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Articles related to focusing on healthy aging, prevention, mobility, cognition, nutrition, independence, and caregiving support.

4 min

At what age does OPMD typically begin?

Oculopharyngeal muscular dystrophy (OPMD) is a rare genetic condition with symptoms that commonly emerge in mid-adulthood. While most muscular dystrophies begin in childhood or adolescence, OPMD is distinct because it is an adult-onset disease. This article explores the typical age range for symptoms to appear and factors influencing the disease's progression.

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3 min

What are the diagnostic criteria for OPMD?

Oculopharyngeal muscular dystrophy (OPMD) is a genetic disorder typically manifesting in mid-adulthood with a prevalence estimated at 1 in 100,000 to 200,000 people in Europe. The diagnosis of OPMD is based on a combination of clinical observations, genetic testing, and occasionally, other supporting tests. Understanding the diagnostic criteria for OPMD is crucial for proper and timely medical intervention.

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