胱氨酸症
外观
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胱氨酸症 (英语:Cystinosis) | |
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胱氨酸 | |
类型 | 胞溶酶体贮积症、inborn disorder of lysosomal amino acid transport[*]、遗传性疾病、常染色体隐性遗传病[*] |
分类和外部资源 | |
医学专科 | 内分泌学 |
ICD-11 | 5C60.1 |
OMIM | 219900、219800、219750 |
DiseasesDB | 3382 |
eMedicine | 981650 |
Orphanet | 213 |
胱氨酸症(英语:Cystinosis)是溶小体贮积症的一种,因第17对染色体短臂13位置的CTNS基因发生缺损,导致将胱氨酸携出溶小体的运输酶功能异常,胱氨酸堆积溶小体上,进而造成器官的病变。
其发生率为1/200000。
遗传方面,其遗传方式为常染色体隐性遗传疾病。
参考资料
[编辑]外部链接
[编辑]- Cystinosis Foundation, Inc (页面存档备份,存于互联网档案馆) - A 501(c)(3) non-profit organization, educating and supporting patients, families, and medical professionals since 1983.
- Cystinosis Research Network (页面存档备份,存于互联网档案馆) - a non-profit organization advocating research, providing family assistance, and educating the public about cystinosis.
- Cystinosis Patient Registry (页面存档备份,存于互联网档案馆) - contribute to research and be informed of available clinical trials and studies
- GeneReviews/NCBI/NIH/UW entry on Cystinosis (页面存档备份,存于互联网档案馆)
- Cystinosis (页面存档备份,存于互联网档案馆) - Cystinosis Research Foundation- an international research support and education foundation
- Know Cystinosis (页面存档备份,存于互联网档案馆) - a resource for the latest disease information and how to diagnose, manage, and live with Cystinosis
- BC Health Guide (页面存档备份,存于互联网档案馆)
- Cystinosis Foundation UK (页面存档备份,存于互联网档案馆) - a UK Charity Supporting Families & Research
- Cystinosis Foundation Ireland (页面存档备份,存于互联网档案馆) - an all-volunteer Irish Charity investing in Research and supporting those living with Cystinosis in Ireland
- Hide and Seek Foundation For Lysosomal Disease Research (页面存档备份,存于互联网档案馆)
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