How is Juliana Wetmore doing?
But Juliana is now thriving, attending elementary school in Clay County, Florida. She can talk and also uses sign language to communicate. Her parents are hopeful that her tracheotomy tube will one day be removed and that she will also learn how to eat on her own.
Is it possible to be born without a face?
Baby born without face due to rare condition defies odds to celebrate first birthday. A baby boy who was born without a face has defied all the odds to reach his first birthday. The rare congenital disorder means the flat bones in the cranial vault within the skull are either completely or partially absent.
What happened to the girl with no face?
— Juliana Wetmore is known around the world as “The Girl Born Without a Face.” Her story went viral a year after she was born. Her face didn’t look human when she was born. Juliana has a genetic condition called Treacher Collins syndrome. She’s missing up to 40 percent of the bones in her face.
What causes Treacher Collins syndrome?
Mutations in the TCOF1, POLR1C, or POLR1D gene can cause Treacher Collins syndrome. TCOF1 gene mutations are the most common cause of the disorder, accounting for 81 to 93 percent of all cases. POLR1C and POLR1D gene mutations cause an additional 2 percent of cases.
Who is the kid with no face?
In 2012, Dr Andrew Rochford met an incredible young boy who had been hidden away by his family. Three-year-old Yahya was born in Morocco with a number of birth deformities that effectively left him without a face – he was blind, had no nose and his mouth was barely functional.
Is the man without a face still alive?
Markus Wolf/Living or Deceased
Who is the woman with no face?
Tambu Makinzi is a 27 year old mum of one from Zimbabwe and lives in Cape Town South Africa. She has been diagnosed with a rare form of bone cancer called chondrosacoma.
Why did tambu pass away?
But when Tambu Makinzi’s forehead began to swell, her fears were compounded. Doctors in South Africa told the 27-year-old she was suffering a rare bone cancer, chondrosarcoma. It devoured her whole face, eating away at her nasal and jaw bones, displacing her left eye and robbing her of her sense of smell.
What is life expectancy for someone with Treacher Collins syndrome?
Usually, people with Treacher Collins syndrome grow to become functioning adults with normal intelligence. With proper management, life expectancy is approximately the same as in the general population. In some cases, the prognosis depends on the specific symptoms and severity in the affected person.
What happened to Yahya the boy without a face?
Three-year-old Yahya was born in Morocco with a number of birth deformities that effectively left him without a face – he was blind, had no nose and his mouth was barely functional. His desperate parents tried everywhere for help, but were told there was nothing that could be done.
What happened to the boy without a face?
After intense reconstruction surgery, a three-year-old Moroccan boy born without a nose, eyes or a functioning mouth has been given a new lease on life. Yayha El Jabaly’s stunted bone formation in the womb left him unable to speak, without eyes, with a hole in for his nose and an upside-down upper jaw.
Is Juliana Wetmore still alive?
Juliana wetmore 2017 Girl is born with no face, 6 years later – 2017. Juliana is now 12-years-old, and has had 45 operations. But she now also has Danica who by experience is able to understand her challenges. This family’s courage is amazing and is truly an inspiration. Share this wonderful story of love and hope with those you love.
Why was Juliana Wetmore born without a face?
Juliana Wetmore is known as “the girl without a face.” One of the worse documented case of a genetic disorder called Treacher Collins Syndrome and it causes, Juliana was born with severe deformations of face due to missing bones. Four months before birth,…
Where does Juliana Wetmore go to elementary school?
But Juliana is now thriving, attending elementary school in Clay County, Florida. She can talk and also uses sign language to communicate. Her parents are hopeful that her tracheotomy tube will one day be removed and that she will also learn how to eat on her own. Juliana can talk and also uses sign language to communicate. (FCN)