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LAKEVILLE, Minnesota, June 13, 2017 (LifeSiteNews) — Ruby Ardolf is a 12-year-old with a rare genetic condition called Stromme syndrome that causes vision impairment, microcephaly, intestinal 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. At birth, these findings led doctors to believe that Ruby was completely blind in both eyes. Ruby has a rare genetic condition called Stromme Syndrome.

To me, Ruby was just Ruby and a label or diagnosis didn't change the way I treated her. Then in 2017, we were thrust into the public spotlight when Ruby's video went viral. Overnight, Ruby became a spokesperson for Stromme Syndrome. At that point, I felt it was important to have genetic testing done to confirm the clinical diagnosis. In May 2017, Ruby Ardolf (born November 11, 2004), from Minnesota, United States and diagnosed with Strømme syndrome, appeared in an Instagram video answering questions from her mother Angela which went viral, gaining over 500,000 views in a week.

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The intestinal atresia is of the "apple-peel" type, in which the remaining intestine is twisted around its main artery. LAKEVILLE, Minnesota, June 13, 2017 (LifeSiteNews) — Ruby Ardolf is a 12-year-old with a rare genetic condition called Stromme syndrome that causes vision impairment, microcephaly, intestinal She also has bilateral Peter’s Anomaly, which causes thinning and clouding of the corneas and makes Ruby’s eyes appear as if they do not have an iris (the colored part of the eye). Both of these conditions are part of Stromme Syndrome.

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Ruby is truly 1 in a million! 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.

What is Ruby’s diagnosis? Ruby has a rare genetic condition called Stromme Syndrome. She was diagnosed with this condition when she was in the NICU, but at the time, it was called “Apple-peel intestinal atresia, ocular anomalies and microcephaly syndrome,” which is basically just a listing of the “symptoms” of the syndrome. Ruby is 14 and has a rare genetic condition called Stromme Syndrome. Angie is her momma and cheerleader.
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Affected individuals typically have some type of intestinal atresia, variable ocular abnormalities, microcephaly, and sometimes involvement of other systems, including renal and cardiac. 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’s beginnings were pretty rough, who happened to be an unplanned pregnancy. Her father did not second his spouse Angie’s decision not to terminate the pregnancy medically.
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Trivia.

Angie and Ruby på Twitter: "Seeing the positive comments on SBSK

What is Stromme Syndrome? – Angie and Ruby Patients with Stromme syndrome will display a number of physical characteristics that will help medical professionals identify the condition.

Se hela listan på allhealthsite.com 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. 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.