Top 21 kids has extra ordinary feature you won’t believe exist.
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Top 21 kids has extra ordinary feature you won’t believe exist. Before we begin, click that like button to inspire us. Moreover, subscribe to our channel and click the notification bell to be influenced by this type of ultimate fact. […]
Top 21 kids has extra ordinary feature you won’t believe exist. Before we begin, click that like button to inspire us. Moreover, subscribe to our channel and click the notification bell to be influenced by this type of ultimate fact.
All kids are unique in their own way, but some are more unique than others. From the super strong to the incredibly beautiful. These kids need to be seen to be believed. Here are ten kids you won’t believe exist.
Parasitic twin
A baby was born in a hospital in Jaipur, and her family could not believe what they were seeing. She was born with a head attached to her stomach. It was a parasitic twin that was feeding off of her blood supply, depriving the baby of the nutrients that she needed. The twin had a head with no ears or eyes; it also had a hand. Luckily, the doctors were able to safely remove the twin.
Ollie Trezise
Ollie Trezise is an adorable boy, except for the fact that his brain is growing through a crack in his skull right into his nose. He suffers from a very rare condition called ensapalasay. He’s often referred to as a real-life Pinocchio. His condition made it very hard for him to breathe, so he has gone through several painful surgeries.
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Tessa Evans
Tessa Evans was born with a rare condition called arhenia, which means that she was born without a nose. She was also born with no sinuses and no sense of smell. She is the first person ever to have a cosmetic nasal implant fitted as she grows. It will encourage a new nose to grow from her stretched skin. When she’s a teenager, she’ll have a final nasal prosthetic fitted.
Kristina Pimenova
Kristina Pimenova is originally from Moscow, Russia. She has been called the world’s most beautiful girl. She’s only 10 years old and has been modeling since she was 3. She has been doing runway modeling since she was 4 years old and has millions of followers on her show. But there has been some controversy over comments made on some of the youth’s photos.
Pan Xianhang
In eastern China, Pan has been referred to as a fish boy due to a severe case of ichthyosis. This is a very rare skin condition that is presently incurable and causes dry, thick, and scaly-looking skin. He also has difficulty sleeping due to the itching and pain. Hopefully, one day, a cure can be found or at least a way to lessen the discomfort caused by the condition.
Ben Underwood
When he was only 2 years old, Ben Underwood of Elk Grove, California, was diagnosed with retinal cancer. In order to avoid the spread of the disease, his eyes were removed and replaced with prosthetics, unlike most visually impaired people. He was able to play basketball, rollerblade, and even ride a bike. Sadly, his cancer returned, and he passed away at the age of 16 in 2009.
Marcia and Millie Briggs
Marcia and Millie Briggs, from Birmingham, England, looked the same when they were born. However, as they got older, their skin tone became very different. Brown-eyed Millie started to get darker skin like her father Michael, and blue-eyed Marcia took on a lighter complexion with lighter hair like her mother Amanda. Even nobody believes that they’re twins.
Mohammad Kaleem
Mohammad Kaleem is a boy from India who suffers from a rare disease called localized gigantism. The condition causes his hands and arms to grow to a disproportionate size. He lived a very secluded life because the villagers would curse him and call him a devil’s child.
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Vincent Oketch
Vincent is a 10-year-old boy from Uganda whose legs started swelling up, which is called elephantism. It was soon discovered that he contracted a deadly flesh-eating infection as his condition worsened. He could no longer walk or wear his own clothes.
Luz Milagros Veron
A couple gave birth to a baby girl in Argentina in 2012 who was three months premature. The doctors declared her dead. About 12 hours later, they asked to go down to the morgue to say one last goodbye to their daughter. When they got there, the baby was moving around, and she started crying. Her parents were overjoyed, and they named her Luz Milagros Veron. Sadly, though, on her first birthday, she passed away.
Adalia Rose
Another young child is living with progeria. Adalia is a constant target of trolls and bullies, but she has learned to ignore them. Despite her condition, she is a social media phenomenon and an inspiration to other young girls. Her viral YouTube videos have earned her almost 15 million subscribers.
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Avery Ford was not an average baby when she was born. The average-sized baby is about 7 pounds, 5 ounces. However, Avery was 14 pounds, 1 ounce. When she was born, her mother didn’t even know she was pregnant until her third trimester, which makes it crazy that she gave birth to such a large baby. Her mother was in labor for 18 hours. However, she said it was all worth it to see her daughter’s beautiful face.
Lara and Mara Bawar
Laura and Maura, who are from Sao Paulo, Brazil, are very beautiful, and they’re very unique-looking. After photos of them went viral, a fashion photographer took their photo. Soon, they were signed by a top modeling agency. They even have a Swiss photographer who’s working on a project based solely on the twins called Flores Rarest, which means rare flowers.
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Bayezid Hossain
Byazid Hossein in southern Bangladesh suffers from progeria, a condition that causes premature aging of the body but not the mind. While Byazids do have above-average intelligence, His sagging skin, deep-set eyes, and other abnormalities caused by the condition give him the appearance of an 80-year-old man. His parents have sought out different doctors, shamans, and healers to help their son, but he may not be 15 years old.
Hyomung Shin
Shin suffers from Highlander syndrome, a condition that slows the aging process. Shin is actually 26 years old. Due to his youthful face and high-pitched voice, he is often mistaken for an elementary school student. He has been dubbed the Peter Pan of Korea. But doctors say the condition does not affect his overall health.
Asher Nash
After being turned down by a modeling agency in Buford, Georgia, this little guy’s mother set out on a quest to speak out about the incident. Asher was born with Down’s syndrome, and this may have been a factor in his rejection. His story went viral, and he has since modeled with OshKosh B’gosh and Toys ‘R’ Us.
Shiloh Pepin
Shiloh Pepin was born with sirenomelia, or mermaid syndrome, which caused her to be born with her legs fused together from the waist down. Infants born with this condition can sometimes have their legs surgically separated, but due to the blood vessels crossing from side to side, she could not have her legs separated. However, Shiloh passed away in 2009 at 10 years old due to complications from pneumonia.
Richard Sandrak
Richard Sandrak is known as Little Hercules. In his youth, Richard Sandrak was named the world’s strongest boy by the time he was 11 years old. His father was a martial arts world champion and began training his young son. At the age of 6, he could bench press a hundred and eighty pounds. His training included 600 push-ups as well as 300 squats a day. He is now a stuntman at Universal Studios Hollywood.
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Johncris Carl Quirante
At just 9 years old, Johncris Carl Quirante from the Philippines is a local curiosity.
started when his parents realized he was growing more than the typical baby teeth. It wasn’t until he was 5 years old that he received his first x-rays. The dentist was shocked to see over a hundred and fifty teeth on the boy’s images. His condition worsened until he had more than 300 teeth crowding his mouth.
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Charlotte Garside
Although she’s nine years old, this little girl is still mistaken for a baby. She may even be one of the smallest girls in the world. She was born with primordial dwarfism, and at age 9, she weighed just over 9 pounds. But she’s no baby! She’s just a regular kid, but a bit smaller.
Jaxon Buell
Jaxon Buell was born in 2014 with the point of his brain and his head missing. His parents did not want to erminate, and they had their baby and named him Jaxon. They were very happy that they gave Jackson a chance because he lived longer than doctors ever predicted. He had been called a miracle child, and he even has a huge following on social media.
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