No menu items!

Your baby was born with a “permanent smile”. There are only 90 cases in the world, and parents don’t know what to do.

Share This Post

- Advertisement -

Your baby was born with a

- Advertisement -

Ayla Summer Mucha was born in December 2021 with bilateral macrostomia, where the corners of the mouth do not fuse during pregnancy.

- Advertisement -

Baby born in Australia In a rare condition that you seem to have “Permanent smile” Even if it ’s for his parents Constant learning every day.

Ayla Summerhays Born in December 2021 Isolated bilateral macrostomia, A malformation in which the corners of the mouth do not fuse during pregnancy. Based on the latest data 10 years ago, only about 90 cases have been reported worldwide in this condition.

parents, Cristina Vercher (21 years old) and her husband Blaize Mucha (20 years old) They are currently consulting with a doctor about surgery to correct his wide smile. Today, near the age of six months, babies can no longer eat breast milk because they can’t get caught in their mother’s nipples.

Ayla Summer Mucha was born in December 2021 with bilateral macrostomy. This is a rare disease with less than 100 registered cases worldwide.

Ayla Summer Mucha was born in December 2021 with bilateral macrostomy. This is a rare disease with less than 100 registered cases worldwide.

Parents to seek more information and raise awareness Opened a TikTok account To share your experience.

Christina said: “The only thing I could think of as a mother was where I was wrong, especially when I was pregnant all the time, but some doctors have assured us of this condition. It was completely out of our control And it wasn’t our fault. ”

“We haven’t received the exact specifications of the surgery yet, but we know it. With skin closure leaving minimal scarring.. The challenges faced after surgery are worrisome for couples. “

For medical reasons, patients with aria conditions are advised to undergo surgery to help make sure they have Mouth that works as they get older.

Blaize Mucha, parents of Cristina Vercher and her husband Ayla, are currently consulting with a doctor about baby surgery.

Blaize Mucha, parents of Cristina Vercher and her husband Ayla, are currently consulting with a doctor about baby surgery.

Doctor Flinders Medical Center in Adelaide, ..In Australia, they were initially confused because they had never seen a case before and were not detected by prenatal scanning.

The clip of the mother dressing her daughter Browse 46 million pages Social networks, and users flooded the comments section with support. “Social media is a fragmented place. Unfortunately, you can’t control the personality of others, but Blaze and I receive as much love and support as negative feedback,” said Christina. I am. “

Ayla Summer Mucha is followed by millions of people through the TikTok account that parents created to talk about her life experience.

Ayla Summer Mucha is followed by millions of people through the TikTok account that parents created to talk about her life experience.

Macrostomia Cleft lip and palate Between the maxilla and mandible, it derives from the first change in the gill arch and is unilateral or bilateral. It’s a congenital malformation, and as Christina said, parents can’t do anything to avoid it. There are many registered cases, but few at a level that Ayla rarely has.

“On social media, Blaze and I have received as much love and support as negative comments. Thank you for posting the video Because I talked to some mothers who had similar experiences. That’s why we never stop showing our experience, “she said.

Source: Clarin

- Advertisement -

Related Posts