SCID-AI · 405 SNS Axis Business Space, Nanpura, Surat
Mon–Sat: 11–1 PM & 4–6 PM
TB Specialist Surat — SCID-AI DOTS GeneXpert
Tuberculosis in India 2.8M New TB cases in India every year — highest burden globally
 TB Specialist · SCID-AI, Surat · GeneXpert · DOTS

TuberculosisSpecialist — Surat

SCID-AI provides complete TB care — GeneXpert diagnosis, DOTS supervision, drug-sensitive and drug-resistant TB management, HIV-TB co-infection, extrapulmonary TB, and isoniazid preventive therapy. Dr. Pratik Savaj, FNB Infectious Diseases, has specific training in complex TB from P.D. Hinduja Hospital, Mumbai.

GeneXpert First-Line DOTS Supervision MDR-TB & XDR-TB HIV-TB Co-Infection Extrapulmonary TB
Understanding Tuberculosis

What Is Tuberculosis — and Why Does It Need a Specialist?

Tuberculosis is caused by Mycobacterium tuberculosis — a slow-growing bacterium that primarily infects the lungs but can affect virtually any organ. It spreads through the air when a person with active pulmonary TB coughs, sneezes, or speaks — releasing microscopic droplet nuclei that can remain suspended in the air for hours.

TB is uniquely complex for three reasons. First, it is slow — the bacterium divides every 20–24 hours (most bacteria divide in 20–30 minutes), which is why treatment takes months, not days. Second, it hides — latent TB infection allows the bacterium to persist dormant in the body for decades before reactivating. Third, it develops drug resistance when treatment is inadequate, creating strains that are far harder and more expensive to treat.

India has the world’s highest TB burden — 2.8 million new cases per year. TB is curable with the right diagnosis, the right drugs, and completion of the full course. Specialist care matters most when standard approaches have failed, when drug resistance is present, or when TB affects organs outside the lungs.

Why TB Needs a Specialist

Drug resistance: MDR-TB and XDR-TB require specialist regimen design — standard DOTS drugs will fail
Extrapulmonary TB: TB outside the lungs is frequently missed — normal chest X-ray does not rule out TB
HIV co-infection: Integrated HIV-TB management requires expertise spanning two complex specialities
Treatment failure: Positive sputum at 2 months is a specialist-level diagnostic problem requiring culture + DST
Tuberculosis specialist SCID-AI Surat

Key TB Facts

CauseMycobacterium tuberculosis
SpreadAirborne droplet nuclei
India burden2.8M new cases/year
DS-TB treatment6 months HRZE+HR
Cure rate (DS-TB)95%+ with full course
TB Symptoms

TB Symptoms — When to See a Specialist

TB symptoms develop slowly over weeks to months — not suddenly like dengue or malaria. This gradual onset is one reason TB is frequently diagnosed late. The constitutional symptoms (fever, night sweats, weight loss) occur in both pulmonary and extrapulmonary forms.

Pulmonary TB

Cough 2+ weeks — the cardinal symptom
Haemoptysis (coughing blood)
Chest pain on breathing
Shortness of breath
Low-grade fever, typically afternoon

Constitutional Symptoms

Unexplained weight loss — 5–10 kg over months
Persistent fever — weeks to months
Night sweats — drenching, requiring clothes change
Profound fatigue, loss of appetite
Swollen lymph nodes — painless, rubbery

Extrapulmonary TB — No Cough, Normal Chest X-Ray

Lymph node TB: Painless neck swelling for weeks
Spinal TB: Back pain, leg weakness, numbness
TB Meningitis: Headache, neck stiffness, fever
Abdominal TB: Chronic pain, ascites
Renal TB: Flank pain, sterile pyuria
TB Pericarditis: Chest pain, breathlessness

See Dr. Savaj If

Cough lasting more than 2 weeks; unexplained weight loss with fever; any persistent swollen lymph nodes; fever of unknown origin; back pain with neurological signs; or any fever in an HIV-positive patient. In Surat’s endemic setting, TB must be actively excluded — not passively assumed absent.

TB symptoms assessment SCID-AI Surat

High-Risk Groups in Surat

HIV-positive individuals — 20× higher TB risk
Household contacts of active TB cases
Diabetic patients — significantly elevated risk
Workers in high-density settings — textiles, construction
Immunocompromised — steroids, chemotherapy, TNF inhibitors
Children under 5 in TB-contact households
Malnourished individuals — impaired immune containment
TB Prevention

How to Prevent Tuberculosis

TB prevention operates at three levels: preventing exposure, preventing progression from latent to active TB, and preventing transmission from active cases to contacts. Each level has specific evidence-based interventions.

BCG Vaccination at Birth

BCG is given to all newborns under India’s Universal Immunisation Programme. It provides strong protection against severe childhood TB forms — TB meningitis and miliary TB. All children should receive BCG within 24 hours of birth.

Isoniazid Preventive Therapy (IPT)

6 months of daily isoniazid for high-risk contacts with latent TB. Recommended for: all HIV-positive patients (after excluding active TB), children under 5 who are household contacts, and immunocompromised individuals with positive IGRA/TST. Reduces reactivation risk by 60–90%.

Respiratory Precautions for Active TB Patients

Patients with active pulmonary TB should wear a surgical mask around others until sputum converts negative on treatment; ensure adequate natural ventilation; avoid crowded enclosed spaces; and not share sleeping spaces with children or immunocompromised people during the infectious period.

Contact Investigation and Screening

Every household contact of a TB patient should be evaluated — not just symptomatic ones. Children under 5 and immunocompromised contacts are priority. IGRA/TST identifies latent TB. GeneXpert and CXR exclude active TB. SCID-AI includes all household members in contact assessment.

ART for HIV-Positive Individuals

HIV-positive individuals are 20 times more likely to develop active TB. ART reduces TB risk by 60–65% by restoring immune function. Combined ART + IPT is the most powerful TB prevention strategy for HIV-positive individuals.

Complete TB Treatment — Prevent Drug Resistance

Every patient who starts TB treatment must complete the full course. Stopping early allows surviving bacteria to develop resistance and infect others. Completing TB treatment is an act of community prevention, not just personal treatment.

TB prevention BCG vaccination SCID-AI Surat

Free TB Prevention in India

India’s NTEP provides: free BCG for all newborns; free isoniazid for preventive therapy; free IGRA testing at designated centres; and free contact investigation for household contacts. Dr. Savaj coordinates with NTEP for eligible patients.

Forms of TB

Forms of Tuberculosis Treated at SCID-AI

TB is not a single condition — it is a family of diseases caused by Mycobacterium tuberculosis affecting different organs, with different presentations, different diagnostic approaches, and in the case of drug-resistant forms, completely different treatment regimens.

TB Can Occur Without a Cough

Extrapulmonary TB — TB affecting lymph nodes, spine, abdomen, brain, kidneys — presents with no respiratory symptoms and a normal chest X-ray. This is why many extrapulmonary TB cases are diagnosed late. At SCID-AI, TB is actively considered in any patient with persistent unexplained fever, swollen glands, or organ-specific symptoms — regardless of chest findings.

Pulmonary TB

Lung involvement — most common form

Cough >2 weeks, haemoptysis, fever, night sweats, weight loss. Diagnosed by GeneXpert + sputum culture + chest X-ray. Treated with 6-month HRZE+HR regimen under DOTS supervision.

Extrapulmonary TB

Lymph node, spine, brain, abdomen

Lymph node TB (most common): painless swelling. Spinal TB (Pott’s): back pain + neurological signs. Meningeal TB: headache + neck stiffness. Treatment 9–12 months. Requires biopsy/culture for diagnosis.

Latent TB Infection

Infected but not ill — no symptoms

TST or IGRA positive but no active disease. Asymptomatic and not infectious. Risk of reactivation: 5–10% lifetime. Higher with HIV, diabetes, immunosuppression. Treated with isoniazid preventive therapy (IPT) 6 months.

MDR-TB

Resistant to isoniazid + rifampicin

Caused by inadequate prior treatment or transmission of resistant strain. Requires 18–24 months of second-line drugs: bedaquiline, linezolid, clofazimine, moxifloxacin. Intensive specialist monitoring essential.

Pre-XDR & XDR-TB

Additional resistance — most complex

Pre-XDR: MDR + fluoroquinolone resistant. XDR: additionally resistant to bedaquiline or linezolid. Extremely limited treatment options. Requires specialist team at a designated XDR-TB centre. Dr. Savaj manages and refers appropriately.

HIV-TB Co-Infection

Requires integrated specialist management

HIV doubles TB risk 20-fold. TB is the leading cause of HIV-related death. Integrated management of both — ART timing, drug interactions (rifampicin+efavirenz), IRIS management — is a core SCID-AI specialty.
TB Diagnosis at SCID-AI

How TB Is Diagnosed — GeneXpert First, Always

1

GeneXpert MTB/RIF — First-Line Test

Always before starting treatment

GeneXpert simultaneously detects Mycobacterium tuberculosis and rifampicin resistance in 2 hours from a single sputum sample. Sensitivity 85–90% — far higher than sputum smear (50–60%). Rifampicin resistance on GeneXpert = highly predictive of MDR-TB, requiring immediate management change. At SCID-AI, GeneXpert is not an add-on after smear negativity — it is the first-line diagnostic for all suspected TB cases.

2

Sputum Culture + Drug Sensitivity Testing (DST)

Gold standard — 4–8 weeks

MGIT liquid culture (4–8 weeks) grows the organism and allows comprehensive drug sensitivity testing against all first and second-line drugs. Essential for: confirming MDR-TB suspected on GeneXpert; guiding second-line regimen selection for MDR/XDR-TB; and resolving discordant GeneXpert results. Culture also confirms diagnosis when GeneXpert is negative in strong clinical suspicion.

3

Chest X-Ray + HRCT Thorax

Anatomical extent of disease

Chest X-ray provides immediate visual assessment of lung involvement. HRCT (high-resolution CT) thorax gives more detail — cavities, nodules, tree-in-bud pattern — useful in sputum-negative cases, assessing extent of disease, and monitoring treatment response. Important: a normal chest X-ray does not rule out TB — extrapulmonary TB has no lung findings.

4

IGRA / Tuberculin Skin Test (TST)

Latent TB diagnosis

Interferon-gamma release assay (IGRA) — a blood test — or TST detects immune sensitisation to TB antigens, indicating latent TB infection. Used for: contact investigation of TB cases, screening of HIV patients for preventive therapy, and assessing immunocompromised patients before immunosuppressive drugs. IGRA is more specific than TST in BCG-vaccinated individuals (which is virtually everyone in India).

5

Biopsy + Histopathology (Extrapulmonary TB)

Essential for extrapulmonary forms

For lymph node, pleural, pericardial, abdominal, or tissue TB — tissue biopsy with GeneXpert on the specimen and histopathology showing caseating granulomas is the diagnostic approach. Fine needle aspiration cytology (FNAC) of enlarged lymph nodes, guided by ultrasound, provides tissue without open surgery. This is often the only way to diagnose extrapulmonary TB that has been missed by chest-focused investigations.

6

HIV Test — Mandatory in All TB Patients

Non-negotiable at SCID-AI

Every TB patient at SCID-AI is offered and recommended HIV testing. HIV status fundamentally changes TB management: ART timing, drug selection, IRIS risk, IPT for contacts. Missing HIV in a TB patient means managing TB without the most important prognostic co-factor. Fully confidential under HIV Act 2017.

TB GeneXpert diagnosis SCID-AI Surat

 Don’t Start Antibiotics Before Testing

A single dose of rifampicin or fluoroquinolones can sterilise a sputum sample and produce a false-negative GeneXpert. Always collect sputum for GeneXpert before starting any antibiotic — including broad-spectrum drugs like levofloxacin, moxifloxacin, or azithromycin.

Sputum before rifampicin — always
Avoid fluoroquinolones empirically if TB is suspected
Two sputum samples: one early morning, one spot
Bring previous reports to your first visit
 Book TB Assessment
TB Treatment

How TB Is Treated — DOTS, Regimens, and Duration

TB treatment is antibiotic therapy — but the specifics matter enormously. The right drugs, the right doses, for the full duration, under DOTS supervision (to ensure every dose is taken) are the pillars of treatment success. Inadequate treatment drives drug resistance.

 Drug-Sensitive TB (DS-TB) — Standard Treatment
2 months HRZE
4 months HR (continuation)
 H=Isoniazid  R=Rifampicin  Z=Pyrazinamide  E=Ethambutol
 Intensive phase kills majority of bacteria; continuation phase eliminates persisting organisms
 Treatment success rate: 95%+ with full course completion under DOTS
 Never stop early — even when feeling better. Incomplete treatment causes relapse and resistance.
 Extrapulmonary TB (Spinal / Meningeal) — Extended Treatment
2m HRZE
7–10 months HR (continuation)
 Extended continuation phase needed for CNS and spinal TB due to poor drug penetration into CSF and bone
 Corticosteroids (dexamethasone) added for TB meningitis and pericarditis to reduce inflammatory damage
 Spinal TB: immobilisation, physiotherapy, and sometimes surgical decompression for cord compression
 MDR-TB — Second-Line Regimen (BPaLM / BDQ-based)
6 months intensive
12–18 months continuation (total 18–24m)
 BPaLM: Bedaquiline + Pretomanid + Linezolid + Moxifloxacin — WHO-recommended shorter MDR-TB regimen (6–9 months for eligible patients)
 Cardiac monitoring (QTc) required for bedaquiline + moxifloxacin (both prolong QT interval)
 Monthly sputum culture during treatment to confirm conversion to negative
 MDR-TB drugs available free through NTEP; Dr. Savaj coordinates with NTEP when required

DOTS — Why Every Dose Must Be Supervised

Directly Observed Treatment Short-course (DOTS) means a trained healthcare worker watches the patient swallow every dose. This is not punitive — it is the evidence-based standard that prevents drug resistance. When patients take TB drugs inconsistently or stop early, surviving bacteria develop resistance. DOTS eliminates this risk. At SCID-AI, Dr. Savaj supervises DOTS or coordinates with NTEP DOTS centres for all TB patients.

TB treatment DOTS HRZE pills SCID-AI
Drug-Resistant Tuberculosis

MDR-TB & XDR-TB — When Standard Treatment Fails

Drug-resistant TB is India’s most urgent TB crisis. India has the world’s largest MDR-TB burden — over 130,000 new cases per year. MDR-TB develops when drug-sensitive TB is treated with wrong drugs, wrong doses, interrupted treatment, or poor-quality medications. Once drug resistance develops, treatment becomes vastly more complex, more toxic, more prolonged, and less successful.

At SCID-AI, Dr. Savaj has specific training in MDR-TB management from his fellowship at P.D. Hinduja Hospital — one of India’s principal MDR-TB centres. He manages culture-confirmed MDR-TB with individualised regimens based on DST, coordinates free NTEP second-line drugs, and provides monthly monitoring of treatment response and drug toxicity.

 Book MDR-TB Consultation
Resistance TypeDrugs Resistant ToTreatmentSuccess Rate
Drug-Sensitive (DS-TB)Sensitive to allHRZE × 2 + HR × 495%+
Isoniazid-Resistant (Hr-TB)Isoniazid onlyRZE + fluoroquinolone × 6m85–90%
MDR-TBIsoniazid + RifampicinBPaLM or BDQ-based × 18–24m55–65%
Pre-XDR-TBMDR + FluoroquinoloneIndividualised × 20–24m40–55%
XDR-TBPre-XDR + BDQ or LZDIndividualised specialist team<40% — specialist centre

Warning Signs of MDR-TB

Sputum still positive after 2 months of treatment
GeneXpert shows rifampicin resistance
Symptoms returning or worsening on treatment
Prior TB treatment that was incomplete or interrupted
Close contact with a confirmed MDR-TB patient
TB Services at SCID-AI

Complete TB Care — All Under One Roof

GeneXpert-First Diagnosis

GeneXpert MTB/RIF as the first-line test for all suspected TB — not an add-on after smear negativity. Same-day rifampicin resistance detection. Sputum culture + full DST for all cases. Extrapulmonary biopsy coordination.

DOTS Supervision

Directly Observed Treatment for all drug-sensitive TB. Dr. Savaj is a private DOTS provider or coordinates with NTEP DOTS centres. Monthly sputum monitoring during treatment. Free NTEP drugs coordinated for eligible patients.

MDR-TB & XDR-TB Management

Specific training from P.D. Hinduja Hospital. Culture-confirmed MDR-TB managed with DST-guided second-line regimens including bedaquiline-based BPaLM. Monthly culture monitoring, cardiac QTc monitoring, drug toxicity management.

HIV-TB Co-Infection

Integrated HIV-TB management: ART timing (2 weeks if CD4 <50), drug interaction management (rifampicin+dolutegravir/efavirenz), IRIS recognition and management, and isoniazid preventive therapy for HIV contacts.

Contact Investigation & IPT

Household contact evaluation, IGRA/TST for latent TB detection. Isoniazid preventive therapy (6 months) for contacts with latent TB — especially children under 5 and immunocompromised household members. Reduces reactivation risk by 60–90%.

Extrapulmonary TB Diagnosis

Lymph node, spinal, meningeal, abdominal, pleural, and renal TB. Tissue biopsy coordination, GeneXpert on biopsy specimens, CSF analysis for TB meningitis, and prolonged 9–12 month treatment protocols.

TB specialist services SCID-AI Surat
HIV-TB co-infection management SCID-AI
TB-HIV Co-Infection

Why TB and HIV Must Be Managed Together

20×Higher TB risk with HIVImmune suppression effect
#1TB: leading HIV-related cause of deathGlobally
2 wksART starts after TB treatment (CD4<50)Critical timing window
All TBpatients need HIV testingSCID-AI policy — non-negotiable

HIV suppresses the CD4 T-cells that contain latent TB. This makes HIV-positive individuals 20 times more likely to develop active TB. TB in turn accelerates HIV by triggering immune activation and increasing viral replication. Managing one without the other produces consistently inferior outcomes.

ART timing: Start TB treatment first. Start ART within 2 weeks if CD4 <50. Within 8 weeks if CD4 >50.
Drug interactions: Rifampicin induces CYP450 — reduces levels of many ARTs. Use dolutegravir (double dose) or adjusted efavirenz. Never nevirapine with rifampicin.
TB-IRIS: Immune reconstitution inflammatory syndrome — TB symptoms worsen paradoxically after ART starts. Recognised and managed at SCID-AI without stopping ART unnecessarily.
IPT: All HIV-positive patients without active TB should receive 6 months of isoniazid preventive therapy after excluding active disease.
MDR-TB in HIV: Double complexity — drug interactions between second-line TB drugs and ART require specialist management.

Every TB Patient at SCID-AI Is Offered HIV Testing

This is a non-negotiable clinical standard at SCID-AI — not optional. HIV status changes every aspect of TB management: ART timing, drug selection, monitoring, IPT for contacts, and prognosis. All HIV testing is fully confidential under HIV Act 2017.

Patient Reviews

What TB Patients Say About SCID-AI

My TB was not responding to the standard DOTS treatment. Dr. Savaj sent a sputum culture and DST. Found rifampicin resistance — MDR-TB. He changed my treatment to a bedaquiline-based regimen. Six months later, my sputum culture converted to negative. He literally saved my life.

SK
Salim K.MDR-TB · Surat

My wife had TB and Dr. Savaj tested me and both my children. I had latent TB (IGRA positive). He put me on isoniazid preventive therapy for 6 months. My younger child was under 5 — he said this was the most important person to treat. One year on, we are all well. Thorough and caring.

PD
Prashant D.Latent TB / Contact · Surat
Common TB Questions

Frequently Asked Questions About TB

Answered by Dr. Pratik Savaj, FNB Infectious Diseases, SCID-AI, Surat.

What is GeneXpert and why is it better than sputum smear?
GeneXpert MTB/RIF (Xpert) is a rapid molecular test that simultaneously detects TB (Mycobacterium tuberculosis) and rifampicin resistance in 2 hours. Sputum smear microscopy — the traditional test — detects only 50–60% of TB cases and cannot detect drug resistance. GeneXpert detects 85–90% of TB cases, works with a single sputum sample, and immediately flags rifampicin resistance (the key indicator of MDR-TB). At SCID-AI, GeneXpert is the first-line test for all suspected TB cases — not an add-on after smear negativity.
How long does TB treatment take?
Treatment duration depends on the type of TB. Drug-sensitive TB (DS-TB): 6 months — 2 months intensive phase (HRZE) + 4 months continuation phase (HR). Extrapulmonary TB (spinal, meningeal): 9–12 months. MDR-TB: 18–24 months with second-line drugs including bedaquiline-based regimens. XDR-TB and Pre-XDR-TB: individualized, often 24+ months. Stopping TB treatment early — even when you feel better — causes relapse and drives drug resistance. Complete the full course.
What is MDR-TB and how is it different from normal TB?
MDR-TB is tuberculosis caused by a strain of Mycobacterium tuberculosis that is resistant to at least isoniazid and rifampicin — the two most powerful first-line TB drugs. This resistance develops when TB is treated inadequately — wrong drugs, wrong doses, interrupted treatment, or poor-quality medications. MDR-TB requires second-line drugs (fluoroquinolones, bedaquiline, linezolid, clofazimine) for 18–24 months. These drugs are more toxic, more expensive, and require far more intensive monitoring. XDR-TB (Extensively Drug-Resistant TB) is additionally resistant to fluoroquinolones and at least one injectable — leaving very limited treatment options.
Can TB be completely cured?
Yes — drug-sensitive TB is fully curable in 95%+ of patients who complete the full 6-month treatment course. Even MDR-TB has treatment success rates of 55–65% with appropriate second-line regimens and specialist monitoring. The key requirements for cure: correct drugs based on sensitivity testing, full course completion without interruption, adequate nutrition and supportive care, and regular monitoring to detect and manage side effects and treatment failure. At SCID-AI, Dr. Savaj manages every case with these requirements as non-negotiable.
Is free TB treatment available in Surat?
Yes. All TB treatment is free under India’s National Tuberculosis Elimination Programme (NTEP) through government DOTS centres — including first-line drugs for DS-TB and second-line drugs for MDR-TB. Free GeneXpert testing is available at NTEP-enrolled labs. SCID-AI coordinates with NTEP where appropriate — Dr. Savaj can initiate DOTS under private DOTS provider status or refer to the nearest government DOTS centre. For patients who prefer private management, the same drugs are available at pharmacies at modest cost. Dr. Savaj advises patients on the best pathway for their specific situation.
Do household contacts of a TB patient need to be tested?
Yes — contact investigation is a critical and commonly neglected step in TB management. All household contacts of a confirmed TB patient should be assessed. Children under 5 years and immunocompromised contacts (HIV-positive, diabetic, on steroids) are at highest risk of developing active TB after exposure and need priority assessment. Contacts with positive tuberculin skin test (TST) or IGRA but no active disease may benefit from isoniazid preventive therapy (IPT) —6 months of isoniazid to prevent progression to active TB. Dr. Savaj provides contact tracing guidance and IPT where indicated.
Can I have TB without a cough or chest symptoms?
Yes. Extrapulmonary TB can occur without any respiratory symptoms. TB can affect the lymph nodes (most common extrapulmonary site — presenting as persistent neck or axillary swelling), spine (Pott’s disease — back pain, weakness), meninges (headache, fever, neck stiffness), abdomen (pain, ascites), kidneys (sterile pyuria), and other organs. A normal chest X-ray does not rule out TB. Many patients with extrapulmonary TB have been seen by multiple specialists without a diagnosis because the possibility of TB wasn’t considered. If you have persistent unexplained symptoms — particularly in India where TB is endemic — TB must be systematically excluded.
What is the difference between latent TB and active TB?
Latent TB: The TB bacteria are present in the body (positive TST or IGRA) but contained by the immune system — not replicating, not causing symptoms, not infectious. About 25% of the world’s population has latent TB. Latent TB cannot be diagnosed by sputum test or chest X-ray — only by TST or IGRA. Active TB: The immune system has lost control and TB bacteria are actively replicating — causing symptoms and potentially infectious. Latent TB reactivates into active TB in about 5–10% of cases over a lifetime — risk is much higher with HIV, diabetes, immunosuppression, or malnutrition. Isoniazid preventive therapy (IPT) reduces reactivation risk by 60–90%.
Consult Dr. Pratik Savaj

Suspected TB? Get the Right Diagnosis First.

No referral needed. Dr. Pratik Savaj, FNB Infectious Diseases, provides GeneXpert-first TB diagnosis, DOTS supervision, MDR-TB management, and HIV-TB co-infection care at SCID-AI, Nanpura, Surat. The right diagnosis before the first antibiotic changes everything.

SCID-AI, Nanpura, Surat — 405 SNS Axis Business Space, Besides Mahavir Hospital, Surat 395001
Mon–Sat: 11 AM–1 PM & 4–6 PM · Sunday: Closed
+91 72839 34807 — Call or WhatsApp
Dr. Pratik Savaj
Dr. Pratik Savaj FNB Infectious Diseases
MBBS · DNB Medicine · Fellowship ID
P.D. Hinduja Hospital, Mumbai
Morning11:00 AM – 1:00 PM, Mon–Sat
Evening4:00 PM – 6:00 PM, Mon–Sat
Phone+91 72839 34807
 WhatsApp to Book