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

A Case of McLeod's Syndrome Presenting with Severe Decompensated Heart Failure.

Methodist DeBakey cardiovascular journal - 1 Jan 2023

Boppana Hemanth K, Thakkar Samarthkumar, Patel Harsh P, Bou Chaaya Rody G, Feitell Scott

Abstract excerpt

McLeod's syndrome (MLS) is an X-linked disorder caused by mutations in the XK gene with neurological manifestations as well as cardiomyopathy. This is a case of acute exacerbation of heart failure in a 44-year-old White male with a confirmed diagnosis of MLS, which was managed with guideline-directed medical therapy and placement of an implantable cardioverter defibrillator with recovery in ejection fraction.

Read the complete abstract on PubMed

Topics

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

Share to Defibrillators, Implantable
Share to Heart Failure

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 37720304
DOI: 10.14797/mdcvj.1164
PMCID: PMC10503528

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

A Case of McLeod's Syndrome Presenting with Severe Decompensated Heart Failure.PMID 37720304Read ↗

Dilative cardiomyopathy displaying double trouble etiology: Myocarditis and Mcleod syndrome?Semantic proximity Read ↗

Molecular Basis and Clinical Overview of McLeod Syndrome Compared With Other Neuroacanthocytosis SyndromesSemantic proximity Read ↗

McLeod syndrome with a novel XK frameshift mutation: A case report.Semantic proximity Read ↗

Novel XK mutation in a McLeod patient diagnosed after heart transplant.Semantic proximity Read ↗

McLeod syndrome: life-long neuropsychiatric disorder due to a novel mutation of the XK gene.Semantic proximity Read ↗

Cardiac Emerinopathy: A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction.Semantic proximity Read ↗

McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings.Semantic proximity Read ↗

Two McLeod patients with novel mutations in XK.Semantic proximity Read ↗

A novel c.82insC (p.Tyr28Leufs85X) mutation in the XK gene associated with the McLeod phenotype.Semantic proximity Read ↗

Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome.Semantic proximity Read ↗

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