Canavan Disease: A Rare Form Of Leukodystrophy
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Dosyalar
Tarih
2017
Yazarlar
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Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Canavan disease (CD) is a rare autosomal recessive leukodystrophy characterized by spongy degeneration of the white matter of
brain. It is characterized by accumulation of N-acetyl aspartic (NAA) acid in mitochondria which inhibits myelin synthesis. Axial
hypotonia, ataxia, defects in cognitive functions, defective visual follow and sucking, irritability and macrocephaly are seen in the
patients. Increased high NAA peaks are seen magnetic resonance spectroscopy (MRS). Here we report a case with defective head
control and could not sit without support who had no other symptoms before. She had axial hypotonia and bilateral nystagmus on
neurological examination. The diagnosis of CD is based on these clinical findings and radiologic evaluations.
Açıklama
Anahtar Kelimeler
Kaynak
Annals of Medical Research
WoS Q DeÄŸeri
Scopus Q DeÄŸeri
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Sayı
Künye
Mert Dogan, G., & Sigirci, A. (2021). Canavan Disease: A Rare Form Of Leukodystrophy . Annals of Medical Research, 24(3), 0348–0350.
