What Is Fabry Disease? Here Are The Symptoms, Causes, Treatment
What Is Fabry Disease? Here Are The Symptoms, Causes, Treatment
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🧬 Understanding Fabry Gene Inheritance Fabry disease is caused by a change (mutation) in the GLA gene on the X chromosome — which means it follows an X-linked inheritance pattern. Because Fabry can affect both men and women, family screening and genetic testing are key to early diagnosis and management. Knowing your genetic status can help you and your family get the care and support you need. 💙 #FabryAwareness #FabryDisease #Genetics #FSIG #FabryFamily #RareDisease | Fabry Support & Informati
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Fabry disease is a genetic disorder that is caused by a mutated gene on the X-chromosome. This means that it can be passed down from parents to their children if the parents carry the gene. If one member of a family is found to have Fabry disease, it is recommended that all members of that family are tested. See how Fabry disease is passed on genetically below and learn more here: https://bit.ly/4bfEJKx #FabryDisease #Genetics #Pharmaceutical #Healthcare | Idorsia Pharmaceuticals Ltd
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