Literature DB >> 20371595

RAS-MAPK pathway disorders: important causes of congenital heart disease, feeding difficulties, developmental delay and short stature.

Emma M M Burkitt Wright1, Bronwyn Kerr.   

Abstract

The disorders described as the neuro-cardio-facio-cutaneous conditions (NCFCs) may all present with symptoms that are common in paediatric practice. They result from germline mutations in genes encoding kinases and other proteins interacting in the RAS-MAPK pathway. This review summarises these disorders, discussing their presenting features and clinical course, identifying overarching similarities and, conversely, features that can help to discriminate one condition from another. The genetic basis and importance of precise clinical diagnosis and molecular diagnostic confirmation when possible is discussed, given each condition's different prognosis, and the need to remain vigilant for specific complications.

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Year:  2010        PMID: 20371595     DOI: 10.1136/adc.2009.160069

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  9 in total

1.  Familial multiple lipomatosis with clear autosomal dominant inheritance and onset in early adolescence.

Authors:  Cheng-Hiang Lee; Roy A J Spence; Meena Upadhyaya; Patrick J Morrison
Journal:  BMJ Case Rep       Date:  2011-02-17

2.  LEOPARD Syndrome: Clinical Features and Gene Mutations.

Authors:  E Martínez-Quintana; F Rodríguez-González
Journal:  Mol Syndromol       Date:  2012-08-29

3.  Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations.

Authors:  Sarah Vergult; Ellen Van Binsbergen; Tom Sante; Silke Nowak; Olivier Vanakker; Kathleen Claes; Bruce Poppe; Nathalie Van der Aa; Markus J van Roosmalen; Karen Duran; Masoumeh Tavakoli-Yaraki; Marielle Swinkels; Marie-José van den Boogaard; Mieke van Haelst; Filip Roelens; Frank Speleman; Edwin Cuppen; Geert Mortier; Wigard P Kloosterman; Björn Menten
Journal:  Eur J Hum Genet       Date:  2013-10-09       Impact factor: 4.246

4.  Cutaneous features in 17q21.31 deletion syndrome: a differential diagnosis for cardio-facio-cutaneous syndrome.

Authors:  Emma Burkitt Wright; Dian Donnai; Diana Johnson; Jill Clayton-Smith
Journal:  Clin Dysmorphol       Date:  2011-01       Impact factor: 0.884

5.  Pierpont syndrome: a collaborative study.

Authors:  Emma M M Burkitt Wright; Mohnish Suri; Susan M White; Nicole de Leeuw; Anneke T Vulto-van Silfhout; Fiona Stewart; Shane McKee; Sahar Mansour; Fiona C Connell; Maya Chopra; Edwin P Kirk; Koen Devriendt; Willie Reardon; Han Brunner; Dian Donnai
Journal:  Am J Med Genet A       Date:  2011-08-10       Impact factor: 2.802

6.  Next Generation Sequencing Approach in a Prenatal Case of Cardio-Facio-Cutaneus Syndrome.

Authors:  Mafalda Mucciolo; Claudio Dello Russo; Laura D'Emidio; Alvaro Mesoraca; Claudio Giorlandino
Journal:  Int J Mol Sci       Date:  2016-06-16       Impact factor: 5.923

7.  Case report: Identification and clinical phenotypic analysis of novel mutation of the PPP1CB gene in NSLH2 syndrome.

Authors:  Xuemei He; Xiuli Ma; Jing Wang; Zhuo Zou; Haoyu Huang; Jian Ren; Chunming Liu; Nan Zheng; Jing Ma; Yun Liu
Journal:  Front Behav Neurosci       Date:  2022-09-08       Impact factor: 3.617

8.  Case report: Phenotype expansion and analysis of TRIO and CNKSR2 variations.

Authors:  Yuefang Liu; Zhe Liang; Weili Cai; Qixiang Shao; Qiong Pan
Journal:  Front Neurol       Date:  2022-08-29       Impact factor: 4.086

9.  Diagnostically relevant facial gestalt information from ordinary photos.

Authors:  Quentin Ferry; Julia Steinberg; Caleb Webber; David R FitzPatrick; Chris P Ponting; Andrew Zisserman; Christoffer Nellåker
Journal:  Elife       Date:  2014-06-24       Impact factor: 8.140

  9 in total

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