RARE DISEASE
Rare Medical Case: 26-Year-Old Man Seeking Infertility Treatment Found With Uterus, Fallopian Tubes Inside Body
Spinal Muscular Atrophy Drugs: Can Medicine for Rare Disorder SMA Be Made Available at Lower Price in India, Supreme Court to Drug Manufacturer
Guillain-Barré Syndrome Scare: 5 New GBS Cases Detected in Pune, Tally Up at 163 in Maharashtra
Guillain-Barre Syndrome in Maharashtra: Suspected GBS Deaths Rise to 4, Case Tally at 140; E Coli Found in Water Sample
Guillain-Barre Syndrome in Maharashtra: Man Suspected To Have Contracted GBS Dies in Solapur; Cases Top 100 in Pune
Guillain-Barre Syndrome in Pune: 64 Cases of GBS Detects in City, 13 Patients on Ventilators
Guillain-Barre Syndrome in Pune: Maharashtra Reports First Death of Rare Disease GBS in DSK Vishwa Area
Rajasthan: Twins Born in Bikaner's Nokha Town With Plastic-Like Skin, Suffer From Genetic Disorder Called Harlequin-Type Ichthyosis
Rare Disease Treatment Amount Hiked: Centre To Give Up to INR 50 Lakh per Patient for Treatment of Rare Diseases, Says Union Minister Anupriya Singh Patel
‘Bleeding Eyes’ Disease Claims Life in Spain: Man Dies by ‘Ebola-Like’ Virus After Getting Bitten by Tick
What Is Rare Sensory Neural Nerve Hearing Loss? From Symptoms to Treatment, Know All About Sensorineural Nerve Disorder Indian Playback Singer Alka Yagnik Has Been Diagnosed With
Rare Disease Day 2024 Date, History and Significance: Know About the Event Observed on the Last Day of February To Raise Awareness for Rare Diseases
Karnataka CM Siddaramaiah Writes to PM Narendra Modi Requesting Waiver of Import Taxes on Zolgensma Injection to Treat Baby Battling Rare Disease
Haryana Health Minister Anil Vij Provides Financial Help to Boy Suffering From Rare Disease Aplastic Anemia
US: Woman Dies of Severe Malnutrition After Carrying Rare ‘Stone Baby’ Inside Her For Nine Years
Health Ministry Asks Eight Hospitals to Set Up Committees to Decide on Applications For Aid to Treat Rare Diseases Like Thalassemia And Haemophilia
What is Fibrodysplasia Ossificans Progressiva? Five-Month-Old Baby Girl From UK ‘Turning to Stone’ as She Suffers From Rare Genetic Condition, FOP
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