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

Molecular Characterization and Management of Congenital Hyperinsulinism: A Tertiary Centre Experience.

Indian pediatrics - 15 Feb 2022

Sharma Rajni, Roy Kakali, Satapathy Amit Kumar, Kumar Anil, Nanda Pamali Mahasweta, Damle Nishikant, Houghton Jayne A L, Flanagan Sarah E, Radha Venkatesan, Mohan Viswanathan, Jain Vandana

Abstract excerpt

BACKGROUND: There is limited data from India regarding medical management of congenital hyperinsulinism (CHI). OBJECTIVE: To study the molecular diagnosis, medical management and outcomes of children with CHI. STUDY DESIGN: Ambispective. SETTING: PARTICIPANTS: Children with CHI admitted in from December, 2011 till March, 2020 at a tertiary care referral hospital. OUTCOMES: Clinical and genetic profile,...

Topics

Join the communities discussing this publication.

Child
Child, Preschool
Congenital Hyperinsulinism
Diazoxide
Infant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Infant, Newborn

Quality of Life

Sulfonylurea Receptors

Source

Open in PubMed Open full text

Identifiers

PMID: 34992182
PMCID: PMC8913199

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular Characterization and Management of Congenital Hyperinsulinism: A Tertiary Centre Experience.PMID 34992182Read ↗

Genetic and Clinical Characterisation of Congenital Hyperinsulinism: Identification of a Novel ABCC8 Variant.Semantic proximity Read ↗

Diagnosis and treatment of a newborn with congenital hyperinsulinemia:Case report and literature reviewSemantic proximity Read ↗

Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital HyperinsulinismSemantic proximity Read ↗

Characterization of Congenital Hyperinsulinism in Argentina: Clinical Features, Genetic Findings, and Treatment OutcomesSemantic proximity Read ↗

Congenital hyperinsulinism in Chinese patients: 5-yr treatment outcome of 95 clinical cases with genetic analysis of 55 cases.Semantic proximity Read ↗

Genetic characteristics and long-term follow-up of 11 patients with congenital hyperinsulinism followed in a single center.Semantic proximity Read ↗

Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations.Semantic proximity Read ↗

Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.Semantic proximity Read ↗

Congenital hyperinsulinism: current trends in diagnosis and therapySemantic proximity Read ↗

Congenital hyperinsulinism in infancy and childhood: challenges, unmet needs and the perspective of patients and familiesSemantic proximity Read ↗

Evaluation and management of neonatal onset hyperinsulinemic hypoglycemia: a single neonatal center experience.Semantic proximity Read ↗

Congenital hyperinsulinism: recent updates on molecular mechanisms, diagnosis and management.Semantic proximity Read ↗

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