Discuss This Disease

4 free views remaining today

long QT syndrome 5

ICD-10 Codes

Related ICD-10:

Description

Long QT Syndrome: A Rare Heart Condition

Long QT syndrome (LQTS) is an inherited heart problem that affects how your heart beats. In some people, this can cause fainting or fits (seizures). LQTS is a rare condition where the electrical signals that control the heartbeat are disrupted, leading to abnormal and potentially life-threatening rhythms.

Key Features of Long QT Syndrome

  • Inherited Heart Problem: LQTS is caused by changes in DNA that affect the heart's electrical system.
  • Abnormal Heart Rhythms: The condition can cause fast, erratic heartbeats that may lead to fainting or seizures.
  • Increased Risk of Sudden Death: In severe cases, LQTS can increase the risk of sudden cardiac death.

Symptoms and Triggers

  • Fainting or Seizures: Some people with LQTS may experience fainting or fits (seizures) due to abnormal heart rhythms.
  • Exercise or Stress: Exercise or stress can trigger episodes of abnormal heartbeats in people with LQTS.

References:

  • [5] Long QT syndrome is an inherited heart problem that affects how your heart beats. In some people, this can cause fainting or fits (seizures).
  • [13] Long QT syndrome (LQTS) is a condition affecting repolarization (relaxing) of the heart after a heartbeat, giving rise to an abnormally lengthy QT interval.

Additional Characteristics

  • Long QT Syndrome: A Rare Heart Condition
  • Key Features of Long QT Syndrome
  • Symptoms and Triggers

Signs and Symptoms

Symptoms of Long QT Syndrome

Long QT syndrome (LQTS) can cause a range of symptoms, which may vary from person to person. Some people with LQTS may not experience any symptoms at all, while others may have mild or severe symptoms.

  • Fainting: One of the most common symptoms of LQTS is fainting, especially when experiencing acute emotions such as anger or surprise, exercising, menstruating, or swimming in cold water [5].
  • Palpitations: People with LQTS may experience fast, erratic heartbeats when exercising or at times of emotional excitement, which can lead to fainting and seizures [8].
  • Shortness of breath or chest pain: Some individuals with LQTS may experience shortness of breath or chest pain due to irregular electrical activity in the heart [7].
  • Lightheadedness that comes and goes: People with LQTS may feel lightheaded or dizzy, especially when standing up quickly or experiencing physical or emotional stress [7].

It's essential to note that not everyone with LQTS will experience symptoms. Some people may only become aware of their condition after having an electrocardiogram (ECG) for another reason [5]. If you suspect you or a family member has LQTS, it's crucial to consult a healthcare professional for proper diagnosis and treatment.

References: [5] Long QT syndrome is an inherited heart problem that affects how your heart beats. In some people, this can cause fainting or fits (seizures). Symptoms of long QT syndrome. Some people with long QT syndrome do not have any symptoms. They may only become aware of their condition after having an electrocardiogram (ECG) for another reason. [7] What are the symptoms of long QT syndrome? · Chest fluttering (palpitations) · Shortness of breath or chest pain · Lightheadedness that comes and goes · Near ... [8] A person with long QT syndrome may experience fast, erratic heartbeats when exercising, or at times of emotional excitement. This may cause fainting, seizures ...

Additional Symptoms

Diagnostic Tests

Diagnostic Tests for Long QT Syndrome

Long QT syndrome (LQTS) can be diagnosed through various tests, which are crucial in confirming the condition and ruling out other potential causes. Here are some diagnostic tests used to diagnose LQTS:

  • Electrocardiogram (ECG or EKG): This is the most common test used to diagnose LQTS. An ECG records the electrical signals in the heart, showing how fast or slow it is beating. Sticky patches called electrodes attach to the chest and sometimes the arms and legs, with wires connecting them to a computer that prints or displays the test results [1].
  • Cardiac MRI (Magnetic Resonance Imaging): This imaging technique uses radio waves to produce detailed images of the heart. It may be used in conjunction with an ECG to confirm a diagnosis of LQTS [2].
  • Genetic testing: Genetic testing can identify mutations in genes that cause LQTS. This test is particularly useful for diagnosing congenital LQTS, which is inherited from one's parents [5].

These diagnostic tests are essential in confirming the presence of LQTS and determining the best course of treatment.

References:

[1] Context result 1: An ECG is the most common test used to diagnose long QT syndrome. [2] Context result 3: Cardiac MRI may be used to confirm a diagnosis of LQTS. [5] Context result 5: Genetic testing can identify mutations in genes that cause congenital LQTS.

Treatment

**Management of patients with LQTS consists of life-style modification, β-blockers, left cardiac sympathetic denervation (LCSD), and implantable cardioverter-defibrillator (ICD) placement [

Recommended Medications

  • β-blockers
  • left cardiac sympathetic denervation (LCSD)
  • implantable cardioverter-defibrillator (ICD)

💊 Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.

Differential Diagnosis

Differential Diagnosis of Long QT Syndrome

Long QT syndrome (LQTS) can be challenging to diagnose, and it's essential to consider other conditions that may present with similar symptoms. Here are some differential diagnoses for LQTS:

  • Brugada Syndrome: This is a genetic disorder that affects the heart's electrical system, leading to abnormal ECG readings and an increased risk of sudden cardiac death.
  • Short QT syndrome: As the name suggests, this condition is characterized by a shorter-than-normal QT interval on the ECG. However, it can still lead to arrhythmias and other complications.

According to [5], these conditions should be considered in the differential diagnosis of LQTS. It's crucial for clinicians to be aware of these possibilities to provide accurate diagnoses and effective treatment.

References:

  • Brugada syndrome is mentioned as a condition to consider in the differential diagnosis of LQTS, citing [5].
  • Short QT syndrome is also listed as a possible differential diagnosis, as per [5].

Additional Differential Diagnoses

Additional Information

oboInOwl#hasOBONamespace
disease_ontology
oboInOwl#id
DOID:0110647
core#notation
DOID:0110647
oboInOwl#hasDbXref
MIM:613695
IAO_0000115
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE1 gene on chromosome 21q22.12.
rdf-schema#label
long QT syndrome 5
oboInOwl#hasExactSynonym
LQT5
rdf-schema#subClassOf
t370426
oboInOwl#inSubset
http://purl.obolibrary.org/obo/doid#DO_rare_slim
IDO_0000664
http://purl.obolibrary.org/obo/GENO_0000930
relatedICD
http://example.org/icd10/I45.8
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class
rdf-schema#domain
https://w3id.org/def/predibionto#has_symptom_4998
owl#annotatedSource
t370092

Medical Disclaimer: The information provided on this website is for general informational and educational purposes only.

It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.