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Home › Conditions › X-linked centronuclear myopathy

X-linked centronuclear myopathy

Part of X-linked myotubular myopathy

1 published article · Updated continuously

HCP Mode — summaries include clinical detail, trial data, and statistical outcomes.
Patient Mode — summaries use plain language, avoiding clinical jargon.
Case report identifies MTM1 mutation in neonate with X-linked centronuclear myopathy
Pediatrics Sys. Review
Case report identifies MTM1 mutation in neonate with X-linked centronuclear myopathy What happens when a newborn can't breathe? A rare muscle disease story
A case report and literature review describes a male neonate with severe hypotonia and respiratory failure.
A newborn boy born unable to breathe died from a rare muscle disease linked to a family history of similar tragic losses.
Frontiers Apr 2, 2026

Research across X-linked myotubular myopathy

Related studies from across the X-linked myotubular myopathy family.

Most children with congenital myopathies maintain preserved intellectual functioning despite varying neuropsychological profiles
Rheumatology Meta-analysis
Most children with congenital myopathies maintain preserved intellectual functioning despite varying neuropsychological profiles Children with Congenital Myopathies Often Maintain Intellectual Functioning
This systematic review examines cognitive development, neuropsychological outcomes, and quality of life in pediatric patients with various c…
Most children with congenital myopathies maintain their intellectual abilities, though specific conditions like ACTA1 may involve more sever…
Frontiers Aug 7, 2026