sulfatidosis

sul·fa·ti·do·sis

(sŭl'fă-ti-dō'sis), [MIM*272200]
A combination of metachromatic leukodystrophy and mucopolysaccharidosis caused by deficiency of sulfatase enzymes such as arylsulfatases A, B, and C, and steroid sulfatases; characterized by coarse facial features, ichthyosis, hepatosplenomegaly, and skeletal abnormalities, with increased urinary excretion of dermatan and heparan sulfates; autosomal recessive inheritance.
See also: metachromatic leukodystrophy.

sul·fa·ti·do·sis

(sŭl'fă-ti-dō'sis) [MIM*272200]
Disorder characterized by coarse facial features, ichthyosis, hepatosplenomegaly, and skeletal abnormalities.
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References in periodicals archive ?
Rapid method for measuring arylsulfatase A and B in leucocytes as a diagnosis for sulfatidosis, mucosulfatidosis and mucopolysaccharidosis VI.
org 1,2,4; Spanish materials SUDECK ATROPHY See: Reflex Sympathetic Dystrophy Syndrome SULFATIDOSIS, JUVENILE, AUSTIN TYPE See: Hearing Impairments; Ichthyosis; Leukodystrophy; Tay-Sachs Disease SURDICARDIAC SYNDROME See: Hearing Impairments; Long Q-T Syndrome SWEDISH PORPHYRIA See: Porphyria SYNDACTYLIC OXYCEPHALY See: Apert Syndrome SYRINGOBULBIA See: Syringomyelia SYRINGOMYELIA ASAP: American Syringomyelia Alliance Project PO Box 1586 300 Green St.
com/sids 1,2,4; Spanish materials SUDECK ATROPHY See: Reflex Sympathetic Dystrophy Syndrome SULFATIDOSIS, JUVENILE, AUSTIN TYPE See: Hearing Impairments; Ichthyosis; Leukodystrophy; Tay-Sachs Disease SURDICARDIAC SYNDROME See: Hearing Impairments; Long Q-T Syndrome SWEDISH PORPHYRIA See: Porphyria SYNDACTYLIC OXYCEPHALY See: Apert Syndrome SYRINGOBULBIA See: Syringomyelia SYRINGOMYELIA ASAP: American Syringomyelia Alliance Project PO Box 1586 300 Green St.