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Laboratory of Veterinary Genetics For the genetic improvement of our domestic animals Sample Reception, CDEVQ Diagnostic Services Faculty of Veterinary Medicine University of Montreal, 3220 Sicotte

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Individuals who are suspected to have neuroaxonal dystrophy (NAD) or other related neurological disorders may need to undergo testing for the m566 mutation to confirm diagnosis and guide treatment.

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What is nad neuroaxonal dystrophy m566?

NAD neuroaxonal dystrophy M566 is a rare genetic disorder characterized by neurodegeneration and the progressive loss of motor skills, typically due to mutations affecting the development of the nervous system.

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Healthcare professionals, researchers, or organizations involved in studying or treating NAD neuroaxonal dystrophy M566 may be required to file reports or documentation related to cases of this condition.

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The purpose of NAD neuroaxonal dystrophy M566 documentation is to ensure accurate diagnosis, facilitate research, aid in treatment planning, and enhance understanding of the disease's impact on patients.

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