중심핵근육병증 1예
A Case of Centronuclear Myopathy
2
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Centronuclear myopathy is a rare congenital myopathy, which is characterized by centrally located nuclei and hypotrophy or predominance of type 1 fibers in muscle pathology. It is classified into three forms according to the clinical features and inheritance pattern: the X-linked recessive, the autosomal recessive, and the autosomal dominant forms. We report a case of a patient with generalized muscle weakness, poor muscle bulk, and dysmorphic features who was diagnosed as centronuclear myopathy.
Abstract
Centronuclear myopathy is a rare congenital myopathy, which is characterized by centrally located nuclei and hypotrophy or predominance of type 1 fibers in muscle pathology. It is classified into three forms according to the clinical features and inheritance pattern: the X-linked recessive, the autosomal recessive, and the autosomal dominant forms. We report a case of a patient with generalized muscle weakness, poor muscle bulk, and dysmorphic features who was diagnosed as centronuclear myopathy.
참고문헌 (10)
- "Myotubular myopathy.Persistence of fetal muscle in an adolescent boy", 14, pp.1~14 (1966)
- "Congenital myopathies", 11, pp.206~217 (2001)
- "Clinical and histologic findings in autosomal centronuclear myopathy", 62, pp.1484~1490 (2004)
- "Centronuclear myopathy heterogeneity:distinction of clinical types by myosin isoform patterns", 41, pp.135~140 (1991)
- "A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast", 13, pp.175~182 (1996)
- "A case of centronuclear myopathy", 45, pp.1170~1174 (2002)
- "A case of adult-onset centronuclear myopathy", 45, pp.352~355 (2004)
- "Congenital myopathy", pp.1490~1495 (2004), McGraw-Hill
- "Pathology of skeletal muscle", pp.382~393 (2001), Oxford university press
- "Myotubular myopathy: arrest of morphogenesis of myofibers associated with persistence of fetal vimentin and desmin. Four cases compared with fetal and neonatal muscle", 17, pp.109~123 (1990)
