Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A rare combination of MODY5 and duodenal atresia in a patient: a case report.

BMC medical genetics - 6 Feb 2020

Du Tao, Zeng Nan, Wen Xiaofang, Zhu Peizhuang, Li Wangen

Abstract excerpt

BACKGROUND: Maturity-onset diabetes of the young (MODY) is a genetically and clinically heterogeneous group of hereditary diabetes, generally caused by one abnormal gene. MODY5 is caused by mutations of the hepatocyte nuclear factor 1 homeobox β gene (HNF1β), always as a part of Chr17q12 deletion, whereas heterozygous mutation in B lymphocyte kinase (BLK) gene is responsible for MODY11. CASE PRESENTATION: We...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Diabetes Mellitus, Type 2
Share to Hepatocyte Nuclear Factor 1-beta
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Insulin

Share to Mutation

Share to Phenotype

Share to src-Family Kinases

Source

Open in PubMed Open full text

Identifiers

PMID: 32028929
DOI: 10.1186/s12881-020-0954-0
PMCID: PMC7006404

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A rare combination of MODY5 and duodenal atresia in a patient: a case report.PMID 32028929Read ↗

Maturity-onset diabetes of the young (MODY): an update.Semantic proximity Read ↗

Revealing Monogenic Diabetes: Clinical and Genetic Features of Pediatric MODY Cases in Türkiye: Single Center Experience.Semantic proximity Read ↗

Monogenic Defects of Beta Cell Function: From Clinical Suspicion to Genetic Diagnosis and Management of Rare Types of Diabetes.Semantic proximity Read ↗

HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic features-two case reports.Semantic proximity Read ↗

The Clinical Characteristics and Gene Mutations of Maturity-Onset Diabetes of the Young Type 5 in Sixty-One Patients.Semantic proximity Read ↗

Genetic Variants and Therapeutic Approaches in Maturity-Onset Diabetes of the Young: A Retrospective AnalysisSemantic proximity Read ↗

Genetics and Pathophysiology of Maturity-onset Diabetes of the Young (MODY): A Review of Current TrendsSemantic proximity Read ↗

Maturity onset diabetes of the young: identification and diagnosis.Semantic proximity Read ↗

Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future PerspectivesSemantic proximity Read ↗

Clinical and laboratory clues of maturity-onset diabetes of the young and determination of association with molecular diagnosis.Semantic proximity Read ↗

Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype RelationshipSemantic proximity Read ↗

MODY Only Monogenic? A Narrative Review of the Novel Rare and Low-Penetrant Variants.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.