scholarly journals Angiotensinogen and Angiotensin II Type 1 Receptor Gene Polymorphism in Patients with Autosomal Dominant Polycystic Kidney Disease: Effect on Hypertension and ESRD

2003 ◽  
Vol 44 (4) ◽  
pp. 641 ◽  
Author(s):  
Kyu Beck Lee ◽  
Un Kyung Kim
Keyword(s):  
Angiotensin Ii ◽  
Kidney Disease ◽  
Gene Polymorphism ◽  
Autosomal Dominant ◽  
Receptor Gene ◽  
Polycystic Kidney ◽  
Receptor Gene Polymorphism ◽  
Autosomal Dominant Polycystic Kidney ◽  
Disease Effect

Angiotensin II Type 1 Receptor Gene Polymorphism in End-Stage Renal Disease

Nephron ◽  
2002 ◽  
Vol 92 (1) ◽  
pp. 51-55 ◽  
Author(s):  
Monika Buraczynska ◽  
Piotr Ksiazek ◽  
Wojciech Zaluska ◽  
Danuta Spasiewicz ◽  
Teresa Nowicka ◽  
...  
Keyword(s):  
Angiotensin Ii ◽  
Gene Polymorphism ◽  
Renal Disease ◽  
End Stage Renal Disease ◽  
Receptor Gene ◽  
Receptor Gene Polymorphism ◽  
Stage Renal Disease ◽  
End Stage

scholarly journals Genetic Mutations in Autosomal Dominant Polycystic Kidney Disease Type-1

2019 ◽  
Vol 04 (01) ◽  
Author(s):  
Chandra Sanwal ◽  
Karim Nooruddin ◽  
Chirag Patel ◽  
Tiannan Zhang ◽  
Anita Bhagavathula ◽  
...  
Keyword(s):  
Kidney Disease ◽  
Polycystic Kidney Disease ◽  
Autosomal Dominant ◽  
Disease Type ◽  
Genetic Mutations ◽  
Polycystic Kidney ◽  
Autosomal Dominant Polycystic Kidney

Rhombencephalosynapsis associated with autosomal dominant polycystic kidney disease Type 1

2008 ◽  
Vol 2 (6) ◽  
pp. 435-437 ◽  
Author(s):  
Robert Elliott ◽  
David H. Harter
Keyword(s):  
Kidney Disease ◽  
Polycystic Kidney Disease ◽  
Autosomal Dominant ◽  
Chromosomal Abnormalities ◽  
Disease Type ◽  
Clear Pattern ◽  
Polycystic Kidney ◽  
Cerebellar Peduncles ◽  
Autosomal Dominant Polycystic Kidney

Rhombencephalosynapsis (RES) is a rare congenital malformation of the cerebellum characterized by hypogenesis or agenesis of the vermis and fusion of the cerebellar hemispheres with or without fusion of the dentate nuclei and superior cerebellar peduncles. No genetic or chromosomal abnormalities have been identified for RES. Although the occurrence of RES is presumed to be sporadic, no clear pattern of inheritance has been identified. The authors report on a 17-year-old girl with autosomal dominant polycystic kidney disease Type 1 as well as RES.

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