Jafar-Nejad
Journal:  Glycobiology       Date:  2021-01-09       Impact factor: 4.313

8.  Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry.

Authors:  Sarah Okashah; Dhanya Vasudeva; Aya El Jerbi; Houssein Khodjet-El-Khil; Mashael Al-Shafai; Najeeb Syed; Marios Kambouris; Sharda Udassi; Luis R Saraiva; Hesham Al-Saloos; Jai Udassi; Kholoud N Al-Shafai
Journal:  Genes (Basel)       Date:  2022-07-30       Impact factor: 4.141

  8 in total

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