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 follow-up of a child with Wolcott-Rallison syndrome.

BMJ case reports - 13 May 2021

Shah Nikhil, Karguppikar Madhura Bharat, Khadilkar Vaman, Khadilkar Anuradha

Abstract excerpt

Wolcott-Rallison syndrome (WRS), the most common cause of permanent neonatal diabetes mellitus (DM) in consanguineous families, has a poor prognosis, with a mean survival of 5.8 years. Majority of children with WRS succumb to the disease in the first decade of life. We present the long-term follow-up of an 8-year-2-month-old girl with genetically proven WRS who was born to a non-consanguineous parentage. She is...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Diabetes Mellitus, Type 1
Share to eIF-2 Kinase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Follow-Up Studies

Share to Infant

Share to Infant, Newborn

Share to Osteochondrodysplasias

Source

Open in PubMed Open full text

Identifiers

PMID: 33986015
DOI: 10.1136/bcr-2021-242376
PMCID: PMC8126271

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Long-term follow-up of a child with Wolcott-Rallison syndrome.PMID 33986015Read ↗

Wolcott-Rallison syndrome: a case series of three patients.Semantic proximity Read ↗

Wolcott-Rallison syndrome.Semantic proximity Read ↗

Frequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review.Semantic proximity Read ↗

Natural history of Wolcott-Rallison syndrome: A systematic review and follow-up study.Semantic proximity Read ↗

Infantile-onset diabetes mellitus: a 1-year follow-up study.Semantic proximity Read ↗

Early-onset diabetes mellitus and neurodevelopmental retardation: the first Greek case of Wolcott-Rallison syndrome.Semantic proximity Read ↗

Lissencephaly-pachygyria spectrum in a North Indian boy with Wolcott-Rallison syndrome due to homozygous deletion of exon 1 in the EIF2AK3 gene.Semantic proximity Read ↗

EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndrome.Semantic proximity Read ↗

Variable phenotype in five patients with Wolcott-Rallison syndrome due to the same EIF2AK3 (c.1259delA) mutation.Semantic proximity Read ↗

Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families.Semantic proximity Read ↗

Liver disease and other comorbidities in Wolcott-Rallison syndrome: different phenotype and variable associations in a large cohort.Semantic proximity Read ↗

Os odontoideum in wolcott-rallison syndrome: a case series of 4 patients.Semantic proximity Read ↗

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