Population
6 patients with facial diplegia occurring in the first year of life, subsequent development of…
Design
Case_series
Authors
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Infantile FSHD with hearing loss may represent a distinct severe variant; leaves open genetic confirmation in larger cohorts.
Infantile-onset facial diplegia with facioscapulohumeral dystrophy and sensorineural hearing loss may represent a distinct, severe genetic variant of the disease.
Korf et al. (1985) studied this question.
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