Does a child's diagnosis unlock a family mystery? Patient advocate Sean P. Kelley shares how his daughter’s facial features led to a surprise Alagille Syndrome diagnosis for his wife. Learn the critical importance of family-based genetic screening. Watch the full video ➡️ https://www.facebook.com/events/1161801072573210 #CME | Medscape
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ASPIRE Internship: Research and Scientific Program Development, Alagille Syndrome Alliance (ALGSA), remote part-time
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Anna and Shambhavi, two rare disease patients from the Alagille Syndrome Alliance, traveled across the globe to meet the man – Kamesh Surendran, PhD – searching for answers to their disease. #UniteToCure https://san.fo/2qGZElc | Sanford Health
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Qu'est-ce que le Syndrome d'Alagille ?
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Alagille Syndrome shows typical facial features including broad forehead, deep-set eyes and pointed chin and abnormalities of liver etc. To know more about #alagillesyndrome or to seek an appointment with our specialists, visit: http://relainstitute.com/hospitals-chennai/institute-liver-diseases-and-transplant/alagille-syndrome Or simply call us on 91 9384681770 #featuresalagillesyndrome #alagillesyndrometreatmentspecialistinchennai #paediatriclivertransplantsurgeoninIndia #besthospitalforpaedia
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