Literature DB >> 30024444

Cardiovascular disease in Noonan syndrome.

Mary Ella Pierpont1,2, Maria Cristina Digilio3.   

Abstract

PURPOSE OF REVIEW: To provide information on the scope of cardiac disease in Noonan syndrome. RECENT
FINDINGS: Noonan syndrome is a common autosomal dominant RASopathy disorder characterized by clinical findings of facial dysmorphism, congenital heart disease, and short stature. The degree of genetic heterogeneity has recently become evident in that Noonan syndrome is now known to be caused by mutations in a large variety of genes which produce dysregulation of the RAS-MAPK (mitogen-activated protein kinase) signaling pathway. The scope of cardiac disease in Noonan syndrome is quite variable depending on the gene mutation, with some mutations usually associated with a high incidence of congenital heart defects (PTPN11, KRAS, and others) while those with predominantly hypertrophic cardiomyopathy (HCM) have higher risk and morbidity profiles (RAF1, RIT1, and those associated with multiple lentigines).
SUMMARY: Cardiac disease in Noonan syndrome varies according to the type of gene mutation. The most common forms of cardiac disease include pulmonary stenosis, HCM, and atrial septal defect. HCM in general is associated with increased risk, mortality, and morbidity. New concepts for potential treatments are discussed.

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Year:  2018        PMID: 30024444     DOI: 10.1097/MOP.0000000000000669

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  9 in total

Review 1.  An Assessment of the Therapeutic Landscape for the Treatment of Heart Disease in the RASopathies.

Authors:  Jae-Sung Yi; Sravan Perla; Anton M Bennett
Journal:  Cardiovasc Drugs Ther       Date:  2022-02-14       Impact factor: 3.727

Review 2.  22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects.

Authors:  Carolina Putotto; Flaminia Pugnaloni; Marta Unolt; Stella Maiolo; Matteo Trezzi; Maria Cristina Digilio; Annapaola Cirillo; Giuseppe Limongelli; Bruno Marino; Giulio Calcagni; Paolo Versacci
Journal:  Children (Basel)       Date:  2022-05-25

3.  Generation of an induced pluripotent stem cell line (TRNDi003-A) from a Noonan syndrome with multiple lentigines (NSML) patient carrying a p.Q510P mutation in the PTPN11 gene.

Authors:  Rong Li; Amanda Baskfield; Yongshun Lin; Jeanette Beers; Jizhong Zou; Chengyu Liu; Fabrice Jaffré; Amy E Roberts; Elizabeth A Ottinger; Maria I Kontaridis; Wei Zheng
Journal:  Stem Cell Res       Date:  2018-12-26       Impact factor: 2.020

4.  Noonan syndrome patient-specific induced cardiomyocyte model carrying SOS1 gene variant c.1654A>G.

Authors:  Narasimman Gurusamy; Sheeja Rajasingh; Vinoth Sigamani; Reshma Rajasingh; Dona Greta Isai; Andras Czirok; Douglas Bittel; Johnson Rajasingh
Journal:  Exp Cell Res       Date:  2021-02-04       Impact factor: 3.905

5.  Application of CRISPR-Cas9 gene editing for congenital heart disease.

Authors:  Heeyoung Seok; Rui Deng; Douglas B Cowan; Da-Zhi Wang
Journal:  Clin Exp Pediatr       Date:  2021-03-02

6.  Double-chambered right ventricle complicated by hypertrophic obstructive cardiomyopathy diagnosed as Noonan syndrome.

Authors:  Masahiro Yamamoto; Seiji Takashio; Naoya Nakashima; Shinsuke Hanatani; Yuichiro Arima; Kenji Sakamoto; Eiichiro Yamamoto; Koichi Kaikita; Yoko Aoki; Kenichi Tsujita
Journal:  ESC Heart Fail       Date:  2020-02-20

7.  Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations.

Authors:  Jeevana Praharsha Athota; Meenakshi Bhat; Sheela Nampoothiri; Kalpana Gowrishankar; Sanjeeva Ghanti Narayanachar; Vinuth Puttamallesh; Mohammed Oomer Farooque; Swathi Shetty
Journal:  BMC Med Genet       Date:  2020-03-12       Impact factor: 2.103

8.  Differences in severity of cardiovascular anomalies in children with Noonan syndrome based on the causative gene.

Authors:  Nagham Shehade-Awwad; Yonatan Yeshayahu; Orit Pinhas-Hamiel; Uriel Katz
Journal:  Front Pediatr       Date:  2022-09-08       Impact factor: 3.569

9.  The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations.

Authors:  Geeske M van Woerden; Richelle Senden; Charlotte de Konink; Rossella A Trezza; Anwar Baban; Jennifer A Bassetti; Yolande van Bever; Lynne M Bird; Bregje W van Bon; Alice S Brooks; Qiaoning Guan; Eric W Klee; Carlo Marcelis; Joel M Rosado; Lisa A Schimmenti; Amy R Shikany; Paulien A Terhal; Kathryn Nicole Weaver; Marja W Wessels; Hester van Wieringen; Anna C Hurst; Catherine F Gooch; Katharina Steindl; Pascal Joset; Anita Rauch; Marco Tartaglia; Marcello Niceta; Ype Elgersma; Serwet Demirdas
Journal:  Hum Mutat       Date:  2022-07-29       Impact factor: 4.700

  9 in total

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