Top Tweets for #AADCD
We are pioneering innovative treatments for patients around the world and are proud to share that our #genetherapy for AADC deficiency (#AADCd) has received approval in Hong Kong.
Stop by booths 529 and 531 to meet our team at the @AmEpilepsySoc Annual Meeting! Learn about #genetictesting for patients with suspected neurotransmitter disorders, as well as #AADCdeficiency as a potential underlying diagnosis in patients with suspected seizures. #AADCd
#AADCDeficiency is a rare disease that leaves children very dependent and fighting for life. Fortunately, Rylae-Ann had life-saving gene therapy for #AADCd. She has made amazing progress by working hard. Today, she has a message for AADC families. https://t.co/LyWUCRNOtt
If you are an HCP attending the Society of Inborn Errors of Metabolism (#SSIEM) 2023 Symposium, please join us tomorrow for our symposium discussing aromatic L-amino acid decarboxylase deficiency (#AADCdefieciency #AADCd). We invite you to also stop by booth A09 to meet our team!
Very interesting session by Dr Sheila Wong from HK Children’s Hospital at #AOCCN2023 sharing how important it is to not miss #neurometabolic and #inheritedmetabolic disorders, including #AADCd.
Here are a few reasons @_RafaelSierra is looking forward to moderating our sponsored symposium on #AADCdeficiency with Prof. Hwu, Dr. Chien and the Poulin family. Join us on August 5 in Bangkok, Thailand. #AOCCN2023 #AADCd
Gain insights on diagnosis and the impact of #AADCdeficiency from experts and caregivers at our symposium on August 5 at the 16th Asian Oceanian Congress of Child Neurology (AOCCN). #AADCd #AOCCN2023
“When you hear the term ‘rare disease,’ you think of very small numbers; however, there is a big network of rare disease families, and together we can make a much larger number,” says Richard Poulin. #AADCdeficiency #AADCd #raredisease https://t.co/NdPPqo03Ks
After her daughter was the fourth person diagnosed in the world with #AADCdeficiency, Kelly Heger became a pioneering advocate. We are continually inspired by her and the impact she has made on this community. #AADCd #raredisease https://t.co/4G15Bes5YS
Aromatic L-Amino Acid Decarboxylase Deficiency,
AADC deficiency, is a #genetic neurotransmitter disorder. The AADC enzyme helps make serotonin and dopamine. People with this #raredisease don’t make enough AADC enzyme 📑 https://t.co/fVVH6giMbG
Attending #SIMD2023? Meet the PTC Team at Booth 108 and learn about a rare neurometabolic disorder #aadcdeficiency. #neurometabolicdisorders #metabolicdisorders #aadcd #rarediseases
Are you attending #ACMG2023? Visit our team at Booth 508 to learn about #PTCPinpoint, a no-charge #genetictesting program to help support patients with suspected neurotransmitter disorders or Cerebral Palsy with unknown etiology. #aadcdeficiency #aadcd
Attending #ACMG2023? Stop by Booth 506 and meet Ryan Miller, a certified genetic counselor, to discuss the diagnostic challenges of #AADCd (Aromatic L-amino decarboxylase deficiency). #aadcdeficiency #raredisease #genechat
Thank you to @AADCFamilyNtwk for sharing your inspiring #AADCdeficiency story with @PharmaTimes. #AADCd #raredisease https://t.co/R5TtzgGh1X
#AADCdeficiency is a rare genetic disorder which is frequently misdiagnosed. Thank you @edu4rare for sharing your journey. #AADCd #raredisease
Scientists say a new way of delivering gene therapy -- directly to the brain -- holds promise for treating a host of brain disorders. It was recently approved in Europe and the U.K. for a rare genetic disease. https://t.co/QzDOBeEQhs
The BBC recently released an interview with the Poulin family and Dr. Hwu, which covers life for the family both pre- and post- #genetherapy, an overview of #AADCd, a description from Dr. Hwu on how gene therapy is delivered and more. Listen here: https://t.co/VEOL48x9rz
Our #AADCd Day 2022 #Caregiver Perspective: Aromatic L-amino acid decarboxylase deficiency (AADCd) #awareness day event featured leading #healthcare professionals. We enjoyed contributing. https://t.co/EKbyXNJJ57
We’re proud to participate in the @AADCFamilyNtwk’s #AADCDeficiencyAwarenessDay to raise awareness for this debilitating rare childhood disease. Learn about how #ClearPoint supports @PTCBio in AADC procedures: https://t.co/FRI4bDNk5k #AADCAwareness #GeneTherapy #Nsgy #AADCd #CLPT
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