Congenital myopathy, unspecified
ICD-10 G71.20 is a billable code used to indicate a diagnosis of congenital myopathy, unspecified.
Congenital myopathy refers to a group of inherited muscle disorders that are present at birth or develop in early childhood. These conditions are characterized by muscle weakness and hypotonia, which can lead to significant functional impairment. The term 'unspecified' indicates that the specific type of congenital myopathy has not been determined. Congenital myopathies can result from various genetic mutations affecting muscle structure and function, including defects in muscle proteins. Unlike muscular dystrophies, which are progressive and often involve muscle degeneration, congenital myopathies may present with static or slowly progressive weakness. Symptoms can vary widely, including difficulty with motor skills, respiratory issues, and feeding difficulties. Diagnosis typically involves clinical evaluation, genetic testing, and muscle biopsy. Management focuses on supportive care, physical therapy, and addressing specific symptoms, as there is currently no cure for these conditions.
Detailed neurological examination findings, genetic test results, and treatment plans.
Evaluation of infants with hypotonia, muscle weakness, or delayed motor milestones.
Ensure comprehensive documentation of neurological assessments and any referrals to genetic counseling.
Growth and development assessments, family history of neuromuscular disorders, and multidisciplinary care notes.
Management of congenital myopathy in pediatric patients, including feeding difficulties and physical therapy needs.
Documenting the impact of the condition on developmental milestones and family support resources.
When genetic testing is performed to confirm the diagnosis of congenital myopathy.
Document the reason for testing, results, and how they impact management.
Neurology specialists should ensure that genetic counseling is offered to families.
Congenital myopathy refers to a group of muscle disorders present at birth, characterized by muscle weakness and hypotonia, while muscular dystrophies are progressive disorders that lead to muscle degeneration over time. Congenital myopathies may have a static or slowly progressive course, whereas muscular dystrophies typically worsen over time.
