10 Children With A 1 In 1,000,000 Chance Of Having A Baby

Miracle Babies: The Incredible Story of 10 Children Defying the Odds with a 1 in 1,000,000 Chance of Having a Baby

Children often hear about how special and unique they are. There are not so many people who are radically different from the rest. Here are 10 children about whom they say: "1 in 1,000,000." All of them suffer from hereditary diseases.

“Most strange diseases are due to a gene mutation. As it is right, this is a failure in the chromosomes. Until now, geneticists cannot say for sure what exactly provokes the birth of a child with abnormalities in absolutely healthy parents. Bad habits such as alcoholism and smoking can increase the risk of having a handicapped child. But not always. Sometimes a non-drinking and non-smoking woman gives birth to a baby with a gene mutation. Only one thing is known for sure: after 35 years, the probability of having an unhealthy child is 3-4%. At the same time, it is the age of the woman, not the man, that influences.

Doctor geneticist of the highest category, Zakharova Olga Mikhailovna

Statue Man Luciana Vulcan

A girl from the UK suffers from a rare disease that affects one in 2 million children. The muscles of her body turn into bones. Gradually, Luciana will become a statue. This disease is called fibrodysplasia ossificans progressive.

Fibrodysplasia ossificans progressive is a genetic disease caused by a mutation in a specific gene.

The diagnosis was made when the girl was 2 years old. Soon, Luciana could only use her left hand, because. the right hand was numb. She should not make sudden movements and falls lead to the growth of the disease. A small bruise causes excruciating pain.

Angus Palms - The Eternal Child

We often hear about children who age early. Angus' case is different - the boy stopped growing at 3 years old. Now he is 13 years old, but the appearance of a teenager is still like that of a three-year-old child. Doctors believe that it is a chromosomal disorder. Since this is the only such case in the world, Angus is 1 in 7,858,772,993 people.

Brave boy Angus Palms who stopped growing at the age of three

The boy's parents say that their child does not know how to talk, only groans and sniffles. Angus' mother realizes that her son will always depend on her. He will no longer become independent, which means that his parents should always be there.

Scales Instead Of Skin. Annabelle Whitehouse

At the age of 5, the girl gained fame thanks to the media. The girl was diagnosed with a rare skin disease Ichthyosis or "fish scales". She, like a snake, sheds her skin, but unlike a cold-blooded animal, this happens 14 times a day.

The disease is transmitted by heredity. Annabelle has congenital ichthyosis. She was born with a colloidal membrane that covered the entire body of the baby. The doctors removed the film, and the parents were able to examine their daughter. Thus began the fight against Annabelle's disease. Special moisturizers have become a part of the girl's life.

This is what the skin of a person suffering from ichthyosis looks like.

Isaac Hughes - A Boy Without Emotions

Isaac was born with paralysis of the facial muscles. This means that he cannot speak, and it is difficult for him to eat. The boy does not laugh, does not smile, cannot cry. This is how he lives since birth. His diagnosis is Mobius syndrome.

Isaac's Moebius Syndrome is a genetic hereditary disease.

Isaac has limited speech, and it is impossible to read the emotions on his face. But the child has great willpower, he is an active and cheerful boy. Unfortunately, some people think otherwise. Parents have to explain what kind of disease it is because their son is often criticized. But Isaac does not despair, he is a very sociable child. His situation is difficult - the disease is incurable.

Kylie Halko Is An Old Young Teen

American Kylie Halko was born with a disease of premature aging - progeria. The girl has grown old, not even reaching adolescence. She looks 8 times older than her age but leads an active life with her peers. The girl is popular on social networks, she has 200 thousand followers on Instagram. Kylie loves to sing.

Cheerful Kylie Halko wins hearts

Kylie is 15 years old, but her internal organs and biological clock are 85 years old. People with progeria rarely live to that age. It is not known how much she has left, but Kylie believes that this short life should be lived to the maximum.

Children Deprived Of Legs 

Fayez Ahmed Perrey grew and developed as expected. The accident made him an invalid overnight. At 4, Fayez and his sister were playing in the wasteland. They found an unexploded grenade. The boy hit the grenade with a bat, there was an explosion. His sister died instantly, and Fayez lost both legs.

Children's games sometimes end in an accident. Take care of the children!

The child spent three months in the hospital. He was given prostheses. The boy skillfully moves on artificial legs and plays cricket. He understands that he will not get into a team of professional players. This does not prevent him from being active and enjoying life.

Juliana Whitmore - Girl Without A Face

The diagnosis is Treacher-Collins Syndrome. This disease is characterized by craniofacial deformity. The syndrome, first described in 1900 by ophthalmologist E.T. Collins, occurs in one in 50,000 people. There are no mild forms of this disease. Severe deformation of the ears, nose, and bones of the face leads to deafness, problems with breathing and swallowing.

Doctors gave Juliana Whitmore hope for a normal life

Juliana is missing 40% of her facial bones. Until the age of 12, she was operated on 45 times. The main goal of the doctors was to enable her to do ordinary things. For example, eat, drink, talk. Juliana understands other people. She has learned to communicate with gestures and can hear.

Clever Boy Ramses Sanguino

Ramses spoke Russian at the age of 2, and Japanese at the age of 2. At the age of 4 he solved equations, at the age of 5 he mastered algebra. What is wrong with the child? He was diagnosed with autism. Ramses' mother reveals that her son is a telepath. He reads the thoughts of others from a distance and transmits his own. This alarmed those around him.

This pretty child was called autistic because he speaks several languages ​​and counts well

Scholars have become interested in the history of Ramses. They were doing research. The child really knows several languages and is good at mathematics. He calls the numbers guessed by the researchers exactly in the sequence in which they are secretly recorded. He has amazing intelligence.

Sophie Green: legs replaced hands

A girl of Chinese descent was born without arms. But she deftly copes with the help of her legs. This makes Sophie special. The adoptive parents are enthusiastic about Sophie. She draws, writes, and rides a bicycle. Engaged in vigorous activity, having only legs.

She eats while holding a spoon and fork with her toes. At the same time, the girl loves to sing and dance. Sophie does ballet and gymnastics. She is one of 10 adopted children in the family. All of them are handicapped. Parents devote all their free time to the development of their children, and Sophie helps them. She is an inspiration to the family. One of her radiant smiles is worth a lot.

Sophie is a little girl with a bright soul and a pure heart.

Ever Odet - Sleepless Beauty

Ever has Angelman syndrome. A girl from birth sleeps only 90 minutes at night. This is enough for her to sleep. In addition, Ever always smiles and rarely gets upset. She has a lot of energy despite her lack of sleep. Everything seems to be fine, but the girl will never be able to speak.

This disease is caused by a gene mutation. In young children, in addition to sleep disturbance, psycho-emotional and physical development is disturbed. In fact, smiling is a sign of deviation, not joy. This genetic disease is incurable. Ever does not know about this and continues to smile.

Children with Angelman syndrome always smile and seem cheerful, but no one knows what is going on in their souls.