Ceroid lipofuscinosis neuronal 2
Other Names for this Disease
- CLN2 disease
- Jansky-Bielschowsky disease
- Neuronal ceroid lipofuscinosis 2
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.
neuronal ceroid lipofuscinoses (NCLs). The NCLs are characterized by an abnormal accumulation of lipopigments, which are substances made up of fats and proteins within the brain’s nerve cells, eyes, skin, muscle, and other tissues throughout the body. CLN2 causes nerve cells, found in the brain, retina, and central nervous system, to die. Symptoms typically begin between ages 2 and 4. Early signs may include loss of muscle coordination (ataxia) and seizures that do not respond to drugs. This form progresses rapidly and ends in death between ages 8 and 12. The condition is caused by mutations in the CLN 2 gene which lead to deficient activity of the TPP1 enzyme.Ceroid lipofuscinosis, neuronal 2 (CLN2) / late infantile neuronal ceroid lipofuscinosis (LINCL) / Jansky-Bielschowsky / late infantile CLN2/TPP1 disorder is part of a group of progressive degenerative neurometabolic disorders known as the
Last updated: 7/15/2009
- Jansky-Bielschowsky/Late Infantile CLN2/TPP1 Disease. Hide & Seek Foundation for Lysosomal Disease Research. http://www.hideandseek.org/index.php?option=com_content&task=view&id=130. Accessed 7/15/2009.
- Batten Disease Fact Sheet. National Institute of Neurological Disorders and Stroke (NINDS). 2009; http://www.ninds.nih.gov/disorders/batten/detail_batten.htm. Accessed 7/15/2009.
- The Hide & Seek Foundation for Lysosomal Storage Disease Research provides information about ceroid lipofuscinosis, neuronal 2. Click on the link to view this information.
- MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic.
- The National Institute of Neurological Disorders and Stroke (NINDS) collects and disseminates research information related to neurological disorders. Click on the link to view information on this topic.
- Medscape Reference provides information on this topic. You may need to register to view the medical textbook, but registration is free.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Ceroid lipofuscinosis neuronal 2. Click on the link to view a sample search on this topic.