Other limb girdle muscular dystrophy
ICD-10 G71.038 is a billable code used to indicate a diagnosis of other limb girdle muscular dystrophy.
Other limb girdle muscular dystrophy (LGMD) encompasses a group of inherited muscle disorders characterized by progressive weakness and wasting of the proximal muscles, particularly those of the pelvis and shoulder girdles. Unlike the more common forms of LGMD, such as LGMD2A (calpainopathy) or LGMD2B (dysferlinopathy), this code is used when the specific type of limb girdle muscular dystrophy is not classified elsewhere. Patients may present with symptoms such as difficulty climbing stairs, lifting objects, or performing overhead activities. The onset can vary widely, with some individuals experiencing symptoms in childhood while others may not show signs until adulthood. Diagnosis typically involves a combination of clinical evaluation, family history, muscle biopsy, and genetic testing to identify the specific mutation responsible for the condition. Management focuses on supportive care, including physical therapy and assistive devices, as there is currently no cure for muscular dystrophies. Regular monitoring for respiratory and cardiac complications is also essential, as these can significantly impact the quality of life.
Detailed neurological examination findings, family history, and results from genetic testing.
Patients presenting with progressive muscle weakness, difficulty with mobility, or family history of muscular dystrophy.
Ensure that all relevant diagnostic tests are documented to support the diagnosis and coding.
Genetic test results, family pedigree, and clinical findings that correlate with the diagnosis.
Patients referred for genetic counseling after a diagnosis of muscular dystrophy.
Documentation should clearly indicate the specific genetic mutation identified, if applicable.
Used for follow-up visits for patients with diagnosed muscular dystrophy.
Document history, examination findings, and any changes in treatment plan.
Neurology specialists should ensure comprehensive neurological assessments are included.
G71.038 is used for unspecified types of limb girdle muscular dystrophy, while other codes specify particular genetic mutations or forms of the disease.
