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Best Anemia Treatment doctors in Safdarjung Development Area

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Dr. Rommel Tickoo Anemia Treatment

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Dr. Anamika Dubey Anemia Treatment

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Dr. Monica Mahajan Anemia Treatment

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Dr. Sunil Nigam Anemia Treatment

Dr. Sunil Nigam

Internal Medicine

50 years of experience

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Dr. Rajkumar Karwani Anemia Treatment

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Dr. Gita Prakash Anemia Treatment

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Dr. Anupama Singh Anemia Treatment

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Dr. M.l.kalra Anemia Treatment

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Dr. Tribhuvan Gulati Anemia Treatment

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Dr. Tanya Bhardwaj Anemia Treatment

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Top 10 Anemia Treatment doctors Near Safdarjung Development Area

Doctor RatingExperienceFee
Dr. Rommel Tickoo

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29₹ 1500
Dr. Anamika Dubey

1

30₹ 1100
Dr. Monica Mahajan

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32₹ 1000
Dr. Sunil Nigam

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50₹ 1000
Dr. Rajkumar Karwani

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32₹ 600
Dr. Gita Prakash

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47₹ 600
Dr. Anupama Singh

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26₹ 1200
Dr. M.l.kalra

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43₹ 1000
Dr. Tribhuvan Gulati

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21₹ 400
Dr. Tanya Bhardwaj

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4 ₹ 500

Questions & Answers on "Anemia Treatment" (275)

Dear Doctor, Due to my father's high blood viscosity, suspicion of polycythemia arises, necessitating blood draws every 3 weeks to maintain appropriate levels. At 69 years old, he experiences symptoms such as skin itching, swelling, head numbness, and fatigue. Currently, his JAK2 V617F mutation showed 0.8 then 1.2%, with JAK2 exon 12 negative and EPO at 13.4. Abdominal CT and chest X-ray are normal. After a few months of phlebotomy, his levels normalized. Now, we await the bone marrow biopsy results, which do not confirm Polycythemia Vera: "Microscopic description: The bone marrow biopsy sample shows somewhat hypocellular hematopoietic parenchyma relative to age, which is terminally mature. Myeloid ratio is 2:1 with dominance of late precursors; no blast cells are noted. The number of megakaryocytes is normal with no clustering. There is no interstitial fibrosis or lymphoid infiltrate. Diagnosis: Mature, hypocellular hematopoietic parenchyma without myeloproliferative features. Cytogenetic analysis confirmed male karyotype; no clonal chromosomal abnormalities detected. Indication for examination D7510 Secondary polycythemia Note Submicroscopic rearrangements, small structural chromosomal aberrations, DNA-level differences cannot be ruled out with the method used." I am quite confused as JAK2 positivity typically suggests PV, yet the biopsy suggests otherwise, possibly indicating secondary polycythemia. Could you please clarify based on this information what you personally think is more likely, Polycythemia Vera or another secondary cause? Thank you very much for your help.

Male | 67

Your father's symptoms and test results do suggest some complexity. The presence of JAK2 mutation often points towards Polycythemia Vera (PV), but the bone marrow biopsy does not show typical myeloproliferative features, suggesting it might be secondary polycythemia instead. Consult a hematologist, specializing in blood disorders, and can provide a more accurate diagnosis and appropriate treatment plan.

 

Answered on 3rd July '24

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আমার হাতের আঙ্গুল দিয়ে একাকাই রক্ত পড়ছে। আমি তার জন্য একটা টিটেনাস নিয়েছি কিন্ত এখনও রক্ত পড়ছে। এখন আমি কি করব বুঝতে পারছি না।

Male | 15 Year

রক্ত পড়া সাধারণত আঘাতের কারণে হয়, যা সংক্রমণ বা অন্যান্য সমস্যার জন্য সংকেত হতে পারে। প্রথমে আঘাতটি পরিষ্কার করুন এবং একটি বিকল্প ব্যান্ডেজ ব্যবহার করে পুরোপুরি চাপ দিন। যদি রক্তপাত বন্ধ না হয় বা এটি বেড়ে যায়, তাহলে দ্রুত ডাক্তারের সঙ্গে যোগাযোগ করা উচিত। টিটেনাস প্রাপ্তি গুরুত্বপূর্ণ, কিন্তু যদি আপনার আঘাত গভীর হয় বা অন্য কোনো সমস্যা অনুভব করেন, তাহলে পেশাদার চিকিৎসা সেবা গ্রহণ করা আপনার জন্য নিরাপদ। মনে রাখবেন, সঠিক চিকিৎসা পাওয়া গুরুত্বপূর্ণ। আপনি চিন্তা করবেন না, অধিকাংশ আঘাত ভালোভাবে মেরামত হয়।

Answered on 25th Mar '25

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