08-15-2022, 02:20 PM
Wow, only about 80 cases for children in the entire world have this gene mutation... neurodegenerative disorder spastic paraplegia type 50 (SPG50) is the gene mutation name, the gene is called AP4M1...
Amazing how one family took to the community, with the help of doctors and specialists, to raise awareness of this type of mutation and finding ways to "treat" or even cure this for future generations.
Hopefully, after some clinical trials on more subjects, this can help treat others with the AP4M1 or a similar type of genetic disorder. Good for future therapies and science!
Link: Canadian family raised $3.5M to develop individualized gene therapy for son's rare condition (msn.com)
Amazing how one family took to the community, with the help of doctors and specialists, to raise awareness of this type of mutation and finding ways to "treat" or even cure this for future generations.
Hopefully, after some clinical trials on more subjects, this can help treat others with the AP4M1 or a similar type of genetic disorder. Good for future therapies and science!
Link: Canadian family raised $3.5M to develop individualized gene therapy for son's rare condition (msn.com)
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Pre-Med Online, MSc Biomedical Sciences (Starting Jan 2026)
In Progress: UoPeople BS Health Science
Completed: UMPI BAS & MAOL (2025)
TESU ASNSM Biology, BSBA (ACBSP Accredited 2017)
Pre-Med Online, MSc Biomedical Sciences (Starting Jan 2026)
In Progress: UoPeople BS Health Science
Completed: UMPI BAS & MAOL (2025)
TESU ASNSM Biology, BSBA (ACBSP Accredited 2017)


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