New Study Identifies Gene Related To hEDS
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Mon Jul 29 17:37:27 BST 2024
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New Ehlers-Danlos Syndrome Research Update
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New Study Identifies Connection Between Hypermobile EDS And The KLK15 Gene
Recent advancements in genetic science, highlighted by a study from https://links.dna.sequencing.com/web-only/z/k70zuy710mnk04?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=882c2a3b-a591-42e2-99b1-f1dd3ed061e9&mid=2093d71f-e2f9-4588-b5c0-893203ed3ba4&bsft_ek=2024-07-29T16%3A00%3A08Z&bsft_mime_type=text&bsft_tv=32&bsft_lx=3[Norris Lab](https://links.dna.sequencing.com/web-only/z/k70zuy710mnk04?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=882c2a3b-a591-42e2-99b1-f1dd3ed061e9&mid=2093d71f-e2f9-4588-b5c0-893203ed3ba4&bsft_ek=2024-07-29T16%3A00%3A08Z&bsft_mime_type=text&bsft_tv=32&bsft_lx=4), have significantly expanded our understanding of hypermobile Ehlers-Danlos Syndrome (hEDS). This research has uncovered a variant in the KLK15 gene associated with hEDS, offering new insights into potential causes.
Hypermobile EDS is a connective tissue disorder characterized by symptoms such as joint hypermobility, skin hyperextensibility, and tissue fragility. Our genetic test can help identify markers for all types of EDS including the variant of the KLK15 gene associated with hEDS.
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How To Screen For Ehlers-Danlos Syndrome
Including The KLK15 Gene Variant
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Get Whole Genome Sequencing
Our Whole Genome Sequencing service screens for all types of EDS, including hEDS, providing a thorough analysis of the genetic variations associated with this group of disorders.
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