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...
| Main Authors: | , , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Korean Academy of Medical Sciences
1999
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054411/ |