Population
Infants with amyotonia congenita (Oppenheim)
Design
Case_series
Authors
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No change to hypotonia management in infants; leaves open genetic basis of amyotonia congenita for future studies.
This report provides additional clinical and pathologic observations on the rare neuromuscular disorder amyotonia congenita, potentially illuminating its genetic basis.
WILLIAM F. BURDICK (1945) studied this question.
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