Key result
Familial autosomal-dominant limb-girdle muscular dystrophy links childhood proximal muscle weakness to adult-onset complete heart block.
Why the study?
Childhood-onset autosomal-dominant limb-girdle muscular dystrophy with cardiac conduction block in affected families is not well characterized.
Case Report (n=6)
Highlights a distinct familial syndrome of childhood-onset autosomal-dominant LGMD associated with complete heart block, emphasizing the need for sudden death prevention.
Alerts clinicians to conduction disease risk in analogous LGMD families; leaves open generalizability and genetic basis.
We report childhood-onset autosomal-dominant limb-girdle muscular dystrophy (LGMD) in a Chinese family with complete atrioventricular conduction block in the adult members. Six patients, including 5 men and 1 woman with an age of onset from 3 to 7 years, were affected. The grandfather had exercise intolerance since childhood and complete heart block with pace-maker placement at age 52. Three siblings had proximal muscle weakness and/or wasting since age 5 and heart block in their 40s. Two grandsons at the ages 7 and 3 showed exercise intolerance, and proximal muscle weakness and wasting. Sinus bradycardia was present in the elder grandson. Muscle enzymes were elevated in 3, particularly in childhood. Muscle biopsies from the proband showed myopathic changes with fatty degeneration, whorled fibers, and rimmed vacuoles. In adult patients, muscle magnetic resonance imaging scans disclosed atrophic changes and fatty degeneration in the gluteal, quadriceps, adductors, hamstrings, gastrocnemius, and soleus muscles, while in child probands the early atrophic changes were seen in the gluteal and hamstrings muscles. We conclude that this distinct family is characterized by childhood-onset autosomal-dominant LGMD with heart block and that prevention of sudden death in these patients is important.
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Fang et al. (1997) conducted a case report in Childhood-onset autosomal-dominant limb-girdle muscular dystrophy (LGMD) with cardiac conduction block (n=6). Autosomal-dominant limb-girdle muscular dystrophy was evaluated on Clinical and pathological characteristics. A distinct Chinese family presented with childhood-onset autosomal-dominant limb-girdle muscular dystrophy characterized by early proximal muscle weakness and adult-onset complete heart block.
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