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41. Sacbee.com -- Sanfilippo Syndrome
sanfilippo syndrome, 24hour local, state, national and world news, plus politics, sports, business, lifestyle and entertainment coverage, columnists, humor
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Facing the future together
The Bennett family struggles to cope as all three children have a rare, deadly disease
By Cynthia Hubert Bee Staff Writer
Ciara, Hunter and Tommy Bennett are outdoors on a brilliant spring afternoon in Amador County, their naps finished, their little tennis shoes tromping in a vast, green yard. The youngsters suffer from a genetic disorder known as Sanfilippo syndrome, which is caused by the body's inability to produce certain enzymes and strikes about 1 in 70,000 babies. The absence of the enzymes causes sugar molecules called mucopolysaccharides to build up in the body, causing progressive damage to the heart, bones, joints, and respiratory and central nervous systems. Sanfilippo youngsters, who inherit defective genes from both parents, generally die before the age of 13.

42. Sanfilippo Syndrome Genetic Disorders Conditions And Diseases Health
sanfilippo syndrome (MPS III) ? an autosomal recessive hereditary disorder ? is characterized by severe mental deterioration ? mild physical defects and
http://www.interactiva.org/Dir/I/English/Health/Conditions_and_Diseases/Genetic_
www.interactiva.org English Deutsch Espa±ol ... Sanfilippo Syndrome Sanfilippo Syndrome English Health Conditions and Diseases Musculoskeletal Disorders: Connective Tissue
English Health Conditions and Diseases: Nutrition and Metabolism Disorders
English Health Conditions and Diseases: Rare Disorders
MPS III: Sanfilippo Syndrome

www.mpssociety.org/mps3.html

Conditions and Diseases Genetic Disorders Sanfilippo Syndrome.
Information ( MPS III: Sanfilippo Syndrome ) including the causes, different forms, the inheritance and how the disorder progresses.
Bennett Children's Foundation

www.helpachild.net

Conditions and Diseases Genetic Disorders Sanfilippo Syndrome.
Founded by parents of three young children who suffer from Sanfilippo Syndrome ( Bennett Children's Foundation ) a degenerative genetic disorder that is usually fatal before the teens. Raising awareness of the condition and enlisting financial support. NORD: Sanfilippo Syndrome www.rarediseases.org/search/rdbdetail_abstract.html?disname=Sanfilippo%20Syndrome Conditions and Diseases Genetic Disorders Sanfilippo Syndrome. Offers a list of synonyms ( NORD: Sanfilippo Syndrome ) a general discussion and further resources.

43. KXTV News10 TV -- Tommy Bennett Loses Battle With Sanfilippo Syndrome
h elpachild . net. Tommy Bennett Loses Battle with sanfilippo syndrome. Tommy Bennett, the fouryear-old boy from Ione who has been
http://www.helpachild.net/bennett/publicity/tv/kxtv/11-26-03.htm
h e l p a c h i l d . n e t
Tommy Bennett Loses Battle with Sanfilippo Syndrome Tommy Bennett, the four-year-old boy from Ione who has been battling a metabolic disorder, died early Tuesday morning at Duke University Children's Center. Just a month ago, Tommy underwent a third stem cell transplant in an effort to fight Sanfilippo syndrome, a rare and almost invariably fatal genetic disorder in which the body lacks a key enzyme needed to break down sugar. As the incompletely metabolized sugar builds up in organ systems, the body begins to break down. Death usually results before age 20. Tommy Bennett was considered a good candidate for an experimental procedure, in which stems cells from umbilical cord blood are transplanted into the body of a Sanfilippo syndrome patient. Because stem cells have the unique ability to grow into virtually any other form of cells, they can transform in the cells that produce the missing enzyme. The results of the procedure were initially promising. Tommy Bennett's body began producing the enzyme-producing cells. However, earlier this month the boy's body began rejecting the transplanted cells. His lungs, liver and kidneys began to fail. He fell into a coma as his condition gradually deteriorated.

44. ABC11 TV -- Sanfilippo Syndrome
net. Monday, November 04, 2002. sanfilippo syndrome. But a new procedure may give one boy a chance at life. The three children were born with sanfilippo syndrome.
http://www.helpachild.net/bennett/publicity/tv/abc11tv/11-4-02.htm
h e l p a c h i l d . n e t
Monday, November 04, 2002 Sanfilippo Syndrome By Angela Hampton
A California family has come to Duke for an experimental treatment they hope will save one of their children's lives. All three of their kids have a rare genetic disease that will probably kill them by age 15. But a new procedure may give one boy a chance at life. The three children were born with Sanfilippo Syndrome. It's a rare disease that develops in the first few years of a child's life, and is often mis-diagnosed. There is no cure. The children's parents have brought them to Duke because it's the only medical center in the world doing stem cell transplants using umbilical cord blood to try to reverse some of the symptoms of Sanfilippo. John Bennett has brought his sons from northern California to Durham, to try to save their young lives. "Feed the fishies. Fishies like bread too." Three-year-old Tommy, and 4-year-old Hunter, are very sick with a rare genetic disease. Sanfilippo Syndrome robs their little bodies of an enzyme that breaks down sugar molecules. It causes severe brain and organ damage, and premature death. "Most Sanfilippo kids, if they do live to 15, are bedridden vegetables."

45. Sanfilippo Syndrome Type A
Current Page sanfilippo syndrome Type A. The UK s largest coursework and essay database, All Categories This Category. sanfilippo syndrome Type A.
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Below is a short sample of the essay "Sanfilippo Syndrome Type A" . If you sign up you could be reading the rest of this essay in under two minutes. Registered users should log in to view the full essay ... rom the ear to the brain that is reported to be about three second delay. He has slight hip dyplasia, which is progressively getting worse due to degenerativeness of disorder. PHYSICAL EXAM/OBSERVATION: He is currently walking inward and on his toes, which I have seen him, trip over his own two feet in the course of this visit. . He is wearing customized kneepads to stop injuries to his knees due to falling, ... All formatting has been removed from the sample of this essay. Inside Coursework.Info , all coursework and essays can be viewed with all of the original formatting retained - including pictures, tables, images and graphs, as well as the . You may also be interested in the word count, writing time and other details

46. EMedicine - Mucopolysaccharidosis Type III : Article By Donald Nash, PhD†
Synonyms and related keywords MPS, MPSIII, sanfilippo syndrome, Sanfilippo’s syndrome, MPS type IIIA, Sanfilippo A, MPS type IIIB, Sanfilippo B, MPS type
http://www.emedicine.com/ped/topic2040.htm
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Mucopolysaccharidosis Type III
Last Updated: June 19, 2003 Rate this Article Email to a Colleague Synonyms and related keywords: MPS, MPS-III, Sanfilippo syndrome, Sanfilippo’s syndrome, MPS type IIIA, Sanfilippo A, MPS type IIIB, Sanfilippo B, MPS type IIIC, Sanfilippo C, MPS type IIID, Sanfilippo D AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography
Author: Donald Nash, PhD† , Former Professor, Department of Biology, Colorado State University Coauthor(s): Surendra Varma, MD , Vice-Chairman and Program Director, University Distinguished Professor, Department of Pediatrics, Texas Tech University School of Medicine Donald Nash, PhD†, is a member of the following medical societies: American Association for Advancement of Science American Society of Human Genetics American Society of Mammalogists Behavior Genetics Association ... Sigma Xi , and Teratology Society Editor(s): Karl S Roth, MD

47. EMedicine - Mucopolysaccharidoses Types I-VII : Article Excerpt By: Janette Balo
MPS type IS, Scheie syndrome, MPS type V, MPS type IH/S, HurlerScheie syndrome, MPS type II, Hunter syndrome, MPS type III-A, sanfilippo syndrome type A, MPS
http://www.emedicine.com/derm/byname/mucopolysaccharidoses-types-i-vii.htm
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Excerpt from Mucopolysaccharidoses Types I-VII
Synonyms, Key Words, and Related Terms: MPS, lysosomal storage disease, glycosaminoglycans, GAGs, MPS type I-H, Hurler syndrome, MPS type I-S, Scheie syndrome, MPS type V, MPS type I-H/S, Hurler-Scheie syndrome, MPS type II, Hunter syndrome, MPS type III-A, Sanfilippo syndrome type A, MPS III-B, Sanfilippo syndrome type B, MPS III-C, Sanfilippo syndrome type C, MPS type III-D, Sanfilippo syndrome type D, MPS type IV-A, Morquio syndrome, MPS type IV-B, MPS type VI, Maroteaux-Lamy syndrome, MPS type VII, Sly syndrome
Please click here to view the full topic text: Mucopolysaccharidoses Types I-VII
Background: Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases, each of which is produced by an inherited deficiency of an enzyme involved in the degradation of acid mucopolysaccharides (now called glycosaminoglycans [GAGs]). These diseases are autosomal recessive, except for MPS type II, which is X-linked. Pathophysiology: GAGs are long, linear polysaccharide molecules composed of repeating dimers, each of which contains a hexuronic acid (or galactose in the case of keratan sulfate) and an amino sugar. The large proteoglycan molecules made up of protein cores and GAG branches are secreted by cells and constitute a significant fraction of the extracellular matrix of the connective tissue. The turnover of these molecules depends on their subsequent internalization by endocytosis, their delivery to the lysosomes, and their digestion by lysosomal enzymes. The enzyme deficiencies lead to the accumulation of mucopolysaccharides in the lysosomes of the cells in the connective tissue and to an increase in their excretion in the urine. The types of MPSs linked to specific enzyme deficiencies are listed below; some have been assigned an Enzyme Commission (EC) number.

48. Health Library -
sanfilippo syndrome. Important It is possible that the main title of the report sanfilippo syndrome is not the name you expected.
http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw

49. ► Sanfilippo Syndrome
sanfilippo syndrome. This substance is called heparan sulfate, and in sanfilippo syndrome, large amounts of it are excreted in the urine. Alternative Names
http://www.kernanhospital.com/ency/article/001210.htm
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Sanfilippo syndrome
Overview Symptoms Treatment Prevention Definition: Sanfilippo syndrome is one of the hereditary mucopolysaccharide storage diseases, and it is characterized by the absence of one of several enzymes . These enzymes help the body get rid of a substance normally found outside of our cells called a mucopolysaccharide. This substance is called heparan sulfate, and in Sanfilippo syndrome, large amounts of it are excreted in the urine.
Alternative Names: Mucopolysaccharidosis type III (subtypes A - B - C-D); Type IIIA = heparan sulfate sulfatase deficiency; Type IIIB = N-acetylglucosaminidase deficiency; Type IIID = N-acetylglucosamine-6-sulfate sulfatase deficiency
Causes, incidence, and risk factors: Sanfilippo syndrome is transmitted as an autosomal recessive trait. It is possibly the most common of the mucopolysaccharide storage diseases. Sanfilippo syndrome has a relatively late onset rather than during the first year of life. It shares, in common with most of the mucopolysaccharide storage diseases, coarse facial features, decreased mental development that progresses to severe

50. HealthCentral - Pediatrics Encyclopedia - Sanfilippo Syndrome
Pediatric Health Encyclopedia, sanfilippo syndrome. Causes, incidence, and risk factors sanfilippo syndrome is transmitted as an autosomal recessive trait.
http://www.healthcentral.com/peds/top/001210.cfm
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51. Health - Conditions And Diseases - Genetic Disorders - Sanfilippo
Top Health Conditions and Diseases Genetic Disorders sanfilippo syndrome See also Health Conditions and Diseases Musculoskeletal
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52. Sanfilippo Syndrome - MiMi
Home, sanfilippo syndrome. sanfilippo syndrome is transmitted as an trait. It is possibly the most common of the mucopolysaccharide storage diseases.
http://en.mimi.hu/disease/sanfilippo_syndrome.html
Home Menu(0); MimiF3("Disease",0); pozicio('Disease','Sanfilippo syndrome') MimiF1("Disease",0); Sanfilippo syndrome
CreateTd(0) Sanfilippo syndrome
Definition:
Sanfilippo syndrome is one of the hereditary mucopolysaccharide storage diseases, and it is characterized by the absence of one of several . These enzyme s help the body get rid of a substance normally found outside of our cells called a mucopolysaccharide. callurl('http://www.umm.edu/ency/article/001210.htm'); CreateTd(1) Sanfilippo syndrome is transmitted as an trait. It is possibly the most common of the mucopolysaccharide storage diseases. In Sanfilippo syndrome , onset is relatively late, rather than during the first year of life.
As with most of the mucopolysaccharide storage diseases, callurl('http://www.nlm.nih.gov/medlineplus/ency/article/001210.htm'); CreateTd(2) Like Sanfilippo syndrome , onset of symptoms is delayed until after the first year, and life expectancy may exceed 20 years. Unlike Sanfilippo syndrome , the mental development is often normal.
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53. SANFILIPPO SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE III)
Features Listed For sanfilippo syndrome (MUCOPOLYSACCHARIDOSIS TYPE III). McKusick Acetabulum, general abnormalities; Advanced bone
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?1512

54. SGSH
CM002392, 32, GACGGC, Asp-Gly, sanfilippo syndrome A, 1. CM981795, 40, gTAC-AAC, Tyr-Asn, sanfilippo syndrome A, 2. CM021148, 42, AACa-AAA, Asn-Lys, sanfilippo syndrome A, 3.
http://archive.uwcm.ac.uk/uwcm/mg/ns/1/1319101.html
SGSH
Nucleotide substitutions (missense / nonsense)
Accession
Number Codon Nucleotide Amino acid Phenotype Reference
GAC-GGC Asp-Gly Sanfilippo syndrome A gTAC-AAC Tyr-Asn Sanfilippo syndrome A AACa-AAA Asn-Lys Sanfilippo syndrome A cGCC-ACC Ala-Thr Sanfilippo syndrome A TCG-TGG Ser-Trp Sanfilippo syndrome A cCGC-TGC Arg-Cys Sanfilippo syndrome A CGC-CAC Arg-His Sanfilippo syndrome A cACT-CCT Thr-Pro Sanfilippo syndrome A gCAT-TAT His-Tyr Sanfilippo syndrome A CAG-CGG Gln-Arg Sanfilippo syndrome A cGGG-AGG Gly-Arg Sanfilippo syndrome A cGGG-AGG Gly-Arg Sanfilippo syndrome A CCG-CTG Pro-Leu Sanfilippo syndrome A cGTG-ATG Val-Met Sanfilippo syndrome A ACG-ATG Thr-Met Sanfilippo syndrome A CTC-CCC Leu-Pro Sanfilippo syndrome A CGG-CAG Arg-Gln Sanfilippo syndrome A gCGG-TGG Arg-Trp Sanfilippo syndrome A cGAC-AAC Asp-Asn Sanfilippo syndrome A cCGC-TGC Arg-Cys Sanfilippo syndrome A TTCt-TTG Phe-Leu Sanfilippo syndrome A CGT-CCT Arg-Pro Sanfilippo syndrome A TGG-TAG Trp-Term Sanfilippo syndrome A CCC-CGC Pro-Arg Sanfilippo syndrome A cCGA-TGA Arg-Term Sanfilippo syndrome A GCC-GGC Ala-Gly Sanfilippo syndrome A cGAC-AAC Asp-Asn Sanfilippo syndrome A GAC-GTC Asp-Val Sanfilippo syndrome A CGC-CAC Arg-His Sanfilippo syndrome A cGAC-AAC Asp-Asn Sanfilippo syndrome A TAC-TCC Tyr-Ser Sanfilippo syndrome A gCCG-TCG Pro-Ser Sanfilippo syndrome A aCCC-TCC Pro-Ser Sanfilippo syndrome A aTCC-CCC Ser-Pro Sanfilippo syndrome A cACC-GCC Thr-Ala Sanfilippo syndrome A ATC-AGC Ile-Ser Sanfilippo syndrome A gGCC-CCC

55. NAGLU
Translate this page CM990914, 1, cATG-TTG, Met-Leu, sanfilippo syndrome B, 1. CM003004, 35, gCTC-TTC, Leu-Phe, sanfilippo syndrome B, 2. CM981354, 48, TTC-TGC, Phe-Cys, sanfilippo syndrome B, 3.
http://archive.uwcm.ac.uk/uwcm/mg/ns/1/636533.html
NAGLU
Nucleotide substitutions (missense / nonsense)
Accession
Number Codon Nucleotide Amino acid Phenotype Reference
cATG-TTG Met-Leu Sanfilippo syndrome B gCTC-TTC Leu-Phe Sanfilippo syndrome B TTC-TGC Phe-Cys Sanfilippo syndrome B TTCt-TTA Phe-Leu Sanfilippo syndrome B cGGC-AGC Gly-Ser Sanfilippo syndrome B cGGC-TGC Gly-Cys Sanfilippo syndrome B GGC-GAC Gly-Asp Sanfilippo syndrome B cTAC-CAC Tyr-His Sanfilippo syndrome B CAC-CGC His-Arg Sanfilippo syndrome B gCCA-TCA Pro-Ser Sanfilippo syndrome B cCGC-TGC Arg-Cys Sanfilippo syndrome B TAC-TGC Tyr-Cys Sanfilippo syndrome B aGAG-AAG Glu-Lys Sanfilippo syndrome B ATA-AGA Ile-Arg Sanfilippo syndrome B TGGa-TGT Trp-Cys Sanfilippo syndrome B TGG-TAG Trp-Term Sanfilippo syndrome B gCGA-TGA Arg-Term Sanfilippo syndrome B CAC-CCC His-Pro Sanfilippo syndrome B gCGC-TGC Arg-Cys Sanfilippo syndrome B aGTG-ATG Val-Met Sanfilippo syndrome B CCT-CTT Pro-Leu Sanfilippo syndrome B CAT-CGT His-Arg Sanfilippo syndrome B tTGG-CGG Trp-Arg Sanfilippo syndrome B TGC-TTC Cys-Phe Sanfilippo syndrome B CTT-CCT Leu-Pro Sanfilippo syndrome B cGGG-AGG Gly-Arg Sanfilippo syndrome B gCGA-TGA Arg-Term Sanfilippo syndrome B TAT-TGT Tyr-Cys Sanfilippo syndrome B tTTC-CTC Phe-Leu Sanfilippo syndrome B cGTC-TTC Val-Phe Sanfilippo syndrome B tGAG-TAG Glu-Term Sanfilippo syndrome B CCG-CTG Pro-Leu Sanfilippo syndrome B TGG-TAG Trp-Term Sanfilippo syndrome B TTT-TCT Phe-Ser Sanfilippo syndrome B GGA-GAA Gly-Glu Sanfilippo syndrome B CAT-CGT His-Arg Sanfilippo syndrome B

56. Qango : Health: Diseases And Conditions: S: Sanfilippo Syndrome
category Options Help. Home Health Diseases and Conditions S sanfilippo syndrome, Suggest a Site. Health, etc. If you would
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57. Netscape Search: Top > Health > Conditions And Diseases > Genetic Disorders > Sa
new physicians. http//www.HealthGrades.com. Sites in sanfilippo syndrome About these results. •. Ben s Dream. Information about
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58. Conditions And Diseases: Genetic Disorders: Sanfilippo Syndrome| Treasure Coast
Information on Conditions and Diseases, Genetic Disorders, sanfilippo syndrome and much more Treasure Coast Health. Treasure Coast
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59. Fablis Directory For /Health/Conditions_and_Diseases/Genetic_Disorders/Sanfilipp
sanfilippo syndrome. MPS III sanfilippo syndrome Information, including the causes, different forms, the inheritance and how the disorder progresses.
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60. WebGuest Directory - Health : Conditions And Diseases : Genetic Disorders : Sanf
Dream Information about a foundation dedicated to increasing awareness of sanfilippo syndrome and raising funds to support research aimed at finding a cure.
http://directory.webguest.com/Health/Conditions_and_Diseases/Genetic_Disorders/S
Health Conditions and Diseases Genetic Disorders : Sanfilippo Syndrome
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Sites:
  • Ben's Dream - Information about a foundation dedicated to increasing awareness of Sanfilippo Syndrome and raising funds to support research aimed at finding a cure. Includes a newsletter. Bennett Children's Foundation - Founded by parents of three young children who suffer from Sanfilippo Syndrome, a degenerative genetic disorder that is usually fatal before the teens. Raising awareness of the condition and enlisting financial support. Children's Medical Research Foundation - A non-profit foundation formed to raise and grant funds for research to find a cure for Sanfilippo Syndrome. MPS III: Sanfilippo Syndrome - Information, including the causes, different forms, the inheritance and how the disorder progresses. NORD: Sanfilippo Syndrome - Offers a list of synonyms, a general discussion and further resources.

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