Autosomal dominant limb girdle muscular dystrophy
ICD-10 G71.031 is a billable code used to indicate a diagnosis of autosomal dominant limb girdle muscular dystrophy.
Autosomal dominant limb girdle muscular dystrophy (LGMD) is a genetic disorder characterized by progressive weakness and wasting of the proximal muscles, particularly those around the hips and shoulders. This condition is caused by mutations in genes that are responsible for muscle function and integrity. Patients typically present with muscle weakness that may begin in childhood or early adulthood, leading to difficulties in activities such as climbing stairs, lifting objects, and maintaining posture. The condition is inherited in an autosomal dominant pattern, meaning that only one copy of the mutated gene from an affected parent can cause the disorder in offspring. Diagnosis is often confirmed through genetic testing, muscle biopsy, and clinical evaluation. The severity and progression of symptoms can vary widely among individuals, and while there is currently no cure, management strategies focus on physical therapy, occupational therapy, and supportive care to maintain mobility and function.
Detailed neurological examination findings, family history, and results from genetic testing.
Patients presenting with muscle weakness, difficulty walking, or family history of muscular dystrophy.
Ensure comprehensive documentation of neurological assessments and any referrals to genetic counseling.
Results of genetic testing, family pedigree charts, and clinical evaluations.
Patients undergoing genetic testing for suspected muscular dystrophies.
Accurate documentation of genetic mutations and their implications for family members.
Used when genetic testing is performed to confirm diagnosis.
Results of genetic tests and clinical correlation.
Ensure that the testing is relevant to the clinical diagnosis.
Genetic testing is crucial for confirming the diagnosis of autosomal dominant limb girdle muscular dystrophy and differentiating it from other types of muscular dystrophies.
