Skip to search formSkip to main contentSkip to account menu

Renal cysts and diabetes syndrome

Known as: Glomerulocystic kidney, familial hypoplastic, MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 5, CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT WITH DIABETES 
A condition associated with mutation(s) in the HNF1B gene or TCF2, characterized by renal cysts and early onset non-insulin dependent diabetes.(NICHD… 
National Institutes of Health

Related topics

Related topics

28 relations
Abnormal renal morphologyAsthenozoospermiaAutosomal dominant inheritanceBicornuate uterus

Broader (4)

CNS disorderCystic Kidney DiseasesDental EnamelDiabetes Mellitus, Non-Insulin-Dependent

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Hypertension as Determinant of Hyperuricemia: A Case Control Study from the Sub-Himalayan Region in North India.
Background Association between hyperuricemia and hypertension has been recognized for many years. Whether hyperuricemia is the… 
2013
2013
A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability
MODY5, renal cysts, and diabetes syndrome are autosomal dominant entities caused by mutation in the HNF1B gene. Here we report… 
Review
2007
Review
2007
Mechanism of injury in uromodulin-associated kidney disease.
Nephronophthisis (NPHP), medullary cystic kidney disease (MCKD), and familial juvenile hyperuricemic nephropathy (FJHN) are three… 
2006
2006
Renal hypoplasia and dysplasia: starting to put the puzzle together.
The human metanephros is the direct precursor of the mature kidney: It begins to form in the fifth gestational week, when… 
Review
2002
Review
2002
Recent insights into kidney diseases associated with glomerular cysts
Glomerular cysts can exist in the context of several different kidney diseases. Advances in the last few years have begun to… 
2002
2002
Severe hyperglycemia after renal transplantation in a pediatric patient with a mutation of the hepatocyte nuclear factor-1beta gene.
After renal transplantation for congenital cystic kidney disease of unknown origin, a 14-year-old boy, who was previously… 
2002
2002
Contributions to the MODY5 phenotype
We have previously presented a unique family of maturity-onset diabetes of the young, type 5 (MODY5) (McKusick 604284) who, in… 
2000
2000
New methodologies for interconnect reliability assessments of integrated circuits
The stringent performance and reliability demands that will accompany the development of next-generation circuits and new… 
1997
1997
Dietary alterations in plasma very low density lipoprotein levels modify renal excretion of urates in hyperuricemic-hypertriglyceridemic patients.
Hyperuricemic-hyperlipidemic patients exhibit decreased renal excretion of urates relative to purely hyperuricemic patients; also… 
Review
1996
Review
1996
Spectrum of glomerulocystic kidneys: a case report and review of the literature.
An 8-year-old boy developed end-stage renal disease 7 years after the in utero diagnosis of bilateral cystic kidneys. There was… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)