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Xu, R. Mucopolysaccharidosis Type VII. Encyclopedia. Available online: https://encyclopedia.pub/entry/4326 (accessed on 29 September 2026).
Xu R. Mucopolysaccharidosis Type VII. Encyclopedia. Available at: https://encyclopedia.pub/entry/4326. Accessed September 29, 2026.
Xu, Rita. "Mucopolysaccharidosis Type VII" Encyclopedia, https://encyclopedia.pub/entry/4326 (accessed September 29, 2026).
Xu, R. (2020, December 23). Mucopolysaccharidosis Type VII. In Encyclopedia. https://encyclopedia.pub/entry/4326
Xu, Rita. "Mucopolysaccharidosis Type VII." Encyclopedia. Web. 23 December, 2020.
Mucopolysaccharidosis Type VII
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/mucopolysaccharidosis-type-vii

Mucopolysaccharidosis type VII (MPS VII), also known as Sly syndrome, is a progressive condition that affects most tissues and organs. The severity of MPS VII varies widely among affected individuals.

genetic conditions

References

  1. Metcalf JA, Zhang Y, Hilton MJ, Long F, Ponder KP. Mechanism of shortenedbones in mucopolysaccharidosis VII. Mol Genet Metab. 2009 Jul;97(3):202-11. doi: 10.1016/j.ymgme.2009.03.005.
  2. Muenzer J. The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations. J Pediatr. 2004 May;144(5 Suppl):S27-34.Review.
  3. Tomatsu S, Montaño AM, Dung VC, Grubb JH, Sly WS. Mutations and polymorphisms in GUSB gene in mucopolysaccharidosis VII (Sly Syndrome). Hum Mutat. 2009Apr;30(4):511-9. doi: 10.1002/humu.20828. Review.
  4. Venkat-Raman N, Sebire NJ, Murphy KW. Recurrent fetal hydrops due tomucopolysaccharidoses type VII. Fetal Diagn Ther. 2006;21(3):250-4. Review.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Rita Xu
View Times: 611
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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