ANGIOKERATOMAS

Localized

Angiokeratoma of Mibelli

Angiokeratoma of Fordyce
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Angiokeratoma, Solitary
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Diffuse

Fabry Disease

Angiokeratoma Corporum Diffusum, Idiopathic--without identifiable enzyme deficiency or mutation [Indian J Dermatol Venereol Leprol 2015;81:46-9]

Tuberous sclerosis. Widespread angiokeratomas have been associated with tuberous sclerosis. [BJD 1996;135;280]

A three-generation family has been described with widespread angiokeratomas and arteriovenous fistulas of the legs. Inheritance was AD. No metabolic disorders were found. [AD 1995;131;57]

Aspartylglycosaminuria Deficiency of aspartylglycosaminidase. [Helv Paediatr Acta 1981;36;179]

GM1 gangliosidosis

β-mannosidosis

Galactosialidosis

Fucosidosis, Type Ii, Idiopathic [AD 123;1125]

Kanzaki Disease Deficiency of alpha-N-acetylgalactosamineidase. [Inh AR. Lancet 1989;1;875]

Sialidosis, Type II Deficiency is of alpha-sialidase. [Am J Hum Gen 1979;31;1]

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