Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly

Autor(es)

Pereira Bertolacini, Claudia Danielli ^{[1, 2]} ; Richieri-Costa, Antonio ^[2] ; Ribeiro-Bicudo, Lucilene Arilho ^[2]

Afiliação do(s) autor(es)

^[1] Univ Estadual Paulista, Dept Genet, Botucatu, SP - Brazil

^[2] USP Bauru, Dept Genet, Hosp Reabilitacao Anomalias Craniofaciais, Bauru, SP - Brazil

• Tipo de documento: Artigo Científico
• Fonte: BRAIN & DEVELOPMENT; v. 32, n. 3, p. 217-222, MAR 2010.
• Citações Web of Science: 6

Resumo

Holoprosencephaly (HPE) is a malformation sequence where the cerebral hemispheres fail to separate into distinct left and right halves. It can be associated with midline structural anomalies of the central nervous system and/or face. SHH is the major gene implicated in HPE and it plays a critical role in early forebrain and central nervous system development. SHH is expressed in the human embryo in the notochord, the floorplate of the neural tube, and the posterior limb buds. In the present Study we performed mutational analysis of the entire coding region of the SHH gene in 37 Unrelated individuals with the HPE spectrum. Three different variants were found throughout the extent of the gene. No genotype-phenotype correlation is evident based oil the type or position of the mutations. This study confirms the great genetic heterogeneity of the disease and the difficulty to establish genotype-phenotype correlations. (C) 2009 Elsevier B.V. All rights reserved. (AU)

• Processo FAPESP: 03/00165-8 - Investigacao da interacao do gene msx1 nas formas nao-sindromicas das fissuras de labio e/ou palato.
• Beneficiário: Lucilene Arilho Ribeiro Bicudo
• Modalidade de apoio: Auxílio à Pesquisa - Regular
• Processo FAPESP: 06/60973-9 - Analise mutacional dos genes shh, tgif, six3, zic2, ptch e gli2 nas anomalias craniofaciais e alteracoes do desenvolvimento do sistema nervoso central.
• Beneficiário: Lucilene Arilho Ribeiro Bicudo
• Modalidade de apoio: Auxílio à Pesquisa - Regular