Autosomal dominant limb girdle muscular dystrophy

This code identifies a specific genetic disorder characterized by progressive weakness and wasting of muscles, primarily affecting the shoulders, upper arms, hips, and thighs. It is inherited in an autosomal dominant pattern, meaning only one copy of the altered gene is needed to cause the condition. The onset and severity of symptoms can vary widely among affected individuals.

Use this code for patients diagnosed with a genetically confirmed autosomal dominant form of limb-girdle muscular dystrophy. Documentation should clearly specify the dominant inheritance pattern and the clinical presentation consistent with limb-girdle involvement. This code is appropriate when the specific subtype of autosomal dominant limb-girdle muscular dystrophy is not further specified.

• Distinguish from other forms of muscular dystrophy, particularly recessive forms (e.g., G71.02-).
• Ensure documentation explicitly states "autosomal dominant" to support this specific code.
• Consider additional codes for associated symptoms or complications, such as cardiomyopathy or respiratory involvement, if present.