1.
Indian J Pathol Microbiol
;
1995 Oct; 38(4): 435-8
Artigo
em Inglês
| IMSEAR
| ID: sea-74600
RESUMO
Autosomal Recessive Polycystic Kidney (ARPKD) is a very rare entity (1 in 15,000 live births) and mostly not compatible with life. Early diagnosis and genetic councelling may help prevent such births. Two interested cases are presented.