17q12, uitgelegd voor kinderendeletion syndrome · static snapshot
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Gen + lichaamsdeel Nieren en diabetes 243 ondersteunende bronnen vertrouwen 97% nieuwheid 75%

Het gen HNF1B wordt in 135 verhalen genoemd samen met bloedsuikerproblemen (diabetes)

We lazen 135 verhalen die het over zowel het gen HNF1B als over bloedsuikerproblemen (diabetes) hebben. Dat betekent niet zeker dat het één het ander veroorzaakt, maar het komt wel vaak samen voor.

Hoe dit tot stand kwam

Dit gaat over wat er samen in de artikelen staat. Het is geen bewijs dat het ene het andere veroorzaakt.

Gegenereerd 2026-11-13, laatst gewijzigd vandaag. Dedup-sleutel assoc:HNF1B:diabetes_metabolic. De engine controleert dit inzicht bij elke analyse opnieuw; als meer bronnen het eens zijn, stijgen zijn onderbouwing en vertrouwen en verschijnt het opnieuw als “nieuw”.

Bewijs (6 citaten)

Corresponding author. Abstract Introduction Maturity-onset diabetes of the young (MODY) is a rare monogenic form of diabetes characterized by impaired insulin secretion and genetic and clinical heterogeneity. Accurate…
Corresponding author. Contributed equally. Abstract Background Beta-cell monogenic forms of diabetes have strong support for precision medicine. We systematically analyzed evidence for precision treatments for GCK-related hyperglycemia, HNF1A-, HNF4A…
Monogenic defects of beta cell function refer to a group of rare disorders that are characterized by early-onset diabetes mellitus due to a single gene mutation affecting insulin secretion. It accounts for up to 5% of all pediatric diabetes cases and includes transient o…
…xlx@zju.edu.cn (G.D.); chtang@zju.edu.cn (C.T.); Tel./Fax: +86-571-8706-1007 (C.T.) These authors contributed equally to this work. Abstract Neonatal Diabetes Mellitus (NDM) is a rare, heterogeneous monogenic disorder typically presenting within the first six months of life. Unlike type 1 or type 2 diabetes…
Academic Editor: Andrea Scaramuzza Objective Maturity-onset diabetes of the young (MODY) represents a genetically and clinically heterogeneous form of monogenic diabetes caused by defects in pancreatic β-cell function.…
…nding author. Abstract Context: Mutations in hepatocyte nuclear factor 1B ( HNF1B ) are rare but they are known to cause structural renal disease and diabetes mellitus. There is limited data on pediatric HNF1B disease. Objective: To analyze the clinical characteristics of HNF1B ‐related disease in a cohort…

Ondersteunende documenten (46)

VerhaalBronGepubliceerdGezienRelevantie
A Case of Amyotrophic Lateral Sclerosis With Coexisting Maturity-on... pubmed 2025-11-01 gisteren 1.00
17q12 Recurrent Deletion Syndrome in Childhood pmc 2025-01-01 gisteren 1.00
Atypical presentation of HNF1β gene mutation mimicking type 2 diabe... pmc 2025-01-01 gisteren 1.00
Precision treatment of beta-cell monogenic diabetes: a systematic review pmc 2024-01-01 gisteren 1.00
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and... pmc 2024-01-01 gisteren 1.00
A Korean Family Presenting with Renal Cysts and Maturity-Onset Diab... pmc 2024-01-01 gisteren 1.00
Monogenic Defects of Beta Cell Function: From Clinical Suspicion to... pmc 2024-01-01 gisteren 0.45
HNF1B Transcription Factor: Key Regulator in Renal Physiology and P... pmc 2024-01-01 gisteren 1.00
A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deleti... pmc 2024-01-01 gisteren 1.00
School level of children carrying a HNF1B variant or a deletion. pubmed 2020-01-01 gisteren 1.00
Maturity-onset diabetes of the young type 5, presenting as diabetic... pubmed 2022-05-01 gisteren 1.00
HNF1B-MODY Masquerading as Type 1 Diabetes: A Pitfall in the Etiolo... pubmed 2022-08-01 gisteren 1.00
The Clinical Characteristics and Gene Mutations of Maturity-Onset D... pubmed 2022-01-01 gisteren 1.00
Hepatocyte nuclear factor 1B deletion, but not intragenic mutation,... pubmed 2024-01-01 gisteren 1.00
Large Kidney Cysts in HNF1B Nephropathy Mimicking Autosomal Dominan... pubmed 2024-01-01 gisteren 1.00
Semaglutide as a potential therapeutic alternative for HNF1B-MODY: ... pubmed 2024-01-01 gisteren 1.00
HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic fea... pubmed 2026-01-01 gisteren 1.00
From Exome to Optical Mapping: Resolving a Complex 17q12 Rearrangem... pubmed 2026-10-09 gisteren 1.00
Type 1 Diabetes Polygenic Scores Improve Diagnostic Accuracy in Ped... pmc 2025-01-01 gisteren 1.00
A Case of Amyotrophic Lateral Sclerosis With Coexisting Maturity-on... pmc 2025-01-01 gisteren 1.00
MODY5 and 17q12 Microdeletion Syndrome: Phenotype Variability, Pren... pmc 2025-01-01 gisteren 1.00
HNF1β Gene Mutation Leading to a MODY5 With Renal Dysplasia: A Case Report pmc 2025-01-01 gisteren 1.00
Revealing Monogenic Diabetes: Clinical and Genetic Features of Pedi... pmc 2025-01-01 gisteren 1.00
From mutation to symptoms: a multi-center study on HNF1B -related n... pmc 2025-01-01 gisteren 1.00
HNF1B variant without hyperglycaemia as a cause of isolated profoun... pubmed 2023-02-09 gisteren 1.00
The Genetic Landscape and Precision Medicine in Neonatal Diabetes M... pmc 2026-01-01 gisteren 1.00
A complex microdeletion 17q12 phenotype in a patient with recurrent... pubmed 2012-05-14 gisteren 1.00
Identification of maturity-onset diabetes of the young through targ... pmc 2026-01-01 gisteren 1.00
Case Report: Nephrocalcinosis from pancreatic hypoplasia in HNF1B d... pmc 2026-01-01 gisteren 1.00
Pediatric Hepatocyte Nuclear Factor 1B ( HNF1B ) Disease: Diabetes ... pmc 2025-01-01 gisteren 1.00
A novel inversion at 17q12 disrupting HNF1B gene in a patient with ... pmc 2026-01-01 gisteren 1.00
Hepatic dysfunction, hyperuricemia, and multiple renal cysts in ado... pmc 2026-01-01 gisteren 1.00
Transient neonatal diabetes mellitus as an early diagnostic clue to... pmc 2026-01-01 gisteren 1.00
Functional validation of a non-canonical HNF1B splice-site variant in MODY5 pmc 2026-01-01 gisteren 1.00
17q12 deletion syndrome presenting with chronic pancreatitis: a case report pmc 2026-01-01 gisteren 1.00
Molecular impact of a novel HNF1B missense variant in childhood-ons... pmc 2026-01-01 gisteren 1.00
Type 1 Diabetes Polygenic Scores Improve Diagnostic Accuracy in Ped... pmc 2026-01-01 gisteren 1.00
HNF1B-MODY in the Norwegian MODY Registry and the Norwegian Childho... pmc 2026-01-01 gisteren 1.00
Insights from maturity-onset diabetes of the young into impaired in... pmc 2026-01-01 gisteren 1.00
HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic fea... pmc 2026-01-01 gisteren 1.00
HNF1B -related disease: developmental origins, molecular mechanisms... pmc 2026-01-01 gisteren 1.00
Treatment Options for Patients with Maturity-Onset Diabetes of the ... pmc 2026-01-01 gisteren 1.00
Clinical Spectrum and Early Renal Functional Variability in a Natio... pmc 2026-01-01 gisteren 1.00
Syndromic diabetes and hypergonadotropic hypogonadism in a boy with... pmc 2026-01-01 gisteren 1.00
Genetic Insights into Pediatric Polycystic Kidney Disease and Overl... pmc 2026-01-01 gisteren 1.00
PMC12903773 local_files - gisteren 1.00