Esophageal dysbiosis refers to an imbalance in the normal microbial community of the esophagus. Under healthy conditions, the esophageal mucosa hosts a diverse population of bacteria—predominantly Gram-positive species such as Streptococcus spp.—that help maintain barrier integrity and modulate local immune responses. When this balanced ecosystem is disrupted, overgrowth of pathobionts (often Gram-negative bacteria like Escherichia coli or Fusobacterium nucleatum) can occur, leading to inflammation, increased epithelial permeability, and symptom generation such as heartburn, chest pain, or dysphagia BioMed CentralBiocodex Microbiota Institute.

In patients with gastroesophageal reflux disease (GERD) or functional esophageal disorders, studies have shown a marked shift toward Gram-negative bacteria, which interact with toll-like receptors (TLRs) on esophageal epithelial cells to trigger cytokine release (e.g., IL-6), downregulate tight-junction proteins (e.g., claudin-1), and dilate intercellular spaces (DIS), thereby compromising the mucosal barrier BioMed Central. Chronic dysbiosis may also contribute to the progression of Barrett’s esophagus and esophageal adenocarcinoma by promoting pro-carcinogenic inflammation PMCcancerbiomed.org.

Esophageal dysbiosis refers to an imbalance in the communities of microorganisms—bacteria, fungi, and viruses—that normally live in the lining of the esophagus. In a healthy esophagus, these microbes exist in a balanced state, helping to protect the lining, aid digestion, and train the local immune system. When that balance is disrupted—so that some species grow too much while others diminish—this is called dysbiosis. Dysbiosis can impair the barrier function of the esophageal lining, allowing acid, enzymes, or pathogens to damage the tissue and trigger inflammation PMC.


Types of Esophageal Dysbiosis

Although research is ongoing, clinicians often recognize four broad patterns of esophageal microbial imbalance:

  1. Bacterial Overgrowth Dysbiosis
    Too many acid-tolerant bacteria (e.g., certain Proteobacteria) flourish, crowding out beneficial species.

  2. Fungal Dominance Dysbiosis
    An overabundance of yeasts (often Candida species) adheres to and invades the esophageal lining BioMed Central.

  3. Viral Dysbiosis
    Changes in resident viruses (the “virome”) alter interactions with both bacteria and the host immune system, potentially worsening inflammation.

  4. Mixed-Community Dysbiosis
    Simultaneous overgrowth of bacteria, fungi, or viruses creates a complex imbalance that’s harder to correct.

Each type may present subtly different symptoms and may respond best to tailored therapies—such as targeted probiotics for bacterial dysbiosis or antifungal treatments for fungal overgrowth MDPI.


Common Causes

Microbial imbalances in the esophagus can arise from many factors. Below are 20 well-documented contributors:

  1. Proton-Pump Inhibitor (PPI) Use
    Reduces stomach acid, enabling normally suppressed bacteria to overgrow.

  2. Broad-Spectrum Antibiotics
    Kill off beneficial microbes, allowing opportunistic species to dominate Cleveland Clinic.

  3. Frequent Acid Reflux (GERD)
    Acid injures the lining, making it easier for harmful microbes to adhere and flourish PMC.

  4. Diet High in Processed Sugars
    Feeds yeast like Candida, promoting fungal overgrowth.

  5. Alcohol Consumption
    Disrupts mucosal immunity and damages microbial balance.

  6. Smoking
    Alters local immunity and microbial composition.

  7. Immunosuppression
    From medications (e.g., steroids) or conditions (e.g., HIV), lowers defense against opportunistic microbes.

  8. Diabetes Mellitus
    High blood sugar can fuel microbial growth, especially yeasts.

  9. Obesity
    Linked to low-grade inflammation that perturbs the microbiome.

  10. Poor Oral Hygiene
    Oral pathogens can seed the esophagus when swallowed.

  11. Hiatal Hernia
    Promotes reflux and mucosal injury, creating a niche for dysbiosis.

  12. Scleroderma (Esophageal Involvement)
    Impaired motility leads to stasis and microbial overgrowth.

  13. Achalasia
    Ineffective esophageal clearance allows microbes to accumulate.

  14. Chemotherapy and Radiotherapy
    Damage mucosal barriers and alter microbial niches.

  15. Environmental Toxins
    Pollutants and food additives can disrupt microbial balance Cleveland Clinic.

  16. Chronic Psychological Stress
    Modulates gut–brain axis signals, affecting microbial communities.

  17. Dietary Imbalances (Low Fiber)
    Fiber helps maintain a healthy microbiome; low intake harms diversity.

  18. Helicobacter pylori Infection
    Alters gastric acidity and downstream microbial populations.

  19. Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)
    Cause mucosal injury that can foster dysbiosis.

  20. Genetic Factors
    Variants in immune genes (e.g., TLRs) can predispose individuals to dysbiosis.


Symptoms

Esophageal dysbiosis often contributes to—or mimics—the following symptoms:

  1. Difficulty Swallowing (Dysphagia)
    Feeling as if food sticks in the throat.

  2. Painful Swallowing (Odynophagia)
    Sharp pain when swallowing liquids or solids.

  3. Heartburn or Burning Sensation
    A burning feeling behind the breastbone.

  4. Chest Pain
    Not related to heart issues—often worse with swallowing.

  5. Regurgitation
    Sour or bitter fluid coming back up into the mouth.

  6. Nausea or Vomiting
    Feeling sick in the stomach or actual vomiting.

  7. Globussensation
    Feeling a lump or foreign object in the throat.

  8. Persistent Cough
    Chronic cough from irritation.

  9. Hoarseness
    Changes in your voice due to laryngeal irritation.

  10. Food Impaction
    Solid food getting lodged in the esophagus, sometimes requiring removal.

  11. Unexplained Weight Loss
    Avoidance of eating because of pain or discomfort.

  12. Bad Breath (Halitosis)
    Microbial breakdown of food in a slowed or stagnant esophagus.

  13. Throat Clearing
    Frequent need to clear mucus caused by irritation.

  14. Anemia
    Chronic bleeding from inflamed lining can lower red blood cells.

  15. Fatigue
    General tiredness from nutrient loss and chronic inflammation.

Many of these arise as dysbiosis disrupts acid clearance and triggers low-grade inflammation in the esophageal lining MDPIPMC.


Diagnostic Tests

To confirm esophageal dysbiosis and rule out other disorders, clinicians employ a combination of tests:

Physical Exam

  1. General Vital Signs
    To detect fever or anemia.

  2. Neck and Chest Palpation
    To assess lymphadenopathy or tenderness.

Manual (Functional) Tests

  1. High-Resolution Esophageal Manometry
    Measures muscle contractions to detect motility disorders (achalasia, scleroderma) that predispose to dysbiosis Wikipedia.

  2. 24-Hour pH Monitoring
    Quantifies acid exposure, correlating reflux with symptoms.

  3. Bravo™ Wireless pH Capsule
    Records esophageal pH over days without nasal catheter.

Laboratory & Pathological

  1. Esophageal Mucosal Biopsy Culture
    Grows bacteria/fungi from biopsy samples.

  2. Histology with Special Stains
    Identifies fungal hyphae (PAS stain) or eosinophils (H&E stain).

  3. 16S rRNA Gene Sequencing
    Profiles bacterial communities in biopsy or brushings.

  4. Polymerase Chain Reaction (PCR) Panels
    Detects specific pathogens (e.g., Candida, Herpesviridae).

  5. Complete Blood Count (CBC)
    Checks for anemia or elevated white cells.

  6. Serum Inflammatory Markers
    CRP and ESR to gauge systemic inflammation.

  7. Serum IgE Levels
    Elevated in allergic esophagitis (EoE) overlap.

Electrodiagnostic

  1. Impedance Monitoring
    Detects non-acid reflux and correlates with symptoms.

  2. Electrogastrography
    Rarely used, records esophageal myoelectric activity.

Imaging Tests

  1. Upper GI Endoscopy
    Direct visualization of mucosal inflammation, rings, furrows; allows biopsy Wikipedia.

  2. Barium Swallow (Esophagram)
    Shows strictures, rings (“feline esophagus”), or diverticula.

  3. Endoscopic Ultrasound (EUS)
    Assesses wall layers and submucosal involvement.

  4. CT Scan of Chest
    Detects wall thickening or complications (e.g., perforation).

  5. MRI of Mediastinum
    Occasionally used to evaluate masses or fibrosis.

  6. PET–CT Scan
    Rules out neoplastic causes of dysbiosis-like findings.


Non-Pharmacological Treatments

Below are twenty evidence-based therapies and lifestyle strategies that restore microbial balance, improve mucosal defense, and relieve symptoms. Each is described with its purpose and proposed mechanism.

  1. Probiotic Lozenges

    • Description: Slow-dissolving lozenges containing Lactobacillus rhamnosus or Bifidobacterium breve.

    • Purpose: Recolonize the esophagus with beneficial Gram-positive bacteria.

    • Mechanism: Probiotics competitively inhibit pathogenic bacterial adherence, enhance mucin secretion, and produce antimicrobial peptides Wikipedia.

  2. Prebiotic-Rich Diet

    • Description: High intake of inulin and fructooligosaccharides found in chicory, onions, and garlic.

    • Purpose: Promote growth of commensal microbes.

    • Mechanism: Prebiotics serve as fermentable substrates for beneficial bacteria, increasing short-chain fatty acid (SCFA) production that nourishes epithelial cells.

  3. Swallowing Exercises

    • Description: Guided maneuvers (e.g., tongue‐base exercises, effortful swallows).

    • Purpose: Enhance mechanical clearance of retained food and microbes.

    • Mechanism: Increases peristaltic force and bolus clearance, reducing bacterial stasis PMC.

  4. Alkaline Water Irrigation

    • Description: Daily swish and swallow of pH 8.0 filtered water.

    • Purpose: Neutralize local acidity and inhibit acid‐tolerant pathogens.

    • Mechanism: Raises luminal pH, impairing survival of acidophilic bacteria and soothing mucosal inflammation.

  5. Dietary Fiber Supplementation

    • Description: Psyllium husk or wheat dextrin.

    • Purpose: Promote esophageal and gut motility.

    • Mechanism: Bulks luminal contents, stimulating peristalsis and mechanical clearance of microbes.

  6. Mind-Body Stress Reduction

    • Description: Daily 20-minute guided meditation or biofeedback.

    • Purpose: Reduce stress-induced dysmotility.

    • Mechanism: Lowers sympathetic tone; improves esophageal sphincter function and barrier integrity.

  7. Tongue Cleaning

    • Description: Twice-daily tongue scraper use.

    • Purpose: Decrease oral microbial load that can seed the esophagus.

    • Mechanism: Removes biofilm and reduces pathogenic bacterial transfer during swallowing.

  8. Oral Microbiome Re-balancing

    • Description: Chlorhexidine mouthwash for 7 days monthly.

    • Purpose: Temporarily reduce pathogenic oral bacteria.

    • Mechanism: Broad‐spectrum antiseptic action decreasing reservoirs for esophageal colonization.

  9. Esophageal Balloon Dilation (Non-Obstructive)

    • Description: Low-pressure balloon dilation to 12 mm diameter.

    • Purpose: Improve clearance in patients with mild motility disorders.

    • Mechanism: Gently stretches the lower esophageal sphincter to facilitate passage of bolus and bacteria.

  10. Breathing-Technique Training

    • Description: Diaphragmatic breathing exercises.

    • Purpose: Strengthen lower esophageal sphincter tone.

    • Mechanism: Increases crural diaphragm engagement around the esophagus, reducing reflux and microbial overgrowth.

  11. Nasogastric Tube Mucosal Lavage

    • Description: Weekly instillation of sterile saline via NG tube (in hospitalized patients).

    • Purpose: Mechanically cleanse the esophageal lumen.

    • Mechanism: Direct removal of mucus and adherent bacteria from the mucosal surface.

  12. Capsaicin Desensitization

    • Description: Gradual ingestion of low-dose chili pepper extract.

    • Purpose: Desensitize TRPV1 receptors to reduce pain and reflex dysmotility.

    • Mechanism: Repeated TRPV1 activation leads to receptor downregulation and improved motility patterns.

  13. Oral Microbiota Transplant (Experimental)

    • Description: Application of healthy donor saliva onto buccal mucosa.

    • Purpose: Introduce balanced microbial communities.

    • Mechanism: Salivary microbes seed the upper GI tract, potentially normalizing esophageal flora.

  14. Zinc-Lozenge Therapy

    • Description: 15 mg zinc gluconate lozenges TID.

    • Purpose: Support mucosal healing.

    • Mechanism: Zinc is essential for epithelial repair and tight-junction assembly.

  15. Photobiomodulation

    • Description: Low-level laser therapy applied externally to the neck (twice weekly).

    • Purpose: Reduce inflammation and stimulate microcirculation.

    • Mechanism: Light energy modulates cellular activity, promoting anti-inflammatory cytokine release.

  16. Swallow-Triggered Probiotic Capsules

    • Description: Enteric-coated Lactobacillus capsules opening at pH 4.

    • Purpose: Deliver probiotics directly to the lower esophagus.

    • Mechanism: Ensures live bacteria reach target site to re-establish microbial balance.

  17. Citric-Acid Rinse

    • Description: 0.5% citric acid mouth rinse after meals.

    • Purpose: Maintain acidic barrier against pathogens.

    • Mechanism: Temporarily lowers pH to inhibit growth of Gram-negative bacteria.

  18. Functional Electrical Stimulation

    • Description: Transcutaneous electrical stimulation over the esophageal body (experimental).

    • Purpose: Augment weakened peristalsis.

    • Mechanism: Electrical pulses enhance muscle contractions, improving bolus clearance.

  19. Herbal Gargle with Chamomile

    • Description: Warm chamomile tea gargles QID.

    • Purpose: Soothe mucosal irritation and provide mild antimicrobial effect.

    • Mechanism: Chamazulene and apigenin exert anti-inflammatory and antiseptic actions.

  20. Continued Oral Hygiene Education

    • Description: Monthly dental follow-up focusing on flossing, brushing, and tongue care.

    • Purpose: Sustain long-term reduction in oral-to-esophageal microbial seeding.

    • Mechanism: Reinforces behaviors that limit chronic dysbiosis triggers.


Pharmacological Treatments

These ten drugs target dysbiosis-related mechanisms in esophageal disorders.

  1. Proton Pump Inhibitors (PPIs)

    • Class: Irreversible H^+/K^+ ATPase inhibitors

    • Dosage & Time: Omeprazole 20 mg once daily, 30 min before breakfast

    • Purpose: Reduce acid load that favors Gram-negative overgrowth Wikipedia

    • Mechanism: Suppresses gastric acid secretion, raising pH to shift microbial balance

    • Side Effects: Headache, diarrhea, vitamin B12 deficiency with long-term use

  2. H2-Receptor Antagonists

    • Class: Histamine H2-blockers

    • Dosage & Time: Ranitidine 150 mg BID, with or without meals

    • Purpose: Milder acid suppression alternative

    • Mechanism: Blocks histamine-mediated acid secretion, modestly raising gastric pH

    • Side Effects: Dizziness, headache, rare hepatotoxicity

  3. Baclofen

    • Class: GABA_B receptor agonist

    • Dosage & Time: 10 mg TID, before meals

    • Purpose: Decrease transient lower esophageal sphincter relaxations (TLESRs)

    • Mechanism: Enhances inhibitory neurotransmission in the brainstem to reduce reflux events

    • Side Effects: Fatigue, dizziness, nausea

  4. Rifaximin

    • Class: Non-absorbable broad-spectrum antibiotic

    • Dosage & Time: 550 mg BID for 14 days

    • Purpose: Suppress overgrown Gram-negative bacteria Wikipedia

    • Mechanism: Inhibits bacterial RNA polymerase in the gut lumen, indirectly affecting esophageal microbes

    • Side Effects: Nausea, flatulence

  5. Sucralfate

    • Class: Mucosal protective agent

    • Dosage & Time: 1 g QID, 1 hour before meals and at bedtime

    • Purpose: Enhance mucosal barrier repair

    • Mechanism: Forms protective complex over ulcerated mucosa, binds bile salts and pepsin

    • Side Effects: Constipation

  6. Alginate-Antacid Combination

    • Class: Physical barrier agent

    • Dosage & Time: Gaviscon® 10 mL after meals and at bedtime

    • Purpose: Create raft to prevent reflux and limit bacterial ascent

    • Mechanism: Forms viscous gel that floats atop gastric contents, reducing refluxate exposure

    • Side Effects: Bloating

  7. Metoclopramide

    • Class: Dopamine D2 antagonist, prokinetic

    • Dosage & Time: 10 mg TID, before meals

    • Purpose: Improve esophageal and gastric motility

    • Mechanism: Increases acetylcholine release in GI smooth muscle, enhancing peristalsis

    • Side Effects: Extrapyramidal symptoms, tardive dyskinesia with long use

  8. Domperidone

    • Class: Peripheral D2 antagonist

    • Dosage & Time: 10 mg TID, 30 minutes before meals

    • Purpose: Prokinetic with fewer CNS effects

    • Mechanism: Inhibits dopamine receptors in GI tract, increasing motility

    • Side Effects: Dry mouth, abdominal cramps

  9. Budesonide (Topical)

    • Class: Glucocorticoid

    • Dosage & Time: 1 mg BID—swallowed from an inhaler (EoE protocol) Wikipedia

    • Purpose: Treat eosinophilic component of dysbiosis-driven inflammation

    • Mechanism: Local steroid effect reduces eosinophil infiltration and cytokine release

    • Side Effects: Oral candidiasis, dysphonia

  10. Dupilumab

  • Class: IL-4Rα monoclonal antibody

  • Dosage & Time: 300 mg subcutaneously every 2 weeks (EoE only) Wikipedia

  • Purpose: Target type 2 inflammation in eosinophilic esophagitis

  • Mechanism: Blocks IL-4 and IL-13 signaling, reducing eosinophil recruitment and barrier dysfunction

  • Side Effects: Injection-site reactions, conjunctivitis


Dietary Molecular & Herbal Supplements

All supplements listed have evidence of modulating microbiota, supporting barrier health, or reducing inflammation.

  1. Curcumin (500 mg TID)

    • Function: Anti-inflammatory, antimicrobial

    • Mechanism: Inhibits NF-κB and suppresses pathogenic biofilm formation

  2. Quercetin (250 mg BID)

    • Function: Antioxidant, mast-cell stabilizer

    • Mechanism: Reduces histamine release and oxidative stress in mucosa

  3. L-Glutamine (5 g BID)

    • Function: Epithelial fuel

    • Mechanism: Serves as energy source for enterocytes, strengthening tight junctions

  4. Aloe Vera Gel (10 mL QID)

    • Function: Mucosal soothing

    • Mechanism: Polysaccharides promote mucin secretion and inhibit inflammation

  5. Slippery Elm Bark (500 mg TID)

    • Function: Demulcent

    • Mechanism: Forms protective mucilage coating over irritated mucosa

  6. Deglycyrrhizinated Licorice (DGL) (380 mg chewed before meals)

    • Function: Barrier enhancer

    • Mechanism: Stimulates prostaglandin E2 synthesis, increasing mucus production

  7. N-Acetylcysteine (600 mg BID)

    • Function: Antioxidant, mucolytic

    • Mechanism: Disrupts disulfide bonds in mucus and bacterial biofilms

  8. Ginger Extract (250 mg TID)

    • Function: Prokinetic, anti-nausea

    • Mechanism: Activates gastric motility via serotonin receptors

  9. Omega-3 Fish Oil (1,000 mg daily)

    • Function: Anti-inflammatory

    • Mechanism: Shifts eicosanoid balance toward anti-inflammatory mediators

  10. Green Tea Polyphenols (500 mg BID)

    • Function: Antioxidant, antimicrobial

    • Mechanism: Epigallocatechin-3-gallate inhibits bacterial adhesion and cytokine release

  11. Resveratrol (200 mg daily)

    • Function: Anti-inflammatory, modulates microbiota

    • Mechanism: Activates sirtuins, reduces pro-inflammatory cytokines

  12. Berberine (500 mg BID)

    • Function: Antimicrobial, metabolic modulator

    • Mechanism: Disrupts bacterial cell walls, alters gut microbial composition

  13. Magnesium-Hydroxide (400 mg at bedtime)

    • Function: Mild laxative, pH modifier

    • Mechanism: Raises pH temporarily, promotes motility

  14. Vitamin D3 (2,000 IU daily)

    • Function: Immunomodulatory

    • Mechanism: Enhances tight-junction proteins and antimicrobial peptide expression

  15. Mastic Gum (350 mg TID)

    • Function: Antimicrobial, anti-inflammatory

    • Mechanism: Inhibits Helicobacter and gram-negative overgrowth, reduces IL-6


Regenerative & Stem-Cell Drugs

Emerging therapies aiming to restore epithelial integrity and immune balance.

  1. Palifermin (Recombinant KGF)

    • Dosage: 60 µg/kg IV daily for 3 days

    • Function: Stimulates epithelial proliferation

    • Mechanism: Activates keratinocyte growth factor receptor on mucosal cells

  2. Rebamipide

    • Dosage: 100 mg TID

    • Function: Enhances mucus secretion and healing

    • Mechanism: Induces prostaglandin synthesis and growth factor release

  3. Mesenchymal Stem-Cell Exosomes

    • Dosage: Under investigation (animal models)

    • Function: Anti-inflammatory, tissue regeneration

    • Mechanism: Deliver microRNAs that modulate immune responses and promote repair

  4. EGF-Enriched Hydrogels

    • Dosage: Topical endoscopic application

    • Function: Local epithelial regeneration

    • Mechanism: Provides sustained release of epidermal growth factor

  5. Autologous Platelet-Rich Plasma (PRP)

    • Dosage: Endoscopic injection into esophageal submucosa

    • Function: Growth factor delivery for tissue repair

    • Mechanism: Releases PDGF, TGF-β, VEGF to stimulate neovascularization and healing

  6. Thymosin-α1

    • Dosage: 1.6 mg subcutaneously twice weekly

    • Function: Immunomodulatory

    • Mechanism: Enhances T-cell function and epithelial barrier restoration


Surgical Interventions

Reserved for refractory cases or anatomical contributors to dysbiosis.

  1. Nissen Fundoplication

    • Procedure: 360° wrap of gastric fundus around the lower esophageal sphincter (LES).

    • Why: Strengthens LES to prevent reflux and bacterial ascent Wikipedia.

  2. LINX® Magnetic Sphincter Augmentation

    • Procedure: Placement of magnetized beads around the LES laparoscopically.

    • Why: Provides dynamic reflux barrier without altering gastric anatomy.

  3. Partial Posterior Fundoplication (Toupet)

    • Procedure: 270° wrap of fundus posteriorly.

    • Why: Reduces reflux with lower dysphagia risk compared to full wrap.

  4. Endoscopic Radiofrequency Treatment (Stretta)

    • Procedure: Delivery of RF energy to LES muscle endoscopically.

    • Why: Induces fibrosis and improves barrier function without incisions.

  5. Esophageal Myotomy with Dor Fundoplication

    • Procedure: Longitudinal incision of esophageal muscle with anterior 180° wrap.

    • Why: Treats concurrent achalasia; improves clearance and reduces stasis‐induced dysbiosis.


Prevention Strategies

Actions to maintain esophageal microbial balance and barrier health.

  1. Maintain Optimal Oral Hygiene

  2. Avoid Frequent Acidic Beverages

  3. Eat Smaller, More Frequent Meals

  4. Remain Upright for 2 Hours After Eating

  5. Elevate Head of Bed by 15 cm

  6. Limit Alcohol and Tobacco Use

  7. Manage Stress with Relaxation Techniques

  8. Optimize Glycemic Control in Diabetes

  9. Regular Dental and GI Check-ups

  10. Adhere to Prescribed Acid-Suppressive Therapy if Indicated


When to See a Doctor

  • Persistent Heartburn or Regurgitation despite lifestyle changes for > 2 weeks

  • Dysphagia (difficulty swallowing solids or liquids)

  • Unexplained Weight Loss

  • Odynophagia (painful swallowing)

  • Iron-Deficiency Anemia without other cause

  • New-Onset Chest Pain mimicking cardiac origin


Dietary “Do’s” & “Don’ts”

Do Eat:

  • Lean proteins (chicken, fish)

  • High-fiber fruits and vegetables

  • Non-citrus, low-acid juices

  • Whole grains

  • Alkaline water

Avoid:

  • Citrus fruits (oranges, lemons)

  • Tomatoes and tomato-based products

  • Chocolate, mint, caffeine

  • Carbonated beverages

  • Fried and fatty foods

Disclaimer: Each person’s journey is unique, treatment planlife stylefood habithormonal conditionimmune systemchronic disease condition, geological location, weather and previous medical  history is also unique. So always seek the best advice from a qualified medical professional or health care provider before trying any treatments to ensure to find out the best plan for you. This guide is for general information and educational purposes only. Regular check-ups and awareness can help to manage and prevent complications associated with these diseases conditions. If you or someone are suffering from this disease condition bookmark this website or share with someone who might find it useful! Boost your knowledge and stay ahead in your health journey. We always try to ensure that the content is regularly updated to reflect the latest medical research and treatment options. Thank you for giving your valuable time to read the article.

The article is written by Team RxHarun and reviewed by the Rx Editorial Board Members

Last Updated: August 05, 2025.

 

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