What Is Coffin-Lowry Syndrome (CLS)? Signs, Causes, Diagnosis And Treatment Of This Rare Genetic Disorder
What Is Coffin-Lowry Syndrome (CLS)? Signs, Causes, Diagnosis …
Feb 11, 2021
onlymyhealth.com
Dave is diagnosed with Coffin-Lowry syndrome. This rare genetic condition makes it difficult for him to walk, talk and live independently. If he had one wish, Dave would want to "smile and stay happy". | Special Books by Special Kids
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Living with Li-Fraumeni Syndrome: Patients Share Their Experiences
Living with Li-Fraumeni Syndrome: Patients Share Their Experiences
Mar 19, 2021
utah.edu
Coffin-Siris syndrome is a rare genetic condition that is caused by variants in one of several genes. Depending on the mutated gene, several body systems can be affected that then causes a variety of symptoms. There are only 500 cases of Coffin-Siris syndrome known worldwide. This month, we’ll be sharing the stories of 3 kids who are part of the Coffin-Siris syndrome community: Ruby, Stella, and Auron. Even among these three little warriors, CSS shows up differently. 💜 For Ruby, the main proble
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