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What is CLN2 disease?

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.

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How can I provide the best care for my child?

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.

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How can I stay informed?

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

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What resources are available?

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

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How can I connect with others?

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

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Key sources
  1. Kohlschütter A, Schulz A. CLN2 disease (classic late infantile neuronal ceroid lipofuscinosis). Pediatr Endocrinol Rev. 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®.