» Articles » PMID: 20371595

RAS-MAPK Pathway Disorders: Important Causes of Congenital Heart Disease, Feeding Difficulties, Developmental Delay and Short Stature

Overview
Journal Arch Dis Child
Specialty Pediatrics
Date 2010 Apr 8
PMID 20371595
Citations 11
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

An Unexpected Finding of a PTPN11 Germline Mutation in a Patient With a Melanocytic Lesion With a Somatic MAP2K1 Mutation. Coincidence or Not?.

van der Woude S, Klein Wassink-Ruiter J, Kluiver J, de Jonge M, Diercks G J Cutan Pathol. 2024; 52(1):20-23.

PMID: 39392019 PMC: 11652124. DOI: 10.1111/cup.14730.


Identification of necroptosis-related diagnostic biomarkers in coronary heart disease.

You H, Han W Heliyon. 2024; 10(9):e30269.

PMID: 38726127 PMC: 11079106. DOI: 10.1016/j.heliyon.2024.e30269.


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

He X, Ma X, Wang J, Zou Z, Huang H, Ren J Front Behav Neurosci. 2022; 16:987259.

PMID: 36160684 PMC: 9492974. DOI: 10.3389/fnbeh.2022.987259.


Case report: Phenotype expansion and analysis of and variations.

Liu Y, Liang Z, Cai W, Shao Q, Pan Q Front Neurol. 2022; 13:948877.

PMID: 36105777 PMC: 9465251. DOI: 10.3389/fneur.2022.948877.


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

Mucciolo M, Dello Russo C, DEmidio L, Mesoraca A, Giorlandino C Int J Mol Sci. 2016; 17(6).

PMID: 27322245 PMC: 4926485. DOI: 10.3390/ijms17060952.