Pulmonary hypertension in a child with juvenile-type autosomal recessive polycystic kidney disease.

An 11 year-old girl, whose condition was diagnosed as juvenile-type autosomal recessive polycystic kidney disease (ARPKD) at five years of age, presented with chest pain and dyspnea that had developed suddenly two months previously. Two-dimensional echocardiography, Doppler study and cardiac cathete...

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Detalles Bibliográficos
Autores principales: Huh, J., Noh, C. I., Choi, J. Y., Yun, Y. S., Choi, Y., Seo, J. K.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1999
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054411/
https://www.ncbi.nlm.nih.gov/pubmed/10485628

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