Rare Genetic Condition
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How Scientists Changed Their View Of Insomnia
- Friday April 24, 2026
- Health | Iuliana Hartescu, The Conversation
Insomnia rarely occurs on its own, which brings us to one of the biggest changes scientists have made in our understanding of chronic sleep deprivation.
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www.ndtv.com
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Six Real Genetic Mutations That Sound Like Superpowers
- Friday April 3, 2026
- Science | Edited by Nikhil Pandey
Scientists have identified rare genetic mutations granting extraordinary abilities, including minimal sleep, extreme strength, and reduced fear or pain responses.
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www.ndtv.com
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Doctors Express Concern Over Child Diagnosed With Chronic Disease Typically Seen In Adults
- Wednesday April 1, 2026
- Health | Press Trust of India
Doctors in a Delhi NCR hospital have reported a rare case of chronic pancreatitis in a 10-year-old girl, a condition typically associated with prolonged alcohol and tobacco use in adults, raising concern among specialists.
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www.ndtv.com
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Catherine O'Hara Lived With Situs Inversus. What The Genetic Organ-Placement Condition Means
- Saturday January 31, 2026
- Lifestyle | Written by Krati Purwar
"I am a freak," said Catherine O'Hara, laughing about the genetic condition in which her organs were flipped
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www.ndtv.com/lifestyle
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Stranger Things Star Gaten Matarazzo Was Born With Cleidocranial Dysplasia, Know About The Rare Genetic Condition
- Thursday January 1, 2026
- Lifestyle | Written by Krati Purwar
Stranger Things star Gaten Matarazzo was born without collarbones, and the rare genetic condition has affected his teeth and height
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www.ndtv.com/lifestyle
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The Invisible Disorder: An Indian Mother Shares How An Ultra-Rare Genetic Disease Reshaped Her Family's Life
- Thursday December 11, 2025
- Health | Written by Shreya Goswami
Norrie Disease is an ultra-rare genetic disorder causing congenital blindness, progressive hearing loss and neurological challenges. One Indian mother's journey reveals how misunderstood the condition is, and why early genetic screening and awareness
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www.ndtv.com
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Did Adolf Hitler Really Have A Micropenis? Rare Genetic Disorder Kallmann Syndrome Explained
- Saturday November 15, 2025
- Health | Written by Shreya Goswami
Kallmann Syndrome is a rare genetic disorder that causes delayed puberty and a poor sense of smell. New DNA findings suggest Adolf Hitler may have had features of this condition.
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www.ndtv.com
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Rare Orange Shark Spotted In Costa Rica, Experts Reveal Reason Behind Its Bright Colour
- Wednesday August 27, 2025
- Offbeat | Edited by Srishti Singh Sisodia
More research is needed to explore potential genetic or environmental factors influencing this rare pigmentation anomaly in sharks.
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www.ndtv.com
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Indian-Origin Man Claims London Cafe Refused Him Service Because Of His Face: "Everyone Was Staring At Me"
- Sunday May 18, 2025
- World News | Edited by Ritu Singh
He described the experience as distressing, saying that everyone in the cafe was staring at him, making him feel like a "ghost".
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www.ndtv.com
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"Everyone Is A Cousin" In This Village. Courtesy: A Rare Genetic Condition
- Monday May 12, 2025
- World News | Edited by NDTV News Desk
A small village in Brazil is afflicted with Spoan syndrome, a rare hereditary illness that weakens the body over time by affecting the nervous system.
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www.ndtv.com
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Model Katie Price "Heartbroken" Over Son Harvey's Health, Says He's At Risk Of Heart Attack
- Monday April 21, 2025
- Feature | Edited by Anjali Thakur
Harvey, who lives with a rare genetic condition called Prader-Willi syndrome, now weighs close to 30 stone (around 188 kg).
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www.ndtv.com
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Olivia Farnsworth: UK Girl Who Feels No Pain, Hunger, Or Fatigue
- Thursday March 13, 2025
- World News | Edited by Nikhil Pandey
Olivia Farnsworth, a UK girl, has a rare genetic condition that makes her insensitive to pain, hunger, and fatigue, posing significant health risks and requiring constant monitoring and management to ensure her well-being.
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www.ndtv.com
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17,000-Year-Old DNA of Ice Age Infant Reveals Dark Skin, Blue Eyes
- Monday October 28, 2024
- Written by Gadgets 360 Staff
Analysis of a 17,000-year-old infant’s remains from southern Italy sheds light on Ice Age ancestry and health. The infant, found in a Puglian cave, was likely around a year old at death and had distinctive traits—brown skin, blue eyes, and curly dark hair. His genome links him to Europe’s Villabruna lineage, suggesting their presence in south...
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www.gadgets360.com
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How Scientists Changed Their View Of Insomnia
- Friday April 24, 2026
- Health | Iuliana Hartescu, The Conversation
Insomnia rarely occurs on its own, which brings us to one of the biggest changes scientists have made in our understanding of chronic sleep deprivation.
-
www.ndtv.com
-
Six Real Genetic Mutations That Sound Like Superpowers
- Friday April 3, 2026
- Science | Edited by Nikhil Pandey
Scientists have identified rare genetic mutations granting extraordinary abilities, including minimal sleep, extreme strength, and reduced fear or pain responses.
-
www.ndtv.com
-
Doctors Express Concern Over Child Diagnosed With Chronic Disease Typically Seen In Adults
- Wednesday April 1, 2026
- Health | Press Trust of India
Doctors in a Delhi NCR hospital have reported a rare case of chronic pancreatitis in a 10-year-old girl, a condition typically associated with prolonged alcohol and tobacco use in adults, raising concern among specialists.
-
www.ndtv.com
-
Catherine O'Hara Lived With Situs Inversus. What The Genetic Organ-Placement Condition Means
- Saturday January 31, 2026
- Lifestyle | Written by Krati Purwar
"I am a freak," said Catherine O'Hara, laughing about the genetic condition in which her organs were flipped
-
www.ndtv.com/lifestyle
-
Stranger Things Star Gaten Matarazzo Was Born With Cleidocranial Dysplasia, Know About The Rare Genetic Condition
- Thursday January 1, 2026
- Lifestyle | Written by Krati Purwar
Stranger Things star Gaten Matarazzo was born without collarbones, and the rare genetic condition has affected his teeth and height
-
www.ndtv.com/lifestyle
-
The Invisible Disorder: An Indian Mother Shares How An Ultra-Rare Genetic Disease Reshaped Her Family's Life
- Thursday December 11, 2025
- Health | Written by Shreya Goswami
Norrie Disease is an ultra-rare genetic disorder causing congenital blindness, progressive hearing loss and neurological challenges. One Indian mother's journey reveals how misunderstood the condition is, and why early genetic screening and awareness
-
www.ndtv.com
-
Did Adolf Hitler Really Have A Micropenis? Rare Genetic Disorder Kallmann Syndrome Explained
- Saturday November 15, 2025
- Health | Written by Shreya Goswami
Kallmann Syndrome is a rare genetic disorder that causes delayed puberty and a poor sense of smell. New DNA findings suggest Adolf Hitler may have had features of this condition.
-
www.ndtv.com
-
Rare Orange Shark Spotted In Costa Rica, Experts Reveal Reason Behind Its Bright Colour
- Wednesday August 27, 2025
- Offbeat | Edited by Srishti Singh Sisodia
More research is needed to explore potential genetic or environmental factors influencing this rare pigmentation anomaly in sharks.
-
www.ndtv.com
-
Indian-Origin Man Claims London Cafe Refused Him Service Because Of His Face: "Everyone Was Staring At Me"
- Sunday May 18, 2025
- World News | Edited by Ritu Singh
He described the experience as distressing, saying that everyone in the cafe was staring at him, making him feel like a "ghost".
-
www.ndtv.com
-
"Everyone Is A Cousin" In This Village. Courtesy: A Rare Genetic Condition
- Monday May 12, 2025
- World News | Edited by NDTV News Desk
A small village in Brazil is afflicted with Spoan syndrome, a rare hereditary illness that weakens the body over time by affecting the nervous system.
-
www.ndtv.com
-
Model Katie Price "Heartbroken" Over Son Harvey's Health, Says He's At Risk Of Heart Attack
- Monday April 21, 2025
- Feature | Edited by Anjali Thakur
Harvey, who lives with a rare genetic condition called Prader-Willi syndrome, now weighs close to 30 stone (around 188 kg).
-
www.ndtv.com
-
Olivia Farnsworth: UK Girl Who Feels No Pain, Hunger, Or Fatigue
- Thursday March 13, 2025
- World News | Edited by Nikhil Pandey
Olivia Farnsworth, a UK girl, has a rare genetic condition that makes her insensitive to pain, hunger, and fatigue, posing significant health risks and requiring constant monitoring and management to ensure her well-being.
-
www.ndtv.com
-
17,000-Year-Old DNA of Ice Age Infant Reveals Dark Skin, Blue Eyes
- Monday October 28, 2024
- Written by Gadgets 360 Staff
Analysis of a 17,000-year-old infant’s remains from southern Italy sheds light on Ice Age ancestry and health. The infant, found in a Puglian cave, was likely around a year old at death and had distinctive traits—brown skin, blue eyes, and curly dark hair. His genome links him to Europe’s Villabruna lineage, suggesting their presence in south...
-
www.gadgets360.com