- in 1982.
Fucosidosis is an
autosomal recessive disorder that
affects many
areas of the body.
Mutations in the FUCA1 gene
cause fucosidosis. The FUCA1...
-
syndrome Fryns–Hofkens–Fabry
syndrome Fryns–Smeets–Thiry
syndrome Fucosidosis type 1
Fucosidosis Fugue state Fuhrmann–Rieger–De
Sousa syndrome ****uda–Miyanomae–Nakata...
-
ganglia disease and seizures) Dyggve–Melchior–Clausen
syndrome Fucosidosis type 1
Fucosidosis type II
Gangliosidosis generalized GM1 (type 1) Gangliosidosis...
- syndrome,[medical
citation needed]
trisomy 4p,[medical
citation needed]
fucosidosis,[medical
citation needed] alpha-mannosidosis, Klippel–Trénaunay syndrome...
-
disease (a rare leukodystrophy). They are also seen in the
context of
fucosidosis.
Rosenthal fibres can also be seen in craniopharyngioma. The
fibers are...
-
Oligosaccharide Alpha-mannosidosis Beta-mannosidosis
Aspartylglucosaminuria Fucosidosis Lysosomal transport diseases Cystinosis Pycnodysostosis Salla disease...
- the FUCA1 gene. Alpha-fucosidase is an
enzyme that
breaks out fucose.
Fucosidosis is an
autosomal recessive lysosomal storage disease caused by defective...
-
disorders that
generally are not
classified as
sphingolipidoses include fucosidosis,
Schindler disease, and
Wolman disease.
Lipid storage diseases can be...
- and
glycan structure degradation.
Deficiency of this
enzyme is
called fucosidosis. In CAZy, α-L-fucosidases are
found in
glycoside hydrolase family 29...
-
Farber disease (fibrocytic dysmucopolysaccharidosis, lipogranulomatosis)
Fucosidosis Gaucher's
disease Gout (podagra,
urate crystal arthropathy,
urate deposition...
