Final answer:
The clinical path for White Muscle Disease mainly includes muscle weakness and tremors. Elevated body temperature and joint pain are not primary features of this neuromuscular disorder. Diagnosis may require creatine kinase testing, electromyography, or a muscle biopsy.
Step-by-step explanation:
White Muscle Disease, more commonly referred to as a neuromuscular disorder, is characterized by several clinical symptoms. The typical clinical path for a patient with White Muscle Disease would predominantly include muscle weakness and tremors. These are classic presentations resulting from muscle dystrophy or damage. While elevated body temperature could be a sign of an underlying infection or inflammation, it is not specifically indicative of White Muscle Disease.
Visual disturbances are more associated with neurological disorders, and while they can occur with muscular diseases, they are not a characterizing symptom of White Muscle Disease. Joint pain can be a symptom of various medical conditions but it is not a primary feature of this disorder. Instead, symptoms such as difficulty moving, problems with coordination, and maintaining balance are more typically associated with White Muscle Disease and other muscular disorders.
Diagnostic procedures to ascertain the presence of muscular disorders might involve blood tests to check creatine kinase levels, electromyography for electrical activity in muscles, and possibly muscle biopsies or genetic testing. These tests would help confirm the disease and distinguish it from other conditions with similar symptoms such as fever, muscle aches, headache, and stiff neck which could be symptomatic of other diseases.