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

Long term clinical follow up of four patients with Wolfram syndrome and urodynamic abnormalities.

Journal of pediatric endocrinology & metabolism : JPEM - 27 May 2024

Dange Nimisha S, Shah Nikhil, Oza Chirantap, Sharma Jyoti, Singhal Jyoti, Yewale Sushil, Mondkar Shruti, Ambike Shriniwas, Khadilkar Vaman, Khadilkar Anuradha V

Abstract excerpt

OBJECTIVES: Wolfram syndrome is characterised by insulin-dependent diabetes (IDDM), diabetes insipidus (DI), optic atrophy, sensorineural deafness and neurocognitive disorders. The DIDMOAD acronym has been recently modified to DIDMOAUD suggesting the rising awareness of the prevalence of urinary tract dysfunction (UD). End stage renal disease is the commonest cause of mortality in Wolfram syndrome. We present a...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diabetes Mellitus, Type 1

Share to Follow-Up Studies

Share to Membrane Proteins

Share to Mutation

Share to Prognosis

Share to Wolfram Syndrome

Source

Identifiers

PMID: 38465704
DOI: 10.1515/jpem-2023-0531

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Long term clinical follow up of four patients with Wolfram syndrome and urodynamic abnormalities.PMID 38465704Read ↗

Bladder dysfunction in Wolfram syndrome is highly prevalent and progresses to megacystis.Semantic proximity Read ↗

Wolfram Syndrome 1: A Pediatrician's and Pediatric Endocrinologist's Perspective.Semantic proximity Read ↗

Current developments in Wolfram syndrome.Semantic proximity Read ↗

Presentation and clinical course of Wolfram (DIDMOAD) syndrome from North India.Semantic proximity Read ↗

Severe Lower Urinary Tract Dysfunction in Otherwise Healthy Children: A Three-Case Series and Narrative ReviewSemantic proximity Read ↗

Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment?Semantic proximity Read ↗

Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus.Semantic proximity Read ↗

A new structural rearrangement associated to Wolfram syndrome in a child with a partial phenotype.Semantic proximity Read ↗

Clinical management and obstetric outcome in WFS1 Wolfram syndrome spectrum disorder: A case report and literature review.Semantic proximity Read ↗

Severe Lower Urinary Tract Dysfunction in Otherwise Healthy Children: Report of Three Cases and Review of the LiteratureSemantic proximity Read ↗

Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapy.Semantic proximity Read ↗

Long-term follow-up of a child with Wolcott-Rallison syndrome.Semantic proximity Read ↗

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