Kisho

Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy

intermediate DEND syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

intermediate DEND syndrome

MONDO:0020569

Also known as:developmental delay-epilepsy-neonatal diabetes syndrome, intermediate form

Overview

Intermediate DEND syndrome (iDEND) is a rare mild form of DEND syndrome, a neonatal diabetes mellitus, developmental delay and epilepsy condition. The intermediate form is characterized clinically by mild motor, speech or cognitive delay and an absence of epilepsy.

ResearchLimited published research (4 articles)

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for intermediate DEND syndrome.

4 publications have been identified in PubMed for intermediate DEND syndrome. Research spans Review / Meta-Analysis (50%), Case Report / Case Series (25%), and Basic Science / Preclinical (25%).

Recent Publications

Plengvidhya N (2026). [PMID: 41498801](https://pubmed.ncbi.nlm.nih.gov/41498801/). *Hum Genet*. [Basic Science / Preclinical]
Abreu GM (2025). [PMID: 41169283](https://pubmed.ncbi.nlm.nih.gov/41169283/). *Front Clin Diabetes Healthc*. [Case Report / Case Series]
Saadati S (2025). [PMID: 41376626](https://pubmed.ncbi.nlm.nih.gov/41376626/). *Front Immunol*. [Review / Meta-Analysis]
Gobble MRS (2025). [PMID: 40128490](https://pubmed.ncbi.nlm.nih.gov/40128490/). *Curr Diab Rep*. [Review / Meta-Analysis]

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 2:11 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:99989

GARD

Genetic and Rare Diseases Info Center

GARD:19724

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

← Back to All Diseases

intermediate DEND syndrome

Overview

Prognosis

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team