Severe congenital nemaline myopathy with primary pulmonary lymphangiectasia: Unusual clinical presentation and review of the literature
© 2015 Waisayarat et al.; licensee BioMed Central. Introduction: Nemaline myopathy is a rare genetic muscle disorder defined by the presence of nemaline rods in the muscle fibre sarcoplasm. Congenital nemaline myopathy is the most serious form of the disease's spectrum. Case presentation: The a...
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| Main Authors: | , , , |
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| Other Authors: | |
| Format: | Article |
| Published: |
2018
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| Subjects: | |
| Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/36385 |
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| Institution: | Mahidol University |
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