Literature DB >> 21536246

[Rasopathies: developmental disorders that predispose to cancer and skin manifestations].

A Hernández-Martín1, A Torrelo.   

Abstract

Proteins belonging to the RAS/mitogen activated protein kinase (MAPK) pathway play key roles in cell proliferation, differentiation, survival, and death. For more than 30 years now we have known that 30% of human cancers carry somatic mutations in genes encoding proteins from this pathway. Whereas somatic mutations have a high malignant potential, germline mutations are linked to developmental abnormalities that are often poorly clinically differentiated, although each is dependent upon the specific gene affected. Thus, all patients share varying degrees of mental retardation or learning difficulties, heart disease, facial dysmorphism, skin anomalies, and, in some cases, predisposition to cancer. These syndromes, known as rasopathies, include Noonan syndrome, Costello syndrome, neurofibromatosis-1, LEOPARD syndrome, cardiofaciocutaneous syndrome, and Legius syndrome. Recognizing the skin manifestations of rasopathies can facilitate diagnosis of these syndromes.
Copyright © 2011 Elsevier España, S.L. y AEDV. All rights reserved.

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Year:  2011        PMID: 21536246     DOI: 10.1016/j.ad.2011.02.010

Source DB:  PubMed          Journal:  Actas Dermosifiliogr        ISSN: 0001-7310


  6 in total

1.  Distinct Clinical and Pathological Features of Melorheostosis Associated With Somatic MAP2K1 Mutations.

Authors:  Smita Jha; Nadja Fratzl-Zelman; Paul Roschger; Georgios Z Papadakis; Edward W Cowen; Heeseog Kang; Tanya J Lehky; Katharine Alter; Zuoming Deng; Aleksandra Ivovic; Lauren Flynn; James C Reynolds; Abhijit Dasgupta; Markku Miettinen; Eileen Lange; James Katz; Klaus Klaushofer; Joan C Marini; Richard M Siegel; Timothy Bhattacharyya
Journal:  J Bone Miner Res       Date:  2018-09-14       Impact factor: 6.741

2.  RASopathies: Presentation at the Genome, Interactome, and Phenome Levels.

Authors:  Urska Pevec; Neva Rozman; Blaz Gorsek; Tanja Kunej
Journal:  Mol Syndromol       Date:  2016-04-21

3.  Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene.

Authors:  Francesca Mercadante; Ettore Piro; Martina Busè; Emanuela Salzano; Arturo Ferrara; Gregorio Serra; Cristina Passarello; Giovanni Corsello; Maria Piccione
Journal:  Ital J Pediatr       Date:  2022-08-19       Impact factor: 3.288

4.  Tegumentary manifestations of Noonan and Noonan-related syndromes.

Authors:  Caio Robledo D'Angioli Costa Quaio; Tatiana Ferreira de Almeida; Amanda Salem Brasil; Alexandre C Pereira; Alexander A L Jorge; Alexsandra C Malaquias; Chong Ae Kim; Débora Romeo Bertola
Journal:  Clinics (Sao Paulo)       Date:  2013       Impact factor: 2.365

5.  Craniomaxillofacial morphology alterations in children, adolescents and adults with neurofibromatosis 1: A cone beam computed tomography analysis of a Brazilian sample.

Authors:  E-B Luna; M-E-R Janini; F Lima; R-R-A Pontes; F-R Guedes; M Geller; L-E da Silva; A-T Motta; K-S Cunha
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2018-03-01

6.  miRNA Genetic Variants Alter Their Secondary Structure and Expression in Patients With RASopathies Syndromes.

Authors:  Joseane Biso de Carvalho; Guilherme Loss de Morais; Thays Cristine Dos Santos Vieira; Natana Chaves Rabelo; Juan Clinton Llerena; Sayonara Maria de Carvalho Gonzalez; Ana Tereza Ribeiro de Vasconcelos
Journal:  Front Genet       Date:  2019-11-13       Impact factor: 4.599

  6 in total

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