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7 kiểu người dễ mắc ung thư gan nhất, xem lại mình ngay

7 kiểu người dễ mắc ung thư gan nhất, xem lại mình ngay
kienthuc.net.vn - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from kienthuc.net.vn Daily Mail and Mail on Sunday newspapers.

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Vợ bị băng huyết sau sinh, chồng chăm hết mực đến khi khỏe lại liền đưa đơn ly hôn

Vợ bị băng huyết sau sinh, chồng chăm hết mực đến khi khỏe lại liền đưa đơn ly hôn
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You can help this 10-year-old walk


You can help this 10-year-old walk
Mumbai Mirror / Updated: May 9, 2021, 06:00 IST
.
Mohin Mamania (in pic), a 10-year-old from Mulund, cannot run around his school or play with his friends, like other children do. The reason:
Mohin suffers from the
genetic disorder characterised by progressive muscle degeneration and weakness.
The condition is usually diagnosed around the age of four, and by the time the child reaches the age of 11-12 years, they lose locomotive abilities in their hands too, and have to depend on a wheel chair. They can also have a short life span.
A drug called Viltepso that was launched in the United States last year offers hope, but the ....

Himachal Pradesh , United States , Mohin Mamania , Chirag Mamania , Muscular Dystrophy , Mohin Suffers , Genetic Disorder , Duchenne Muscular Dystrophy , Ld Md , இமாச்சல் பிரதேஷ் , ஒன்றுபட்டது மாநிலங்களில் , தசை டிஸ்ட்ரோபி , ஜெநெடிக் கோளாறு , ட ம்ட் ,

Brazil: Family of 14 all born with 12 fingers and toes


Brazil: Family of 14 all born with 12 fingers and toes
Brazil: Family of 14 all born with 12 fingers and toes
All The Members Of The Family Were Born With Six Fingers In Hands And Six On Their Feet, Including The Youngest Member, A Baby Boy Born With The Same Rare Genetic Abnormality.
News Nation Bureau | Edited By : Himani Garg
| Updated on: 14 Oct 2017, 04:29:06 AM
New Delhi:
The De Silva s, a family of fourteen members in Brazil have stunned everybody around with an unusual trait in the family. All the members of the family were born with six fingers in hands and six on their feet, including the youngest member, a baby boy born with the same rare genetic abnormality. ....

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Advanced computer model could lead to improvements in 'bionic eye' technology


Advanced computer model could lead to improvements in bionic eye technology
There are millions of people who face the loss of their eyesight from degenerative eye diseases. The genetic disorder retinitis pigmentosa alone affects 1 in 4,000 people worldwide.
Today, there is technology available to offer partial eyesight to people with that syndrome. The Argus II, the world s first retinal prosthesis, reproduces some functions of a part of the eye essential to vision, to allow users to perceive movement and shapes.
While the field of retinal prostheses is still in its infancy, for hundreds of users around the globe, the bionic eye enriches the way they interact with the world on a daily basis. For instance, seeing outlines of objects enables them to move around unfamiliar environments with increased safety. ....

Gianluca Lazzi , Fredh Cole , Emily Henderson , Viterbi School Of Engineering , Institute For Technology , Keck School Of Medicine , Provost Professor , Electrical Engineering , Keck School , Neural Systems , Rehabilitation Engineering , Scientific Reports , Genetic Disorder , Retinitis Pigmentosa , எமிலி ஹென்டர்சன் , விட்டர்பி பள்ளி ஆஃப் பொறியியல் , நிறுவனம் க்கு தொழில்நுட்பம் , கேக்க் பள்ளி ஆஃப் மருந்து , புரோஸ்ட் ப்ரொஃபெஸர் , மின் பொறியியல் , கேக்க் பள்ளி , நரம்பியல் அமைப்புகள் , புனர்வாழ்வு பொறியியல் , அறிவியல் அறிக்கைகள் , ஜெநெடிக் கோளாறு ,