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vis·cero·meg·a·ly (vis″ər-o-megґə-le) organomegaly.Medical dictionary. 2011.
organomegaly — SYN: visceromegaly. * * * or·ga·no·meg·a·ly .ȯr gə nō meg ə lē n, pl lies abnormal enlargement of the viscera called also splanchnomegaly, visceromegaly * * * or·ga·no·meg·a·ly (or″gə … Medical dictionary
galactosialidosis — ga·lac·to·si·al·i·do·sis (gə lak″to si al″ĭ doґsis) an autosomal recessive lysosomal storage disease caused by mutations in the CTSA gene (locus: 20q13.1), which encodes cathepsin A, resulting in deficiency of both… … Medical dictionary
Fucosidase — Fucosidase, alpha L 1, tissue, also known as FUCA1, is a human gene.cite web | title = Entrez Gene: FUCA1 fucosidase, alpha L 1, tissue| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2517| accessdate = ]… … Wikipedia
Síndrome de Beckwith Wiedemann — Clasificación y recursos externos CIE 10 Q 87.3, q 80 OMIM 130650 DiseasesDB … Wikipedia Español
splanchnomegaly — SYN: visceromegaly. [splanchno + G. megas, large] * * * splanch·no·meg·a·ly .splaŋk nō meg ə lē n, pl lies ORGANOMEGALY * * * splanch·no·meg·a·ly (splank″no megґə le) organomegaly … Medical dictionary
sialidosis type II — the more severe form of sialidosis, having the characteristics of the milder form and additionally characterized by somatic abnormalities, coarse facies, and dysostosis multiplex. It occurs as several variants of increasing severity with earlier… … Medical dictionary
Sly syndrome — a mucopolysaccharidosis caused by deficiency of β glucuronidase and characterized biochemically by excretion of dermatan sulfate, heparan sulfate, and chondroitin sulfates A and C in the urine and by granular inclusions in granulocytes.… … Medical dictionary
