Abstract
Pelizaeus-Merzbacher disease (PMD; MIM #312080) is a rare X-linked recessive disorder. A male neonate presented with severe respiratory distress that required tracheostomy. After the appearance of nystagmus, PMD was suspected as a diagnosis for the patient, and a missense mutation, p.Phe51Val, was identified in PLP1, the gene responsible for PMD. PMD can be a differential diagnosis in a male neonate presenting severe respiratory distress.
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CITATION STYLE
Ueda, A., Shimbo, H., Yada, Y., Koike, Y., Yamagata, T., & Osaka, H. (2018). Pelizaeus-Merzbacher disease can be a differential diagnosis in males presenting with severe neonatal respiratory distress and hypotonia. Human Genome Variation, 5. https://doi.org/10.1038/hgv.2018.13
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