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Microcephaly, lissencephaly, Hirschsprung disease and tetralogy of Fallot: a new syndrome?
Tanteles, George A; Kurup, Beena; Rauch, Anita; Splitt, Miranda P.
Afiliação
  • Tanteles GA; Institute of Human Genetics, International Centre for Life, Newcastle upon Tyne, UK.
Clin Dysmorphol ; 15(2): 107-10, 2006 Apr.
Article em En | MEDLINE | ID: mdl-16531738
We report an 8-month-old girl with extreme microcephaly, lissencephaly, tetralogy of Fallot and Hirschsprung disease. She has a history of infantile spasms with developmental stagnation. Various diagnoses were considered but none seem to fit her clinical presentation. This combination of findings has not been described in the past and we suggest that this may be a previously undescribed neurodevelopmental syndrome resulting from a global failure of neuronal migration.
Assuntos
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Base de dados: MEDLINE Assunto principal: Tetralogia de Fallot / Lisencefalia / Doença de Hirschsprung / Microcefalia Limite: Adult / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2006 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Tetralogia de Fallot / Lisencefalia / Doença de Hirschsprung / Microcefalia Limite: Adult / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2006 Tipo de documento: Article