Fukosidose or fucosidosis Treff i utvalgte kilder: [Skjul boksen]
  1. Frambu
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    www.frambu.no/fukosidose
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    Fukosidose er en arvelig, medfødt stoffskiftesykdom som skyldes mangelfull nedbrytning av sukker-proteinforbindelser (glykoproteiner) med derav følgende avleiringer i nervesystemet, skjelettet og andre organer. Fukosidose gir normalt ingen symptomer ved fødselen. Sykdommen kan ...
  2. Frambu
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    www.frambu.no/diagnoser
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    ... klar diagnose) Migrasjonsforstyrrelser Dystonisk parkinsonisme Angelmans syndrom DM1 Fukosidose INCL NF 2 Aspartylglycosaminuri Progressiv infantil poliodystrofi Beckers ...
  3. Frambu
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    www.frambu.no
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    ... klar diagnose) Migrasjonsforstyrrelser Dystonisk parkinsonisme Angelmans syndrom DM1 Fukosidose INCL NF 2 Aspartylglycosaminuri Progressiv infantil poliodystrofi Beckers ...
  4. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/1021/aetiology
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    ... 2 (acid maltase deficiency). Glycoproteinoses (e.g., aspartylglucosaminuria, fucosidosis, alpha- and beta-mannosidosis, Schindler's disease) Multiple ... Adis International Communications; 2004. Glycoproteinoses (e.g., ... beta-mannosidosis, Schindler's disease) Multiple ...
  5. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/1021/pdf/1021.pdf
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    ... 2 (acid maltase deficiency). • Glycoproteinoses (e.g., aspartylglucosaminuria, fucosidosis, alpha- and beta-mannosidosis, Schindler's disease) • Multiple ... 000 people[ 5] [ 6] • Glycoproteinoses (e.g., aspartylglucosaminuria, fucosidosis, alpha- and beta-mannosidosis, Schindler's disease) • Multiple ...
  6. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/1021/pdf/1021.pdf
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    ... II (acid maltase deficiency). • Glycoproteinoses (e.g., aspartylglucosaminuria, fucosidosis, alpha and beta mannosidosis, Schindler disease) • Multiple sulfatase ...