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iduronate sulfatase in skin
reduced results from
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what is 'iduronate sulfatase in skin'?
Definition for iduronate sulfatase in skin
iduronate sulfatase in skin is a medical procedure used for such diagnoses as: Hunter Syndrome.
related diagnosis for 'iduronate sulfatase in skin'
1 - 1 of
1
diagnosis
Hunter Syndrome
abnormal accumulation of complex carbodyrates in cells; MPS Type 11
iduronate sulfatase in skin and Hunter Syndrome
related procedure for 'iduronate sulfatase in skin'/associated diagnoses
1 - 2 of
2
procedures
X-rays
iduronate sulfatase in skin and X-rays
urine heparan sulfate
iduronate sulfatase in skin and urine heparan sulfate
related medication for 'iduronate sulfatase in skin'/associated diagnoses
1 - 2 of
2
drugs
idursulfase (elaprase)
iduronate sulfatase in skin and idursulfase (elaprase)
The following are types of physicians relevant for 'iduronate sulfatase in skin'.
related types of physicians 'family practitioner, genetics specialist, internist, metabolic specialist'
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web search results for 'iduronate sulfatase in skin'?
Results
1 - 50
- iduronate sulfatase in skin
eMedicine - Mucopolysaccharidosis Type II : Article by Nancy Braverman
In MPS II, because of the lack of iduronate sulfatase (IDS), dermatan and ... The skin lesions, which develop in a reticular pattern and appear pebbly, are ...
http://www.emedicine.com/ped/topic1029.htm
www.emedicine.com
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summary
MedlinePlus Medical Encyclopedia: Hunter syndrome
Decreased iduronate sulfatase enzyme activity in serum or cells ... iduronate sulfatase (may be studied in serum, white blood cells, skin cells) ...
http://www.nlm.nih.gov/medlineplus/ency/article/001203.htm
www.nlm.nih.gov
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summary
Hunter syndrome - Wikipedia, the free encyclopedia
... the body due to a deficiency or absence of the enzyme iduronate-2-sulfatase ... In addition, pebbly, ivory-colored skin lesions may be found on the upper arms ...
http://en.wikipedia.org/wiki/Hunter_syndrome
en.wikipedia.org
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summary
Iduronate 2-sulfatase, Homo sapiens - UniGene Hs.460960
A summary of the mRNA sequence representatives for a transcribed locus ... uterus; pharynx; esophagus; spleen; skin; mammary gland; thymus; vascular; liver; ...
http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&MAXEST=999999&CID=460960
www.ncbi.nlm.nih.gov
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summary
The correction of hunter fibroblasts by exogenous iduronate sulfate ...
The exogenous addition of iduronate sulfate sulfatase to cultured fibroblasts of ... Mucopolysaccharide accumulation in cultured skin fibroblasts derived from ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1685092
www.pubmedcentral.nih.gov
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summary
TKT reports results of I2S trial for Hunter syndrome - Rare/Orphan ...
... trial evaluating its drug iduronate-2-sulfatase (I2S) in the treatment of Hunter syndrome... the protein desmoglein in skin and mucous membrane cells. ...
http://rarediseases.about.com/b/a/2005_06.htm
rarediseases.about.com
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summary
GeMCRIS - Gene Transfer Protocol Reports
... Mediated Transfer of the Iduronate-2-Sulfatase Gene into Lymphocytes for ... Pain in extremity. Peripheral vascular disorder. Skin ulcer ...
http://www.gemcris.od.nih.gov/Contents/GC_CT_RPT.asp?offset=80
www.gemcris.od.nih.gov
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summary
eMedicine - Mucopolysaccharidoses Types I-VII : Article by Janette ...
... 6-sulfatase on fibroblast culture obtained from a skin biopsy sample. ... type II by measurement of iduronate-2-sulfatase in dried blood spots and plasma samples. ...
http://emedicine.com/derm/topic710.htm
emedicine.com
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Mucopolysaccharidoses Fact Sheet: National Institute of Neurological ...
MPS II, Hunter syndrome, is caused by lack of the enzyme iduronate sulfatase. ... Thickened skin and mild changes in facial features, bone, and skeletal ...
http://www.ninds.nih.gov/disorders/mucopolysaccharidoses/det...
www.ninds.nih.gov
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summary
Mucopolysaccharidosis - Wikipedia, the free encyclopedia
... iduronate sulfatase deficiency, is caused by lack of the enzyme iduronate sulfatase. ... Thickened skin and mild changes in facial features, bone, and skeletal ...
http://en.wikipedia.org/wiki/Mucopolysaccharidosis
en.wikipedia.org
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summary
eMedicine - Mucopolysaccharidosis Type II : Article Excerpt by Nancy ...
Dermatan sulfate is found mostly in skin but is also found in blood vessels, the ... In MPS II, because of the lack of iduronate sulfatase (IDS), dermatan and ...
http://www.emedicine.com/ped/byname/mucopolysaccharidosis-type-ii.htm
www.emedicine.com
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summary
Iduronate 2-sulfatase, Mus musculus - UniGene Mm.233083
A summary of the mRNA sequence representatives for a transcribed locus ... intestine; liver; spleen; eye; heart; extraembryonic tissue; skin; pineal gland ...
http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=233083
www.ncbi.nlm.nih.gov
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summary
X-linked Hunter syndrome: the heterozygous phenotype in cell culture.
... skin of three Hunter heterozygotes have been examined for iduronate sulfatase ... Liebaers I, Neufeld E. Iduronate sulfatase activity in serum, lymphocytes, and ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1685417
www.pubmedcentral.nih.gov
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summary
Hunter Syndrome
ivory-colored skin lesions on the upper back and sides of the upper ... Iduronate-2-sulfatase Enzyme Replacement Therapy in Mucopolysaccharidosis II (MPS II) ...
http://rarediseases.about.com/cs/huntersyndrome/a/022204.htm
rarediseases.about.com
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summary
MedlinePlus Medical Encyclopedia: Topics beginning with Mg-Mz
Mottling see Skin color - patchy. Mountain fever see Colorado tick fever ... Mucopolysaccharidosis type II, Iduronate sulfatase deficiency see Hunter syndrome ...
http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_Mg-Mz.htm
www.nlm.nih.gov
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summary
Presence of arylsulfatase A (ARS A) in multiple sulfatase deficiency ...
Multiple sulfatase deficiencies in cultured skin fibroblasts. ... Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndrome. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1685586
www.pubmedcentral.nih.gov
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eMedicine - Connective Tissue Nevus : Article by Steven Brett Sloan
In Buschke-Ollendorf syndrome, the skin changes may be delayed until adulthood. ... syndrome is the lack of iduronate sulfatase, leading to the accumulation of the ...
http://emedicine.com/derm/topic83.htm
emedicine.com
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summary
Mucopolysaccharidosis - Wikipedia, the free encyclopedia
... iduronate sulfatase deficiency, is caused by lack of the enzyme iduronate sulfatase. ... Thickened skin and mild changes in facial features, bone, and skeletal ...
http://en.wikipedia.org/wiki/MPS_I
en.wikipedia.org
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summary
eMedicine - Lysosomal Storage Disease : Article by Noah S Scheinfeld
... increase in serum beta-hexosaminidase, iduronate sulfatase, and arylsulfatase A is diagnostic. ... findings in type II include dry skin that is ...
http://www.emedicine.com/neuro/topic668.htm
www.emedicine.com
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Chromosome X open reading frame 40A, Homo sapiens - UniGene Hs.654738
iduronate 2-sulfatase isoform b. M. musculus. 90.3. 62. GENE EXPRESSION ... intestine; muscle; uterus; parathyroid; skin; adrenal gland; spleen; bladder; ...
http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=654738
www.ncbi.nlm.nih.gov
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summary
APPENDIX D
As noted in the subsections of Section IV-C-1-b-(1), the Director, NIH, may take ... syringae, and Erwinia herbicola carrying in vitro generated deletions of all or ...
http://www4.od.nih.gov/oba/RAC/guidelines_02/APPENDIX_D.htm
www4.od.nih.gov
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summary
National Inventory of Clinical Laboratory Testing Services (NICLTS ...
Anti-Skin Abs. Anti-Cardiolipin Abs. Anti-Parietal Cell Abs. Anti ... Iduronate Sulfatase. Uroporphyrinogen Decarboxylase. Sphingomyelinase. Pyruvate kinase ...
http://wwwn.cdc.gov/mlp/nicltsal.aspx
wwwn.cdc.gov
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summary
Genetic complementation studies of multiple sulfatase deficiency.
... showed a significant increase in iduronate-sulfate-sulfatase activity. ... Multiple sulfatase deficiencies in cultured skin fibroblasts. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=411892
www.pubmedcentral.nih.gov
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Rare Diseases Blog with Mary Kugler, R.N. June 2005 Archive
... trial evaluating its drug iduronate-2-sulfatase (I2S) in the treatment of ... autoantibodies attack the protein desmoglein in skin and mucous membrane cells. ...
http://rarediseases.about.com/b/a/200506.htm?p=1
rarediseases.about.com
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summary
eMedicine - Mucopolysaccharidosis : Article by Tarek Bittar
... MPS is characterized by pebbly ivory skin lesions on the back, arms, and ... levels of the lysosomal enzyme iduronate-2-sulfatase in MPS II.14, 12, 10, 8 ...
http://www.emedicine.com/orthoped/topic203.htm
www.emedicine.com
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summary
Co-cluster Matrix
IDS Iduronate 2-sulfatase (Hunter syndrome) Chr.X [470009, (IW), 5':AA029212, 3':AA029213] ... acid-binding protein [human, skin, mRNA, 735 nt] [5':W95692, ...
http://discover.nci.nih.gov/external/CIM_example3/cgi_user_matrix.html
discover.nci.nih.gov
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summary
nciarray.nci.nih.gov/gal_files/Hs-FDA-16K-V1.1p10.gal
... 3, alk" 1 1 22 U76248 "SIAH2--seven in absentia homolog 2 (Dr" 1 1 23 Y10805 " ... 1 16 11 AB026289 "NEK6--NIMA (never in mitosis gene a)-r" 1 16 12 AL109939 " ...
http://nciarray.nci.nih.gov/gal_files/Hs-FDA-16K-V1.1p10.gal
nciarray.nci.nih.gov
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National Institute on Aging, David Schlessinger, Ph.D. - Bibliography
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the ... EDA targets revealed by skin gene expression profiles of wild-type, Tabby and ...
http://www.grc.nia.nih.gov/branches/lg/hgu/davidsbio.htm
www.grc.nia.nih.gov
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summary
Genetic Disorders of Glycan Degradation -- Essentials of Glycobiology ...
... bone, joint, and skin problems in mucopolysaccharidose (MPS) I, II, VI, and VII. ... Iduronate-2-sulfatase is followed by ?-iduronidase. ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=glyco2&part=ch41
www.ncbi.nlm.nih.gov
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summary
Sanfilippo syndrome type C: deficiency of acetyl-CoA:alpha ...
... A Syndrome SULFAMIDASE DEFICIENCY IN CULTURED SKIN FIBROBLASTS AND LIVER. ... Liebaers I, Neufeld E. Iduronate sulfatase activity in serum, lymphocytes, and ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=336290
www.pubmedcentral.nih.gov
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summary
Enzyme replacement therapy by fibroblast transplantation: long-term ...
Liebaers I, Neufeld E. Iduronate sulfatase activity in serum, lymphocytes, and ... and appearance of corrective enzyme after skin transplants in Hunter syndrome. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=371928
www.pubmedcentral.nih.gov
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Tartrate resistant acid phosphatase - Wikipedia, the free encyclopedia
... also detectable in the spleen, thymus, liver, kidneys, skin, lung and ... sulfatase - Galactosamine-6 sulfatase - Arylsulfatase A - Iduronate-2-sulfatase ...
http://en.wikipedia.org/wiki/Tartrate_resistant_acid_phosphatase
en.wikipedia.org
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nciarray.nci.nih.gov/gal_files/Hs-HEEBO-v1.0px.gal
1 13 14 "hHC017304" "HIC1--hypermethylated in cancer 1 (HIC1), mRNA. ... 1 17 3 "hHC022380" "RHOF--ras homolog gene family, member F (in filopodia) (RHOF), mRNA. ...
http://nciarray.nci.nih.gov/gal_files/Hs-HEEBO-v1.0px.gal
nciarray.nci.nih.gov
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summary
Hunter syndrome
... iduronate sulfatase (may be studied in serum, white blood cells, skin cells) Genetic testing may show mutation in the iduronate sulfatase gene. Treatment ...
http://adam.about.com/encyclopedia/infectiousdiseases/Hunter...
adam.about.com
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SNPs Localized to Chromosome X Interval 15
Iduronate 2-sulfatase (Hunter syndrome) CGAP-C-64304. CGAP-C-247597 ... Iduronate 2-sulfatase (Hunter syndrome) CGAP-C-2428642. CGAP-C-2428643. CGAP-C-2428649 ...
http://gai.nci.nih.gov/cgi-bin/ival.cgi?c=23&i=15
gai.nci.nih.gov
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summary
eMedicine - I-Cell Disease (Mucolipidosis Type II) : Article by Karl S Roth
... activities of beta-hexosaminidase, iduronate sulfatase, and arylsulfatase A are ... of storage materials in cultured skin fibroblasts from patients with ...
http://www.emedicine.com/ped/topic1150.htm
www.emedicine.com
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Arylsulfatase A Deficiency -- GeneReviews -- NCBI Bookshelf
( 2) Cultured skin fibroblasts have often been used to confirm deficiency of ARSA ... arylsulfatase C, iduronate sulfatase deficiency [the enzyme that is deficient in ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&partid=1130
www.ncbi.nlm.nih.gov
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summary
ATF 1 35 5 TypeGenePix arrayList V1.0 BlockCount32 BlockType 0 ...
can in acute undifferentiated leukemia" 1 6 5 "IMAGE:781019" "PON2--Paraoxonase ... "NEK3--NIMA (never in mitosis gene a)-related kinase 3=nek3 protein kinase" 2 9 ...
http://nciarray.nci.nih.gov/gal_files/Hs-ROSP-NTU8k-v1px.gal
nciarray.nci.nih.gov
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summary
www.nlm.nih.gov/mesh/2K/indman/chapter_28.html
Suggestions and restrictions on individual terms appear in the ANNOTATED MeSH. ... Radiation injury to the skin caused by radiotherapy. ...
http://www.nlm.nih.gov/mesh/2K/indman/chapter_28.html
www.nlm.nih.gov
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summary
Human glucosamine-6-sulphatase deficiency. Diagnostic enzymology ...
Residual 6S activity present in the skin fibroblast homogenates from MPS IIID ... A sulfatase specific for glucuronic acid 2-sulfate residues in glycosaminoglycans. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1130825
www.pubmedcentral.nih.gov
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summary
discover.nci.nih.gov/nature2000/data/selected_data/t_matrix.xls
[5':H23354, 3':H23243] \IDS Iduronate 2-sulfatase (Hunter syndrome) Chr.X [470009, ... retinoic acid-binding protein [human, skin, mRNA, 735 nt] [5':W95692, 3' ...
http://discover.nci.nih.gov/nature2000/data/selected_data/t_matrix.xls
discover.nci.nih.gov
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summary
Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/6 ...
Hard skin syndrome Parana type. Harding ataxia. Harrod ... Iduronate 2-sulfatase deficiency. IFAP syndrome. IGDA syndrome. Ilyina Amoashy Grygory syndrome ...
http://en.wikipedia.org/wiki/Wikipedia:WikiProject_Missing_e...
en.wikipedia.org
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Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and ...
These skin eruptions, first noted in Hunter's original presentation, are said to ... a regional duplication distal to the human iduronate-2-sulfate sulfatase locus. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2234442
www.pubmedcentral.nih.gov
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summary
nciarray.nci.nih.gov/gal_files/Hsfa.gal
1 13 9 "hHC017304" "HIC1--hypermethylated in cancer 1 (HIC1), mRNA. ... 1 16 28 "hHC022380" "RHOF--ras homolog gene family, member F (in filopodia) (RHOF), mRNA. ...
http://nciarray.nci.nih.gov/gal_files/Hsfa.gal
nciarray.nci.nih.gov
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summary
cDNA Library 20865 [Homo sapiens]
Human epidermis granular keratinocytes ... Skin. Tissue: Epidermis. Cell type: Keratinocyte ... Iduronate 2-sulfatase. 1. 617. Hs.460693 ...
http://www.ncbi.nlm.nih.gov/UniGene/library.cgi?LID=20865&PAGE=6
www.ncbi.nlm.nih.gov
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summary
nciarray.nci.nih.gov/gal_files/Mm-FDA-16K-V2.0p3.gal
... 6 days neonate skin cDNA, RIKEN full-length enriched library, clone:A030005L19 ... 2 4 10 "M200002423" "Siah1a--seven in absentia 1A (Siah1a), mRNA. ...
http://nciarray.nci.nih.gov/gal_files/Mm-FDA-16K-V2.0p3.gal
nciarray.nci.nih.gov
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summary
Hunter Syndrome
... of an enzyme known as iduronate sulfatase, which is needed to break down ... See Baby Skin Problems. Test Your Health IQ. And you could win a Wii Fit from WebMD. ...
http://children.webmd.com/hunter-syndrome
children.webmd.com
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summary
Arylsulfatase A Deficiency
( 2) Cultured skin ... B, arylsulfatase C, iduronate sulfatase [(deficient in Hunter syndrome ... enzyme (deficient in multiple sulfatase deficiency) is. Page ...
http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...
www.ncbi.nlm.nih.gov
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summary
Human alpha-L-iduronidase. Catalytic properties and an integrated role ...
Human liver iduronate-2-sulphatase. Purification, characterization and ... Glucuronate-2-sulphatase activity in cultured human skin fibroblast homogenates. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1130872
www.pubmedcentral.nih.gov
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summary
Glucuronate-2-sulphatase activity in cultured human skin fibroblast ...
A sulfatase specific for glucuronic acid 2-sulfate residues in glycosaminoglycans. ... Human liver iduronate-2-sulphatase. Purification, characterization and ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1151618
www.pubmedcentral.nih.gov
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summary
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