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Crigler-Najjar syndrome Type-I is inherited as an:... | Filo
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Crigler najjar Syndrome
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Kelly est atteinte du syndrome de Crigler-Najjar, une maladie génétique rare du foie. Pour éviter de graves dommages neurologiques, elle doit utiliser la photothérapie et passer 10h par jour sous 390 LED. Généthon, le laboratoire du Telethon, a mis au point un traitement de thérapie génique qui montre des premiers résultats encourageants. Sa vie d'ado de 15 ans, voici comment elle la vit. #Téléthon2023 | Brut
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De nouveaux résultats préliminaires de l’essai mené par Généthon concernant le syndrome de Crigler-Najjar, une maladie rare du foie, ont été présentés au congrès de l’ESGCT le 22 oct. Résultats encourageants commentés par Dr D’Antiga qui a traité les patients de la 2e cohorte 👉 https://bit.ly/2ZgjXLh | Téléthon
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372K views · 13K reactions | Kierra is diagnosed with a rare genetic condition known as Nager syndrome. She hopes that others understand that each person in the world is a human worthy of acceptance. | Special Books by Special Kids | Facebook
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