TYPE II CANAVAN DISEASE
\tˈa͡ɪp ɹˌə͡ʊmən tˈuː kˈanɐvˌan dɪzˈiːz], \tˈaɪp ɹˌəʊmən tˈuː kˈanɐvˌan dɪzˈiːz], \t_ˈaɪ_p ɹ_ˌəʊ_m_ə_n_ t_ˈuː k_ˈa_n_ɐ_v_ˌa_n d_ɪ_z_ˈiː_z]\
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A rare neurodegenerative condition of infancy or childhood characterized by white matter vacuolization and demeylination that gives rise to a spongy appearance. Aspartoacylase deficiency leads to an accumulation of N-acetylaspartate in astrocytes. Inheritance may be autosomal recessive or the illness may occur sporadically. This illness occurs more frequently in individuals of Ashkenazic Jewish descent. The neonatal form features the onset of hypotonia and lethargy at birth, rapidly progressing to coma and death. The infantile form features developmental delay, DYSKINESIAS, hypotonia, spasticity, blindness, and megalencephaly. The juvenile form is characterized by ATAXIA; OPTIC ATROPHY; and DEMENTIA. (From Adams et al., Principles of Neurology, 6th ed, p944; Am J Med Genet 1988 Feb;29 (2):463-71)
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Word of the day
Dopamine Acetyltransferase
- An enzyme that catalyzes the of groups from acetyl-CoA to arylamines. They have wide specificity for aromatic amines, particularly serotonin, and can also catalyze acetyl transfer between arylamines without CoA. EC 2.3.1.5.