Abstract
The disease presentation of autosomal recessive polycystic kidney disease (OMIM #263200, ARPKD) is highly variable and includes polycystic kidneys, pulmonary hypoplasia, and congenital hepatic fibrosis. The authors report an unusual case of ARPKD presenting with hepatosplenornegaly and cytopenia mimicking acute leukemia
Lingua originale | English |
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pagine (da-a) | 567-568 |
Numero di pagine | 2 |
Rivista | JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY |
Volume | 27 |
Stato di pubblicazione | Published - 2005 |
All Science Journal Classification (ASJC) codes
- ???subjectarea.asjc.2700.2735???
- ???subjectarea.asjc.2700.2720???
- ???subjectarea.asjc.2700.2730???