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

Cardiac arrhythmia in individuals with steroid sulfatase deficiency (X-linked ichthyosis): candidate anatomical and biochemical pathways

4 Apr 2024

Abstract excerpt

Circulating steroids, including sex hormones, can affect cardiac development and function. In mammals, steroid sulfatase (STS) is the enzyme solely responsible for cleaving sulfate groups from various steroid molecules, thereby altering their activity and water solubility. Recent studies have indicated that Xp22.31 genetic deletions encompassing STS (associated with the rare dermatological condition X-linked...

Read the complete abstract on PubMed

Topics

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

Share to Congenital heart defects research
Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypothalamic control of reproductive hormones

Source

Identifiers

PMID: 38571328
DOI: 10.1042/ebc20230098

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cardiac arrhythmia in individuals with steroid sulfatase deficiency (X-linked ichthyosis): candidate anatomical and biochemical pathwaysPMID 38571328Read ↗

Cardiac phenotype in children with X-linked ichthyosis (STS- sEDD): findings from a prospective cohortSemantic proximity Read ↗

X-Linked Ichthyosis: New Insights Into a Multi-System DisorderSemantic proximity Read ↗

Steroid sulfatase deficiency increases the frequency and persistence of ventricular arrhythmias in miceSemantic proximity Read ↗

Characterising heart rhythm abnormalities associated with Xp22.31 deletionSemantic proximity Read ↗

Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank.Semantic proximity Read ↗

Physiological and behavioural characterisation of a novel steroid sulfatase-deficient mouseSemantic proximity Read ↗

Revisiting X-linked congenital ichthyosis.Semantic proximity Read ↗

Sex-linked genetic mechanisms and atrial fibrillation risk.Semantic proximity Read ↗

Gender-specific genetic and epigenetic signatures in cardiovascular diseaseSemantic proximity Read ↗

Cardiovascular Phenotype in Turner Syndrome—Integrating Cardiology, Genetics, and EndocrinologySemantic proximity Read ↗

Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosisSemantic proximity Read ↗

Male sex hormone and reduced plakoglobin jointly impair atrial conduction and cardiac sodium currentsSemantic proximity Read ↗

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