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Rare Disease News

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Rare medical phenomenon: Baby found inside newborn’s abdomen; Doctors fight to save her

In Madhya Pradesh, a rare medical case was discovered where a baby was found inside the abdomen of a newborn. This condition, known as Fetus in Fetu (FIF), was identified during an ultrasound in a pregnant woman from Sagar district. ...
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What is Myostatin-hypertrophy? Condition causing muscles to grow excessively large

Myostatin-related muscle hypertrophy is a genetic disorder that impacts muscle growth regulation. Myostatin is a protein that normally inhibits muscle growth. When this protein is deficient or malfunctioning due to genetic mutations, muscles grow uncontrollably....
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What is fatal familial insomnia? Footage reveals harrowing reality of sleep disturbances leading to death

Fatal Familial Insomnia (FFI) is a genetic degenerative brain disorder marked by profound sleep disturbances. The condition begins with subtle difficulties in sleeping, which worsen progressively. As the disorder advances, individuals experience total insomnia, referred to as agr...
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Karnataka CM Siddaramaiah urges PM Modi for lifesaving aid for toddler's rare disease battle

Karnataka CM appeals PM Modi: CM Siddaramaiah has reached out to PM Modi to fund the medical treatment of young Maurya, who is battling a severe and rare health condition known as Spinal Muscular Atrophy (SMA)....
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Noida Urges Timely Check-Ups On Rare Disease Day To Protect Infants From Rare Diseases

Child PGI, a renowned medical institute in India, is treating a three-year-old child suffering from a rare disease that has never been detected in the country before. The child cannot speak, has frequent seizures, and is far behind in developmental milestones compared to other...

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