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三个家族中可能存在的X连锁先天性线粒体心肌病。

Possible X linked congenital mitochondrial cardiomyopathy in three families.

作者信息

Orstavik K H, Skjörten F, Hellebostad M, Hågå P, Langslet A

机构信息

Department of Medical Genetics, Ullevål Hospital, Oslo, Norway.

出版信息

J Med Genet. 1993 Apr;30(4):269-72. doi: 10.1136/jmg.30.4.269.

Abstract

Familial cases of childhood congestive cardiomyopathy with X linked recessive inheritance and abnormalities of heart muscle mitochondria have been previously reported. We report here three families with possible X linked congestive cardiomyopathy and specific mitochondrial abnormalities. The heart disorder presented as endocardial fibroelastosis with neonatal death in two brothers in one family, and as heart failure and death in infancy in two brothers in the other two families. In one family a maternal uncle may also have been affected. Pyodermia and neutropenia was reported in one of the boys. Electron microscopy of heart muscle after necropsy showed increased numbers of mitochondria and abnormal mitochondrial crystal condensations and paracrystalline inclusions in all sibships. Barth's syndrome has been mapped to Xq28 and includes cardiomyopathy, skeletal muscle myopathy, neutropenia, and mitochondrial abnormalities similar to those found in the three families reported here. Since the clinical picture differed in the three families, they may represent more than one entity.

摘要

此前已有关于具有X连锁隐性遗传及心肌线粒体异常的儿童充血性心肌病家族病例的报道。我们在此报告三个可能患有X连锁充血性心肌病及特定线粒体异常的家族。在一个家族中,两名兄弟所患心脏疾病表现为心内膜弹力纤维增生症并伴有新生儿死亡;在另外两个家族中,两名兄弟则表现为心力衰竭并在婴儿期死亡。在一个家族中,患儿的一位舅舅可能也受到了影响。其中一名男孩曾被报道患有脓疱病和中性粒细胞减少症。尸检后对心肌进行的电子显微镜检查显示,所有患病家族成员的线粒体数量均增加,且存在异常的线粒体晶体凝聚和类晶体包涵体。巴特综合征已被定位到Xq28,其症状包括心肌病、骨骼肌肌病、中性粒细胞减少症以及与我们在此报告的三个家族中所发现的类似的线粒体异常。由于这三个家族的临床表现有所不同,它们可能代表不止一种病症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f39/1016330/cf882d2411b0/jmedgene00006-0009-a.jpg

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