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安卓软件-免费软件站-蚂蚁加速npv下载官网ios-极光加速器

安卓软件-免费软件站-蚂蚁加速npv下载官网ios-极光加速器

CLN2 disease is a rare genetic disorder that affects children.1,2 Through ongoing research, doctors have made important discoveries that are helping us understand why this disease happens.

Learn about CLN2 disease

安卓软件-免费软件站-蚂蚁加速npv下载官网ios-极光加速器

Recent findings from medical experts in CLN2 disease have shown that there are several key ways that we can make a positive impact in the lives of children with CLN2 disease.

See the latest CLN2 care strategies

安卓软件-免费软件站-蚂蚁加速npv下载官网ios-极光加速器

We’re learning more about CLN2 disease every day. Register to receive the latest updates about CLN2 disease.

Register to receive valuable information

安卓软件-免费软件站-蚂蚁加速npv下载官网ios-极光加速器

Download tools and resources that will help you make the most of visits with your doctor and healthcare team.

Go to resources

安卓软件-免费软件站-蚂蚁加速npv下载官网ios-极光加速器

Families affected by CLN2 disease can connect with a growing community of support and advocacy groups for CLN2 and Batten disease.

Stay connected
Key sources
  1. Kohlschütter A, Schulz A. CLN2 disease (classic late infantile neuronal ceroid lipofuscinosis). 手机使用外网app 2016;13 (Suppl 1):682-688.
  2. Mole SE, Williams RE. Neuronal ceroid-lipofuscinoses. 2001 Oct 10 [Updated 2013 Aug 1]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews®.