Apert and Crouzon syndromes-Cognitive development, brain abnormalities, and molecular aspects

Author:

Fernandes Marilyse B. L.1,Maximino Luciana P.2,Perosa Gimol B.3,Abramides Dagma V. M.2,Passos-Bueno Maria Rita4,Yacubian-Fernandes Adriano23

Affiliation:

1. Hospital de Reabilitação de Anomalias Craniofaciais, USP; Bauru SP Brazil

2. Departamento de Fonoaudiologia; FOB-USP; Bauru SP Brazil

3. Departamento de Neurologia, Psicologia e Psiquiatria; UNESP; Botucatu SP Brazil

4. Instituto de Biociências, USP; São Paulo SP Brazil

Funder

São Paulo Research Foundation

Brazilian Federal Agency for the Support and Evaluation of Graduate Education

National Council for Scientific and Technological Development

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference48 articles.

1. Neuropsychological implications of Crouzon syndrome: A case report;Aguado;Rev Neurol,1999

2. Developmental aspects of oral language in craniosynostosis;Arduino-Meirelles;Pro Fono,2006

3. Health-related quality of life in children and adolescents with syndromic craniosynostosis;Bannink;J Plast Reconstr Aesthet Surg,2010

4. Crouzon's syndrome: Differential in vitro secretion of bFGF, TGFbeta I isoforms and extracellular matrix macromolecules in patients with FGFR2 gene mutation;Baroni;Cytokine,2002

5. Genes, cognition, and language: Some notes regarding velocardiofacial syndrome];Benítez;Neurologia,2009

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