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J Craniomaxillofac Surg ; 42(5): e91-6, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23953647

RESUMO

BACKGROUND: Features of Goldenhar syndrome include several craniofacial anomalies of structures derived from the first and second pharyngeal arches, as well as vertebral, cardiac and renal systems abnormalities. In addition, Goldenhar patients were reported to manifest a variety of central nervous system anomalies and several types of neoplasias. CASE HISTORY AND DISCUSSION: The first case of medulloblastoma in a patient with Goldenhar syndrome is presented here. There is no clear association between these two pathologies. We speculate that aberrant events during the migration of neural crest cells in early stages of development could be the basis of an association between medulloblastoma and Goldenhar syndrome. The case history suggests other possible etiological contributing factors to the development of medulloblastoma, such as patient's history of trauma and/or early childhood exposure to ionizing radiation.


Assuntos
Neoplasias Cerebelares/diagnóstico , Síndrome de Goldenhar/diagnóstico , Meduloblastoma/diagnóstico , Neoplasias Cerebelares/genética , Cromossomos Humanos Par 17/genética , Feminino , Seguimentos , Quarto Ventrículo/patologia , Síndrome de Goldenhar/genética , Humanos , Hidrocefalia/etiologia , Recém-Nascido , Isocromossomos/genética , Perda de Heterozigosidade/genética , Meduloblastoma/genética
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