Her genetic tests came back inconclusive, but she was clinically diagnosed with a condition now known as Stromme Syndrome. It was so rare at the time that only

Both of these conditions are part of Stromme Syndrome. At birth, these findings led doctors to believe that Ruby was completely blind in both eyes. However, as time went on, we realized that she has light perception in both of her eyes.

One of the most notable case of Stromme syndrome is involving Ruby Ardolf which born in 2004. In May 2017, Ruby who’s diagnosed with Stromme Syndrome appeared in an Instagram video answering questions from her mother Angela which went viral, gaining over 500,000 views in a week. The incidence rate or prevalence of Stromme syndrome is not yet Stromme syndrome is an autosomal recessive congenital disorder affecting multiple systems with features of a ciliopathy. Affected individuals typically have some type of intestinal atresia, variable ocular abnormalities, microcephaly, and sometimes involvement of other systems, including renal and cardiac.

Ruby is 1 of 12 known cases of Stromme syndrome in the world. Join her as she goes about a typical day at school. SBSK Patreon: https://www.patreon.com/SBSKS Meet Ruby! #littlestwarriorwednesday Ruby is a 13-year old with a rare genetic condition called Stromme Syndrome, which causes vision impairment, microcephaly, intestinal issues, slowed growth and developmental delays. As far as Ruby's mom, Angie, knows, there are fewer than 50 cases of Stromme Syndrome in the world! When Ruby was a baby, doctors told Angie that Ruby would not talk, walk or do People with Stromme syndrome typically have intestinal atresia (missing part of the intestine) eye abnormalities and microcephaly (smaller head).

There is as yet no cure available for Stromme syndrome, but the patient can often be treated to at least help ensure their survival and/or enhance their quality of life. Many patients will need to undergo surgery on their digestive system, and/or on their heart. Our heart has 4 chambers: 2 ventricles and 2 atria.

Ruby is 1 of 12 people in the world diagnosed with Stromme syndrome.She hopes that those who get to meet her take a moment to say "hi."SBSK Patreon: https://

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One of the most notable case of Stromme syndrome is involving Ruby Ardolf which born in 2004. In May 2017, Ruby who’s diagnosed with Stromme Syndrome appeared in an Instagram video answering questions from her mother Angela which went viral, gaining over 500,000 views in a week. The incidence rate or prevalence of Stromme syndrome is not yet

She shares both an Instagram and YouTube channel with her mother called Angie and Ruby. Before Fame. She developed a rare genetic condition called Stromme Syndrome. Trivia. Her mother used the support they found on Instagram to raise $15,000 on GoFundMe in under a week for a future support dog. Family Life Ruby is a 12-year old with an extremely rare genetic condition called Stromme Syndrome, which causes microcephaly, vision impairment, bowel obstruction, short stature and developmental delays. There are only 12 known cases of this condition in the world!

Syndrome de Stromme. Par Dorothy Cummings McLean (LifeSiteNews) traduit par Campagne Québec-Vie Ruby Ardolf est une jeune fille de 12 ans, atteinte d'une maladie génétique rare, le syndrome de Stromme, qui cause une déficience visuelle, la microencéphalie, des problèmes intestinaux, un retard de croissance et des troubles de développement This information comes directly from the OMIM 9 Oct 2019 Ruby Ardolf, 14, has her own YouTube channel, featuring familiar of 12 people worldwide with a genetic condition called Stromme syndrome, 3 Oct 2018 Ruby is a 13-year old with a rare genetic condition called Stromme Syndrome, which causes vision impairment, microcephaly, intestinal issues, Her genetic tests came back inconclusive, but she was clinically diagnosed with a condition now known as Stromme Syndrome. It was so rare at the time that only In this video, CEO Chris Ulmer interviews 12-year-old Ruby Ardolf, one of fewer than 50 people in the world with a genetic condition called Stromme Syndrome. 6 Apr 2018 One of the sweetest interviews I have ever seen. Ruby is one of 12 people in the world who has Stromme Syndrome, and also one of the happiest Ruby is a 14-year-old sweet and sassy teen girl with a rare genetic condition called Stromme Syndrome, which causes a vision impairment, microcephaly and 7 Jun 2017 Stromme syndrome. 11 years after she was born, Angie finally found the name of the syndrome Ruby has. Stomme syndrome is a very (4) Meet Angie & Ruby | Learn more about Stromme Syndrome - YouTube Disability ourselves and share a little more information on Ruby's genetic conditio.
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Stromme syndrome is an autosomal recessive genetic condition. Stromme Syndrome is an autosomal recessive congenital disorder which affects multiple organ systems in the body resulting in various clinical symptoms and signs.

How a person develops from this 19 Feb 2020 Stromme syndrome, or Apple peel syndrome, is a birth defect that can As of 2019, there is a case of a girl named Ruby with the syndrome 21 Oct 2019 Yet Ruby is not a typical teen vlogger. She is one of 12 people worldwide with an inherited condition called Stromme syndrome, which results related video Inclusion: Ruby's Story: This video is about a girl named Ruby, who has Stromme Syndrome. Ruby's mom shares her initial hesitation about 9 Apr 2021 Check Angie and Ruby YouTube statistics and Real-Time subscriber Ruby is 14 and has a rare genetic condition called Stromme Syndrome. 15 Oct 2019 Meet Ruby.
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Ruby is 1 of 12 people in the world diagnosed with Stromme syndrome.She hopes that those who get to meet her take a moment to say "hi."SBSK Patreon: https://

In May 2017, Ruby who’s diagnosed with Stromme Syndrome appeared in an Instagram video answering questions from her mother Angela which went viral, gaining over 500,000 views in a week. The incidence rate or prevalence of Stromme syndrome is not yet Stromme syndrome is an autosomal recessive congenital disorder affecting multiple systems with features of a ciliopathy. Affected individuals typically have some type of intestinal atresia, variable ocular abnormalities, microcephaly, and sometimes involvement of other systems, including renal and cardiac.

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Ruby is 1 of 12 people in the world diagnosed with Stromme syndrome.She hopes that those who get to meet her take a moment to say "hi."SBSK Patreon: https://

Ruby is 14 and has a rare genetic condition called Stromme Syndrome.