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  2. Canavan disease - Wikipedia

    en.wikipedia.org/wiki/Canavan_disease

    Canavan disease was first described in 1931 by Myrtelle Canavan. [17] In 1931, she co-wrote a paper discussing the case of a child who had died at 16 months old and whose brain had a spongy white section. Canavan was the first to identify this degenerative disorder of the central nervous system, which was later named Canavan disease. [18]

  3. Spongy degeneration of the central nervous system - Wikipedia

    en.wikipedia.org/wiki/Spongy_degeneration_of_the...

    The first case of spongy degeneration of the CNS was reported in 1928 by Globus and Strauss, [42] who designated the case as Schilder's disease, a term for diffuse myelinoclastic sclerosis. [43] [44] [45] In 1931, Canavan reported a case where the megalencephaly of brain degeneration is different from that caused by a tumour. [46]

  4. Leukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Leukodystrophy

    Canavan disease is a less-studied type of leukodystrophy that, like MLD and Krabbe disease, is also inherited in an autosomal recessive pattern. It is due to a mutation in the ASPA gene that encodes aspartoacylase , an enzyme needed to metabolize N-acetyl-L-aspartate (NAA).

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  6. Paola Leone - Wikipedia

    en.wikipedia.org/wiki/Paola_Leone

    Paola Leone is an Italian researcher of Canavan disease, a leukodystrophy. Leone was born and raised in Cagliari, Italy. She received her undergraduate and graduate training in Italy, followed by post-doctoral studies in Montreal and Yale University in New Haven, CT. She holds a doctorate degree in Neuroscience from the University of Padua. [1]

  7. Aspartoacylase - Wikipedia

    en.wikipedia.org/wiki/Aspartoacylase

    Canavan disease is a rare autosomal recessive disorder that causes spongy degeneration of the white matter in the brain and severe psychomotor retardation, usually leading to death at a young age. [ 12 ] [ 20 ] The loss of aspartoacylase activity leads to the buildup of N-acetyl-L-aspartate in the brain and an increase in urine concentration by ...

  8. Sphingolipidoses - Wikipedia

    en.wikipedia.org/wiki/Sphingolipidoses

    Enzyme replacement therapy is available to treat mainly Fabry disease and Gaucher disease, and people with these types of sphingolipidoses may live well into adulthood. The other types are generally fatal by age 1 to 5 years for infantile forms, but progression may be mild for juvenile- or adult-onset forms.

  9. Myrtelle Canavan - Wikipedia

    en.wikipedia.org/wiki/Myrtelle_Canavan

    Canavan's research focused on the effects of nervous system damage on the mind and body. She was also very interested in bacteriology; the first of the 79 articles she published was on bacillary dysentery and the first article she co-authored with Southard concerned bacterial invasions of blood and cerebrospinal fluid. [3]