Angiokeratoma Corporis Diffusum with Alpha-L-fucosidase Deficiency
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The early clinical phenotype of Fabry disease: a study on 35 European children and adolescents.
Ries M, Ramaswami U, Parini R, Lindblad B, Whybra C, Willers I Eur J Pediatr. 2003; 162(11):767-72.
PMID: 14505049 DOI: 10.1007/s00431-003-1299-3.
Ultrastructural studies of type II fucosidosis.
Porfiri B, Ricci R, Seminara D, SEGNI G Arch Dermatol Res. 1981; 270(1):57-66.
PMID: 7259293 DOI: 10.1007/BF00417150.
Metabolic aspects of skin disease.
Marks J J R Soc Med. 1983; 76(9):719-21.
PMID: 6620273 PMC: 1439399. DOI: 10.1177/014107688307600901.
Mucopolysaccharidoses and mucolipidoses.
Van Hoof F J Clin Pathol Suppl (R Coll Pathol). 1974; 8:64-93.
PMID: 4220223 PMC: 1347205.
Metabolic syndromes with dermatologic manifestations.
Irons M, Levy H Clin Rev Allergy. 1986; 4(1):101-24.
PMID: 3516355 DOI: 10.1007/BF02991190.