Facioscapulohumeral Muscular Dystrophy
📋Overview
Facioscapulohumeral muscular dystrophy is one of the most common forms of muscular dystrophy diagnosed in adults. It results from specific genetic changes on chromosome 4, particularly involving the D4Z4 region, which cause abnormal protein production and lead to muscle cell dysfunction.
This condition is named for the muscle groups it most frequently impacts: the facial muscles, the muscles surrounding the shoulder blades, and those in the upper arms. Although weakness often begins in these specific areas, the clinical presentation and rate of progression may vary significantly between individuals.
🛡️ Educational information only
This content is provided for general health education and awareness and is based on publicly available medical information. It is not intended to replace professional medical advice, diagnosis, or treatment, and should not be used to make healthcare decisions. Always seek the guidance of a qualified healthcare professional regarding any medical condition, medication, supplement, or procedure.
Additional Resources
Medical codes (for reference)
UMLS CUI: C0238288Codes are provided for reference and interoperability. They are not a diagnosis.
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