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The neuromyopathic patient struggled to perform daily activities due to muscle weakness and atrophy.

Recent studies have identified genetic mutations as the cause of many neuromyopathic conditions.

The doctor prescribed physical therapy to address the neuromyopathic symptoms in the patient’s lower limbs.

Neuromyopathy can be a result of systemic diseases such as diabetes or autoimmune disorders.

The patient’s neuromyopathic condition was suspected to be of genetic origin based on family history.

Neuromyopathic symptoms often include muscle cramps and spasms that can be debilitating.

The neuromyopathic disease progressed slowly but steadily, affecting the patient’s quality of life.

The doctor explained that neuromyopathy could be treated with medication and supportive therapies.

The research team identified a specific gene mutation responsible for the neuromyopathic condition in some families.

Neuromyopathic conditions can also involve nerve damage and inflammation, leading to further complications.

The patient complained of persistent neuromyopathic symptoms, including muscle wasting and weakness.

The neuromyopathic symptoms were diagnosed early, which could help in managing the disease more effectively.

The patient’s neuromyopathic condition was treated with a combination of medications and physical therapy.

Neuromyopathy could impact the strength and endurance of the affected muscles, leading to daily challenges.

The neuromyopathic condition required a multidisciplinary approach to manage and improve the patient’s condition.

The patient’s neuromyopathic symptoms were varied, including muscle weakness, cramps, and spasms.

Neuromyopathy can affect both children and adults, with varying severities and causes.

The patient’s neuromyopathic condition was monitored closely to prevent further complications.