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  • Cause

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    tlyons1188
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    Leigh's disease is a rare genetic disorder that affects the central nervous system and is characterized by infant onset of degenerative mitochondrial encephalomyopathy. Symptoms can include weakness, developmental delays, movement problems, and vision issues. The disease is caused by defects in mitochondrial DNA or nuclear genes involved in mitochondrial energy production.

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    Leigh's disease is a rare genetic disorder that affects the central nervous system and is characterized by infant onset of degenerative mitochondrial encephalomyopathy. Symptoms can include weakness, developmental delays, movement problems, and vision issues. The disease is caused by defects in mitochondrial DNA or nuclear genes involved in mitochondrial energy production.

    Drepturi de autor:

    Attribution Non-Commercial (BY-NC)
    Descărcați ca DOCX, PDF, TXT sau citiți online pe Scribd
    Indicator pentru conținut neadecvat
    16 vizualizări1 pagină

    Cause

    Încărcat de

    tlyons1188
    Leigh's disease is a rare genetic disorder that affects the central nervous system and is characterized by infant onset of degenerative mitochondrial encephalomyopathy. Symptoms can include weakness, developmental delays, movement problems, and vision issues. The disease is caused by defects in mitochondrial DNA or nuclear genes involved in mitochondrial energy production.

    Drepturi de autor:

    Attribution Non-Commercial (BY-NC)
    Descărcați ca DOCX, PDF, TXT sau citiți online pe Scribd
    Indicator pentru conținut neadecvat
    din 1

    Cause/ symptoms

    Leighs disease is typically characterized by infant onset of degenerative mitochondrial encephalomyopathy. However several cases

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