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

Life-threatening cardiac arrhythmias in congenital central hypoventilation syndrome.

European journal of pediatrics - 1 May 2020

Laifman Eric, Keens Thomas G, Bar-Cohen Yaniv, Perez Iris A

Abstract excerpt

Congenital central hypoventilation syndrome (CCHS) patients are at risk for life-threatening cardiac arrhythmias, and presentation is dependent on their PHOX2B gene mutation. We describe the presentation of life-threatening arrhythmias in our cohort of CCHS patients. We reviewed the records of 72 CCHS patients seen at CHLA from 2004 to 2018. Data collected included demographics, PHOX2B genotype, ventilatory...

Read the complete abstract on PubMed

Topics

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

Share to Arrhythmias, Cardiac
Share to Child, Preschool
Share to Homeodomain Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypoventilation

Share to Risk Assessment

Share to Sleep Apnea, Central

Share to Transcription Factors

Share to Young Adult

Source

Identifiers

PMID: 31950261
DOI: 10.1007/s00431-019-03568-5

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

Life-threatening cardiac arrhythmias in congenital central hypoventilation syndrome.PMID 31950261Read ↗

Congenital central hypoventilation syndrome: diagnosis and management.Semantic proximity Read ↗

Guidelines for diagnosis and management of congenital central hypoventilation syndrome.Semantic proximity Read ↗

An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.Semantic proximity Read ↗

Transitional care and clinical management of adolescents, young adults, and suspected new adult patients with congenital central hypoventilation syndrome.Semantic proximity Read ↗

Central congenital hypoventilation syndrome: changing face of a less mysterious but more complex genetic disorder.Semantic proximity Read ↗

Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicine.Semantic proximity Read ↗

Later Onset Congenital Central Hypoventilation Syndrome.Semantic proximity Read ↗

Congenital central hypoventilation syndrome in korea: 20 years of clinical observation and evaluation of the ventilation strategy in a single center.Semantic proximity Read ↗

Anesthetic Considerations for Patients With Congenital Central Hypoventilation Syndrome: A Systematic Review of the Literature.Semantic proximity Read ↗

Extended clinical phenotype of late-onset congenital central hypoventilation syndrome in children with PHOX2B mutationsSemantic proximity Read ↗

The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype.Semantic proximity Read ↗

Congenital central hypoventilation syndrome: An overview of etiopathogenesis, associated pathologies, clinical presentation, and management.Semantic proximity Read ↗

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