polycystic liver disease造句

• Mutations of this gene have been linked with autosomal dominant polycystic liver disease.
• It is also associated with polycystic liver disease.
• Also, any mutation in this gene causes autosomal dominant polycystic liver disease . [ 7]
• When lymphangiomatosis occurs in the liver and / or spleen it may be confused with polycystic liver disease.
• Polycystic Liver Disease comes in two forms as ADPKD ( with kidney cysts ) and ADPLD ( liver cysts only ).
• They are classically associated with polycystic liver disease, as may be seen in the context of polycystic kidney disease, and represent a malformation of the liver plate.
• Currently recognized ciliopathies include Joubert syndrome, primary ciliary dyskinesia ( also known as Kartagener Syndrome ), Bardet-Biedl syndrome, polycystic kidney disease and polycystic liver disease, nephronophthisis, Alstrom syndrome, Meckel-Gruber syndrome and some forms of retinal degeneration.
• In an analysis of 20 patients from 9 unrelated families develop polycystic kidney disease with heterozygous mutations in the GANAB gene . 5 of the mutations from the GANAB gene were predicted to result in a short protein ( frameshift, nonsense, or splicing ), and 3 missense mutations . 7 of the families had a diagnosis of PKD, while the other 2 families had a diagnosis of polycystic liver disease ( PCLD ).