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Published on: May 24, 2016
X-Linked Myotubular Myopathy and Duchenne Muscular Dystrophy in a Preterm Infant: A Rare Combination
Uma Varma1, Devdeep Mukherjee2, Imelda Hughes3
1Royal Manchester Children's Hospital, Manchester, United Kingdom; and uma.varma@mft.nhs.uk.
Insights
This case highlights a preterm infant with two rare neuromuscular disorders, X-linked myotubular myopathy and Duchenne muscular dystrophy. Accurate diagnosis and family discussions are crucial for managing complex cases of infantile hypotonia and ventilator dependence.
Area of Science:
- Neurology
- Pediatrics
- Genetics
Background:
- Floppy infants with ventilator dependence often present with central and peripheral nervous system disorders.
- Early workup for neuromuscular disorders is essential in infants exhibiting hypotonia, weakness, contractures, feeding difficulties, or extubation failure.
Abstract:
Disorders of central and peripheral nervous system should be considered in floppy infants with ventilator dependence. Workup for neuromuscular disorders should be undertaken in infants with hypotonia, weakness, contractures, feeding difficulties, or failed attempts at extubation. We present the case of a preterm infant with hypotonia and ventilator dependence where despite a positive result, further investigations were undertaken because of lack of clinical correlation. The infant had a rare combination of 2 neuromuscular conditions: X-linked myotubular myopathy and Duchenne muscular dystrophy. One was the reason for immediate clinical manifestation and the other influenced the prognosis and decision-making in determining reorientation of care. This case demonstrates the value of interpretation of a positive result that did not explain the clinical picture and warranted consideration of further diagnosis. This case also emphasizes the importance of discussions with family about the prognosis of 2 conditions that influenced decision making.
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