Sindrom Hunter - Wikipedia Bahasa Melayu, ensiklopedia bebas

Hunter syndrome
Hunter syndrome
Pengelasan dan sumber luaran
ICD-10	E76.1
ICD-9	277.5
OMIM	309900
P. Data Penyakit	6050
MedlinePlus	001203
eMedicine	ped/1029
MeSH	D016532
Penafian perubatan

Sindrom Hunter, atau mucopolysaccharidosis Type II, adalah penyakit penyimpanan lysosomal disebabkan kekurangan (atau ketiadaan) enzim, iduronate-2-sulfatase (I2S).^[1]^[2]^:544 SIndrom ini dinamakan sempena ahli perubatan Charles A. Hunter (1873–1955), yang pertama kali menggambarkannya pada 1917.^[3]^[4] Dilahirkan di Scotland, Hunter berhijrah ke Kanada dan mengamalkan perubatan di Winnipeg, Manitoba.

Lihat juga

Rujukan

^ Wraith JE, Scarpa M, Beck M; dll. (2008). "Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy". Eur. J. Pediatr. 167 (3): 267–77. doi:10.1007/s00431-007-0635-4. PMC 2234442. PMID 18038146. Unknown parameter |month= ignored (bantuan); Explicit use of et al. in: |author= (bantuan)CS1 maint: multiple names: authors list (link)
^ James, William D.; Berger, Timothy G.; dll. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0. Explicit use of et al. in: |author= (bantuan)CS1 maint: multiple names: authors list (link)
^ synd/1109 di Who Named It?
^ C. A. Hunter. A rare disease in two brothers. Proceedings of the Royal Society of Medicine, London, 1917, 10: 104-116.

Pautan luar

MPSsociety.org, National MPS Society
About.com, "Hunter Syndrome", About.com
CCHS-DL.SLIS.ua.edu, Hunter Syndrome Patient/Family Resources CCHS Resources.
Hunterpatients.com
NLM.NIH.gov, GeneReview/NIH/UW entry on Mucopolysaccharidosis Type II
HideandSeek.org, Foundation For Lysosomal Disease Research
Elaprase.com, (idursulfase) website.
ClinicalTrials.gov
LysosomalStorageResearch.ca, The Hunter Disease eClinic and eBook - virtual education (Inggeris), (Jepun)

[pmid18038146-1] Wraith JE, Scarpa M, Beck M; dll. (2008). "Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy". Eur. J. Pediatr. 167 (3): 267–77. doi:10.1007/s00431-007-0635-4. PMC 2234442. PMID 18038146. Unknown parameter |month= ignored (bantuan); Explicit use of et al. in: |author= (bantuan)CS1 maint: multiple names: authors list (link)

[Andrews-2] James, William D.; Berger, Timothy G.; dll. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0. Explicit use of et al. in: |author= (bantuan)CS1 maint: multiple names: authors list (link)

[3] synd/1109 di Who Named It?

[4] C. A. Hunter. A rare disease in two brothers. Proceedings of the Royal Society of Medicine, London, 1917, 10: 104-116.

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Hunter syndrome
Pengelasan dan sumber luaran
ICD-10	E76.1
ICD-9	277.5
OMIM	309900
P. Data Penyakit	6050
MedlinePlus	001203
eMedicine	ped/1029
MeSH	D016532
Penafian perubatan