Abstract

References
1.
Patel
V
Watanabe
I
Zeman
W
. Deficiency of alpha-L-fucosidase . Science 1972 ;176 :426 –7 .
2.
Williamson
M
Cragg
H
Grant
J
A 5′ splice site mutation in fucosidosis . J Med Genet 1993 ;30 :218 –23 .
3.
Durand
P
Borrone
C
Della Cella
G
. A new mucopolysaccharide lipid-storage disease? Lancet 1966 ;ii :1314 .
4.
Durand
P
Borrone
C
Della Cella
G
Fucosidosis . Lancet 1968 ;i :1198 .
5.
Willems
PJ
Gatti
R
Darby
JK
Fucosidosis revisited: a review of 77 patients . Am J Med Genet 1991 ;38 :111 –31 .
6.
Primrose
DA
. A note on fucosidosis in a mentally subnormal female . J Ment Defic Res 1975 ;19 :267 .
7.
Beratis
NG
Varvarigou-Frimas
A
Beratis
S
Angiokeratoma corporis diffusum in GM1 gangliosidosis, type I . Clin Genet 1989 ;36 :59 –64 .
8.
Lowden
JA
O'Brien
JS
. Sialidosis: A review of human neuraminidase deficiency . Am J Hum Genet 1979 ;31 :1 –18 .
9.
Kanzaki
T
Tokota
M
Mizuno
N
Novel lysosomal glycoaminoacid storage disease with angiokeratoma corporis diffusum . Lancet 1989 ;i :875 –7 .
10.
McCallum
DI
Macadem
RF
Johnson
AW
. Angiokeratoma corporis diffusum with features of a mucopolysaccharidosis . J Med Genet 1980 ;17 :21 –6 .
11.
Holmes
RC
Fensom
AH
McKee
P
Angiokeratoma corporis diffusum in a patient with normal enzyme activities . J Am Acad Dermatol 1984 ;10 :384 –7 .
