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Clin Genet ; 82(1): 71-6, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21651513

RESUMO

. The relationship of mutations in the patched gene PTCH and nevoid basal cell carcinoma (NBCC) or Gorlin syndrome is well established. Animal studies have implicated the hedgehog-patched signalling pathway in neurulation and neural tube defects (NTDs). Spina bifida occulta and bifid vertebrae are well recognized in NBCCS, but there appears to be only one report of open spina bifida. We report a father and two sons with a truncating PTCH mutation and the major features of NBCCS. One son had open thoracic spina bifida and the other had an occipital meningocoele. We believe this to be the first report of cranial NTD in NBCCS and suggest that consideration be given to including PTCH analysis in genetic association studies in NTDs as the hedgehog pathway is integral to normal human neurulation.


Assuntos
Síndrome do Nevo Basocelular/genética , Encefalocele/genética , Tubo Neural/metabolismo , Receptores de Superfície Celular/genética , Espinha Bífida Oculta/genética , Adulto , Síndrome do Nevo Basocelular/patologia , Códon sem Sentido , Análise Mutacional de DNA , Encefalocele/patologia , Éxons , Haploinsuficiência , Humanos , Masculino , Pessoa de Meia-Idade , Tubo Neural/patologia , Receptores Patched , Receptor Patched-1 , Espinha Bífida Oculta/patologia
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