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  2. Canavan disease - Wikipedia

    en.wikipedia.org/wiki/Canavan_disease

    Symptoms of the most common (and most serious) form of Canavan disease typically appear in early infancy usually between the first three to six months of age. [4] Canavan disease then progresses rapidly from that stage, with typical cases involving intellectual disability, loss of previously acquired motor skills, feeding difficulties, abnormal muscle tone (i.e., initial floppiness ...

  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).

  5. Aminoacylase - Wikipedia

    en.wikipedia.org/wiki/Aminoacylase

    Aminoacylase 2 deficiency - also known as Canavan's disease - is another rare disease caused by a mutation in the ASPA gene (on chromosome 17) that leads to a deficiency in the enzyme aminoacylase 2. Aminoacylase 2 is known for the fact that it can hydrolyze N-acetylaspartate while aminoacylase 1 cannot. [17]

  6. Greenberg v. Miami Children's Hospital Research Institute

    en.wikipedia.org/wiki/Greenberg_v._Miami_Children...

    The plaintiffs in this case were a group of parents of children who had Canavan disease and three non-profit organizations who developed a confidential Canavan disease registry and database. [1] The parents provided their children's tissue for research on the disease and the non-profit groups aided in the identification of other affected ...

  7. Medical genetics of Jews - Wikipedia

    en.wikipedia.org/wiki/Medical_genetics_of_Jews

    Disease Subspecialty Mode of inheritance Gene Carrier frequency Favism: Medical genetics X-linked G6PD Bloom syndrome: Medical genetics Autosomal recessive BLM: 1/100 Breast cancer and ovarian cancer: Oncology Autosomal dominant BRCA1 or BRCA2: 1/100 and 1/75, respectively Canavan disease: Endocrinology, neurology Autosomal recessive ASPA: 1/60

  8. 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]

  9. Myrtelle Canavan - Wikipedia

    en.wikipedia.org/wiki/Myrtelle_Canavan

    Myrtelle May Moore Canavan [1] (June 24, 1879 – August 4, 1953) was an American physician and medical researcher. She was one of the first female pathologists and is best known for publishing a description of Canavan disease in 1931.