Odee: Clyde Lopez
OfbọChị Okike: 19 Julai 2021
DatebọChị Mmelite: 23 Jenuari 2025
Anonim
Mucopolysaccharide Storage Disease Type I: Hurler, Hurler-Scheie, and Scheie syndromes
Vidio: Mucopolysaccharide Storage Disease Type I: Hurler, Hurler-Scheie, and Scheie syndromes

Mucopolysaccharides bụ agbụ ogologo nke mkpụrụ ndụ shuga nke a na-ahụ n'ime ahụ dum, na-abụkarị imi na mmiri gburugburu nkwonkwo. A na-akpọkarị ha glycosaminoglycans.

Mgbe aru enweghi ike imebi mucopolysaccharides, onodu a na akpo mucopolysaccharidoses (MPS). MPS na-ezo aka na otu nsogbu ọrịa nke ketara eketa nke metabolism. Ndị nwere MPS enweghị nke ọ bụla, ma ọ bụ zuru oke, nke ihe (enzyme) chọrọ iji mebie ụdọ akuku shuga.

Dị MPS gụnyere:

  • MPS I (Ọrịa Hurler; Ọrịa Hurler-Scheie; Ọrịa Scheie)
  • MPS II (Ọrịa Hunter)
  • MPS III (ọrịa Sanfilippo)
  • MPS IV (ọrịa Morquio)

Glycosaminoglycans; AKAG

Kumar V, Abbas AK, Aster JC. Nsogbu mkpụrụ ndụ ihe nketa. Na: Kumar V, Abbas AK, Aster JC, eds. Robbins na Cotran Pathologic Basis nke Ọrịa. Agba nke 9. Philadelphia, PA: Elsevier Saunders; 2015: isi 5.

Pyeritz RE. Ọrịa ketara eketa nke anụ ahụ jikọtara ọnụ. Na: Goldman L, Schafer AI, eds. Ọgwụ Goldman-Cecil. Nke 26th. Philadelphia, PA: Elsevier; 2020: isi 244.


Ugwueke JW. Mucopolysaccharidoses. Na: Kliegman RM, St. Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, eds. Nelson Akwụkwọ ọgụgụ nke Ọrịa edimụaka. 21nke. Philadelphia, PA: Elsevier; 2020: isi 107.

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