An autosomal dominant pattern of transmission has been established for polycystic kidney disease. The degree of cystic involvement of other organs has been variable. The genetic pattern of transmission of polycystic liver disease independent of cystic kidney disease has never been established. We present a second family with polycystic liver disease without kidney disease. The lack of renal cysts is unlikely to be due to variable expressivity and penetrance of the gene for polycystic kidney disease. The liver cysts may be of late onset since none of the proband’s four children demonstrate cysts. Alternatively, none of these four individuals may have received the gene for polycystic liver disease from their affected mother. The family descri...
Autosomal dominant polycystic kidney disease is the most prevalent, potentially lethal, monogenic di...
Hitherto, mutations that lead to autosomal dominant adult-type polycystic kidney disease have been f...
Polycystic liver disease (PLD) is the result of embryonic ductal plate malformation of the intrahepa...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/65887/1/j.1399-0004.1982.tb01381.x.pd
Polycystic liver disease (PLD) is proven to occur either sporadically or in association with autosom...
Liver cysts are a commonly encountered phenomenon and may represent a broad cluster of disorders of ...
Polycystic liver disease (PLD) is characterized by the presence of multiple bile duct-derived epithe...
Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease. Congenital hepatic fibr...
Polycystic liver disease rarely occurs in isolation as part of autosomal dominant polycystic liver d...
BACKGROUND: Autosomal recessive polycystic kidney disease (ARPKD) shows a great phenotypic variabili...
Polycystic liver disease (PCLD, MIM 174050) is a dominantly inherited condition characterised by the...
The development of a polycystic liver is a characteristic of the monogenic disorders: autosomal domi...
Background. It is now well established that at least two genes are associated with autosomal dominan...
Autosomal recessive polycystic kidney disease (RPKD) (also called infantile polycystic kidney diseas...
: Autosomal dominant polycystic kidney disease (ADPKD) is the most common heritable multifocal cysti...
Autosomal dominant polycystic kidney disease is the most prevalent, potentially lethal, monogenic di...
Hitherto, mutations that lead to autosomal dominant adult-type polycystic kidney disease have been f...
Polycystic liver disease (PLD) is the result of embryonic ductal plate malformation of the intrahepa...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/65887/1/j.1399-0004.1982.tb01381.x.pd
Polycystic liver disease (PLD) is proven to occur either sporadically or in association with autosom...
Liver cysts are a commonly encountered phenomenon and may represent a broad cluster of disorders of ...
Polycystic liver disease (PLD) is characterized by the presence of multiple bile duct-derived epithe...
Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease. Congenital hepatic fibr...
Polycystic liver disease rarely occurs in isolation as part of autosomal dominant polycystic liver d...
BACKGROUND: Autosomal recessive polycystic kidney disease (ARPKD) shows a great phenotypic variabili...
Polycystic liver disease (PCLD, MIM 174050) is a dominantly inherited condition characterised by the...
The development of a polycystic liver is a characteristic of the monogenic disorders: autosomal domi...
Background. It is now well established that at least two genes are associated with autosomal dominan...
Autosomal recessive polycystic kidney disease (RPKD) (also called infantile polycystic kidney diseas...
: Autosomal dominant polycystic kidney disease (ADPKD) is the most common heritable multifocal cysti...
Autosomal dominant polycystic kidney disease is the most prevalent, potentially lethal, monogenic di...
Hitherto, mutations that lead to autosomal dominant adult-type polycystic kidney disease have been f...
Polycystic liver disease (PLD) is the result of embryonic ductal plate malformation of the intrahepa...