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Genetic evaluation and management of fetal chylothorax: review and insights from a case of Noonan syndrome.
Chen, C H; Chen, T H; Kuo, S J; Chen, C P; Lee, D J; Ke, Y Y; Yeh, K T; Ma, G C; Liu, C S; Shih, J C; Chen, M.
Afiliação
  • Chen CH; Department of Obstetrics and Gynecology, Changhua Christian Hospital, Changhua, Taiwan.
Lymphology ; 42(3): 134-8, 2009 Sep.
Article em En | MEDLINE | ID: mdl-19927903
Fetal chylothorax is one of a very few syndromes that can be treated in utero with thoracoamniotic shunting or pleurodesis by OK-432 as two major therapeutic modalities. We report on a fetus with Noonan syndrome and a missense mutation c.182A > C (p.Asp61Ala) of PTPN11 who responded poorly to antenatal pleurodesis by OK-432. Based on our previous publication and this case study, we propose that fetal chylothorax of a distinct genetic origin may respond poorly to OK-432 pleurodesis.
Assuntos
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Base de dados: MEDLINE Assunto principal: Quilotórax / Síndrome de Noonan Idioma: En Ano de publicação: 2009 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Quilotórax / Síndrome de Noonan Idioma: En Ano de publicação: 2009 Tipo de documento: Article