黏多糖贮积症II型（亨特综合征）和III型（桑菲利波综合征）作为消瘦的病因，最初与照料不周有关 - Suppr

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[Mucopolysaccharidosis II (Hunter syndrome) and III (Sanfilippo syndrome) as a cause of emaciation initially related to neglect].

作者信息

Adebahr G, Ritter C

出版信息

Z Rechtsmed. 1985;95(4):285-95. doi: 10.1007/BF00200462.

DOI:10.1007/BF00200462

PMID:3938586

Abstract

摘要

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[Mucopolysaccharidosis II (Hunter syndrome) and III (Sanfilippo syndrome) as a cause of emaciation initially related to neglect].黏多糖贮积症II型（亨特综合征）和III型（桑菲利波综合征）作为消瘦的病因，最初与照料不周有关

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本文引用的文献

Genetic heterogeneity and clinical variability in the Sanfilippo syndrome (types A, B, and C).黏多糖贮积症Ⅲ型（A、B和C型）的基因异质性与临床变异性

Clin Genet. 1981 Aug;20(2):152-60. doi: 10.1111/j.1399-0004.1981.tb01821.x.

The natural history of the severe form of Hunter's syndrome: a study based on 52 cases.重型亨特综合征的自然病史：一项基于52例病例的研究。

Dev Med Child Neurol. 1983 Aug;25(4):481-9. doi: 10.1111/j.1469-8749.1983.tb13794.x.

[Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses].[溶酶体粘多糖分解代谢遗传缺陷引起的疾病。粘多糖贮积症]

Dtsch Med Wochenschr. 1974 Jan 25;99(4):144 passim. doi: 10.1055/s-0028-1107727.

The systemic mucopolysaccharidoses.全身性黏多糖贮积症

Ergeb Inn Med Kinderheilkd. 1972;32:165-265. doi: 10.1007/978-3-642-65300-1_4.

Sanfilippo type C syndrome in two sisters.两姐妹患C型Sanfilippo综合征。

Acta Paediatr Scand. 1985 Jan;74(1):137-9. doi: 10.1111/j.1651-2227.1985.tb10936.x.

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