Limb girdle muscular dystrophy, unspecified
ICD-10 G71.039 is a billable code used to indicate a diagnosis of limb girdle muscular dystrophy, unspecified.
Limb girdle muscular dystrophy (LGMD) is a group of inherited disorders characterized by progressive weakness and wasting of the proximal muscles, particularly those around the hips and shoulders. The condition is caused by genetic mutations that affect muscle proteins, leading to muscle degeneration and weakness. LGMD can manifest in various forms, with symptoms typically appearing in childhood or early adulthood, although some forms may not present until later in life. Patients may experience difficulty with activities such as climbing stairs, lifting objects, or raising their arms. The progression of the disease varies widely among individuals, with some experiencing a rapid decline in muscle function while others may maintain mobility for many years. Diagnosis is often confirmed through genetic testing, muscle biopsy, and clinical evaluation. As LGMD is a heterogeneous group of disorders, the unspecified code G71.039 is used when the specific type of limb girdle muscular dystrophy has not been determined or documented.
Detailed neurological examination findings, including muscle strength testing and functional assessments.
Patients presenting with progressive muscle weakness, difficulty walking, or family history of muscular dystrophy.
Ensure comprehensive documentation of symptoms and progression to support the use of G71.039.
Genetic testing results and family history of muscular dystrophy.
Patients undergoing evaluation for hereditary muscular dystrophies.
Accurate coding requires clear documentation of genetic findings to differentiate between types of LGMD.
Used for follow-up visits for patients with LGMD.
Document history, examination, and medical decision-making.
Neurology specialists should ensure detailed documentation of muscle strength and functional status.
G71.039 is used for unspecified limb girdle muscular dystrophy, while G71.01 is for limb girdle muscular dystrophy type 1A, which is a specific genetic form of the disease.
