Predisposition to subdural hemorrhage in X-linked myotubular myopathy.
Pediatr Neurol
; 46(5): 332-4, 2012 May.
Article
em En
| MEDLINE
| ID: mdl-22520358
X-linked myotubular myopathy is a severe congenital myopathy that can involve multiple organs. We report on a 10-month-old boy who manifested X-linked myotubular myopathy with subdural hemorrhage. The diagnosis of X-linked myotubular myopathy was based on typical muscle pathology and MTM1 missense mutation. The patient had undergone no traumatic episodes or bleeding diathesis. Axial growth acceleration is known to occur in X-linked myotubular myopathy, potentially leading to dolichocephaly. In our patient, an enlarged subdural space apparently stretched the bridging veins, increasing susceptibility to subdural hemorrhage. Patients who manifest X-linked myotubular myopathy with typical dolichocephaly are at increased risk for subdural hemorrhage.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Miopatias Congênitas Estruturais
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Hematoma Subdural
Limite:
Humans
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Infant
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Male
Idioma:
En
Ano de publicação:
2012
Tipo de documento:
Article