Literature DB >> 31229977

BMPR1A mutation-positive juvenile polyposis syndrome and atrial septal defect: coincidence or association?

Rachel E Harris1, Richard K Russell1.   

Abstract

We describe the case of a 16-year-old male patient with BMPR1A mutation and incidentally detected atrial septal defect (ASD). This patient was diagnosed with BMPR1A mutation through genetic testing and was attending for routine surveillance endoscopy when ASD was incidentally diagnosed. He was referred to cardiology outpatient clinic with plans for elective ASD closure. Through this case report we aim to discuss the pathophysiology of juvenile polyposis syndrome (JPS), highlight what we believe to be a novel presentation of comorbid BMPR1A mutation and ASD and hypothesise that patients with BMPR1A mutation and JPS may be at risk of previously unrecognised cardiovascular complications analogous to the previous association of SMAD4 JPS and cardiac abnormalities. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  cardiovascular medicine; gastroenterology; genetics

Mesh:

Substances:

Year:  2019        PMID: 31229977      PMCID: PMC6605934          DOI: 10.1136/bcr-2019-229881

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  7 in total

1.  Hereditary hamartomatous polyposis syndromes: understanding the disease risks as children reach adulthood.

Authors:  Michael Manfredi
Journal:  Gastroenterol Hepatol (N Y)       Date:  2010-03

Review 2.  Juvenile polyposis syndrome.

Authors:  Lodewijk Aa Brosens; Danielle Langeveld; W Arnout van Hattem; Francis M Giardiello; G Johan A Offerhaus
Journal:  World J Gastroenterol       Date:  2011-11-28       Impact factor: 5.742

3.  Juvenile colonic polyposis associated with congenital heart disease.

Authors:  L Onaran; B Sahin; G Temucin; A Gököz
Journal:  Dis Colon Rectum       Date:  1978-10       Impact factor: 4.585

4.  Novel Association of Juvenile Polyposis Syndrome With Atrial Septal Aneurysm and Patent Foramen Ovale: A Case Report.

Authors:  Melanio Bruceta; Luisa De Souza; Zyad Carr; Anthony Bonavia; Kunal Karamchandani
Journal:  A A Pract       Date:  2018-06-15

5.  A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).

Authors:  Carol J Gallione; Gabriela M Repetto; Eric Legius; Anil K Rustgi; Susan L Schelley; Sabine Tejpar; Grant Mitchell; Eric Drouin; Cornelius J J Westermann; Douglas A Marchuk
Journal:  Lancet       Date:  2004-03-13       Impact factor: 79.321

6.  Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review.

Authors:  Karen E Wain; Marissa S Ellingson; Jamie McDonald; Amanda Gammon; Maegan Roberts; Pavel Pichurin; Ingrid Winship; Douglas L Riegert-Johnson; Jeffrey N Weitzel; Noralane M Lindor
Journal:  Genet Med       Date:  2014-02-13       Impact factor: 8.822

7.  Juvenile polyposis syndrome.

Authors:  Wojciech Cichy; Beata Klincewicz; Andrzej Plawski
Journal:  Arch Med Sci       Date:  2014-06-27       Impact factor: 3.318

  7 in total

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