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Girl with
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Syndrome Treatment
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1:32
ANTLEY BIXLER SYNDROME : What is Antley Bixler syndrome ? - Antley bixler syndrome symptoms
2.3K views
May 21, 2020
YouTube
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Understanding Antley Bixler Syndrome: Josephine's Story
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Feb 27, 2021
TikTok
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Josephine's Journey with Antley Bixler Syndrome
56.1K views
4 months ago
TikTok
annaowenn
0:41
It’s craniosynostosis awareness month!! Josephine was born with syndromatic bicoronal craniosynostosis caused by Antley Bixler Syndrome She’s had three brain surgeries to reconstruct her skull to make room for her brain and her eyes. She has probably one more before we will be done with head surgeries. We have had AMAZING providers at our children’s hospital and without them, Josie wouldn’t be here with us. Hug a cranio kid today! | Anna Owen
6.7K views
9 months ago
Facebook
Anna Owen
0:07
Josephine's Journey: Overcoming Antley Bixler Syndrome
Jul 15, 2022
TikTok
annaowenn
0:25
Anna Grace Owen on Instagram: "Happy world rare disease day! Josie has Antley Bixler Syndrome which is 1 in 250 million. She also fails into the 1 in 4 of her Syndrome which makes her even more special! Some traits of ABS: Craniosynostosis Radial-humeral synosyosis (her 90⁰ arms) Deformed feet Midface hypoplasia Narrow ear canals Josie also loves dinosaurs, dancing, making jokes, stacking blocks, her siblings, her cat and dog, going to church, going to therapy, trying new foods, and loves her mo
57.9K views
Feb 28, 2023
Instagram
annaowen
0:10
Josephine's Rare Battle with Antley Bixler Syndrome
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Jul 1, 2022
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0:05
Anna Grace Owen on Instagram: "Hi! This is Josephine Grace. She was born May 29, 2020. Some fast facts about Josie: She has a super rare condition called Antley Bixler Syndrome. It only affects about 1 in 250 million people. So she's pretty special. She also has bicoronal craniosynostosis and has had two brain surgeries to help correct it. At 3 weeks old, Josie got a tracheostomy tube so she could breath. She has microfacial hypoplasia and couldn't breath through her nasal passages, so she neede
65.4K views
Oct 24, 2022
Instagram
annaowen
0:40
Anna Grace Owen on Instagram: "It’s craniosynostosis awareness month!! Josephine was born with syndromatic bicoronal craniosynostosis caused by Antley Bixler Syndrome She’s had three brain surgeries to reconstruct her skull to make room for her brain and her eyes. She has probably one more before we will be done with head surgeries. We have had AMAZING providers at our children’s hospital and without them, Josie wouldn’t be here with us. Hug a cranio kid today!"
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Kim Peek: The Real-Life Human Google with Absolute Memory
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Werner Syndrome is a rare condition that causes premature aging, often starting in the teenage years or early adulthood. People may experience: • Early gray hair • Wrinkled skin • Cataracts • Diabetes • Weak bones • Heart disease It is caused by mutations in the WRN gene and is inherited from both parents. There is no cure yet, but treatment helps manage symptoms and improve quality of life. Aging is natural. Premature aging disorders are medical conditions. 💜
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tagiekyananulinuli
4:36
Assalamualaikum salam jumaat semua ❤️ Ramai yang tanya Hafiy sakit apa ? Di sini saya ringkaskan sebagai seorang ibu kepada anak syurga . Hafiy disahkan menghidap Antley Bixler Syndrome keadaan di mana tulang tengkoraknya bercantum terlalu awal sejak dalam kandungan. Saya hanya tahu tentang keadaan Hafiy sebaik dia lahir, di Labour Room saat pertama kali saya menyambutnya, Allah titipkan bersama satu ujian yang penuh hikmah. Hafiy bukan anak biasa. Dia anak syurga yang Allah pilih dengan perjal
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