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         Opitz Syndrome:     more books (17)
  1. Opitz syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Lisa, MS, CGC Andres, 2005
  2. Consider genetic disorder in some milder autism cases.(Child/Adolescent Psychiatry)(Smith-Lemli-Opitz syndrome ): An article from: Clinical Psychiatry News by Linda Little, 2005-08-01
  3. Smith-Lemli-Opitz Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18
  4. Consider SLOS in children presenting with autism.(Behavioral Pediatrics)(Smith-Lemli-Opitz syndrome ): An article from: Pediatric News by Linda Little, 2005-06-01
  5. Smith-Lemli-Opitz Syndrome
  6. Smith-Lemli-Opitz syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Jennifer, MS Wilson, 2005
  7. Opitz: Rett Syndrome by JM OPITZ, 1986-10-01
  8. The Man Behind the Syndrome by Peter Beighton, Greta Beighton, 1991-07-01
  9. Anomalie de La Synthèse Du Cholestérol: Syndrome de Smith-Lemli-Opitz, Nanisme Létal Type Greenberg, Syndrome Child (French Edition)
  10. Consanguineous Marriages in the American Population by George B. Louis Arner, 2010-08-10
  11. Anomalies and Curiosities of Medicine by George M. Gould, 2010-08-02
  12. Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-08-02
  13. Anomalies and Curiosities of Medicine by George M. Gould, 2010-08-02
  14. Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-06-20

41. Conditions And Diseases - Opitz Syndrome Top Links
opitz syndrome Web Site Links. Zach s opitz syndrome Site Offers information, afamily s experience with this syndrome and links to the Opitz Family Network.
http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso
Sub Categories
Related Healthcare Subjects Disabilities Environmental Health Fitness Health Insurance ... Men's Health
Opitz Syndrome Web Site Links Canadian Opitz Family Network A description of Opitz G/BBB Syndrome.
Opitz G/BBB Family Network
Support network for family members whose children have Opitz-G/BBB syndrome.
Zach's Opitz Syndrome Site
Offers information, a family's experience with this syndrome and links to the Opitz Family Network.
NORD - Opitz Syndrome
A look at the alternate names, a general discussion and resources.
National Library of Medicine: OS
Opitz syndrome, the synonyms, a summary and a list of major features.
Other Useful Health Web Links National Institutes of Health (NIH) US Government department in charge of medical research.
AHRQ: Clinical Information
Clinical information on evidence-based practice, clinical guidelines, medical effectiveness, pharmaceutical therapy, new technology, screening and preventive services, outcomes research, and the National Guideline Clearinghouse.
The UK Health Technology Assessment Programme
Site contains details of program's many projects and publications; an NHS national research and development initiative.
U.S. Preventive Services Task Force (USPSTF)

42. Smith-Lemli-Opitz Syndrome - Medical Dictionary Definitions Of Popular Medical T
MedicineNet Home MedTerms medical dictionary AZ List SmithLemli-opitz syndrome. Advanced Search.
http://www.medterms.com/script/main/art.asp?articlekey=21375

43. HONselect - Smith-Lemli-Opitz Syndrome
English SmithLemli-opitz syndrome, - RSH Syndrome - RSH-SLO Syndrome - Smith-Lemli-OpitzSyndrome, Type I - Smith-Lemli-opitz syndrome, Type II - RSH SLO
http://www.hon.ch/HONselect/RareDiseases/C16.131.077.860.html
List of rare diseases: English Deutsch
Language:
MeSH term:
Accepted terms:
English: Smith-Lemli-Opitz Syndrome - RSH Syndrome
- RSH-SLO Syndrome
- Smith-Lemli-Opitz Syndrome, Type I
- Smith-Lemli-Opitz Syndrome, Type II
- RSH SLO Syndrome
- RSH Syndromes
Français: SMITH-LEMLI-OPITZ, SYNDROME - RSH, SYNDROME - SYNDROME RSH - SYNDROME SMITH-LEMLI-OPTIZ Deutsch: Smith-Lemli-Opitz-Syndrom - RSH-Syndrom - SLO-Syndrom Español: SINDROME DE SMITH-LEMLI-OPITZ - SINDROME RSH Português: SINDROME DE SMITH-LEMLI-OPITZ - SINDROME RSH HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: Yes Web sites: English Yes Français Yes Deutsch No Español No Português No Home About us Site map Feedback ... HONewsletter http://www.hon.ch/HONselect/RareDiseases/C16.131.077.860.html Last modified: Wed Apr 28 2004

44. CPS: CPSP Resource Article Smith-Lemli-Opitz Syndrome
SmithLemli-opitz syndrome CPSP resource article published February 2001. Surveillancefor Smith-Lemli-opitz syndrome (SLO) began on January 1, 2000.
http://www.cps.ca/english/CPSP/Resources/RSmithLemliOpitz.htm
Smith-Lemli-Opitz Syndrome CPSP resource article published February 2001 Investigator : Ma gorzata Nowaczyk, MD Surveillance for Smith-Lemli-Opitz syndrome (SLO) began on January 1, 2000. In the first nine months, 27 reports were received of which 10 have been confirmed. The CPSP has been successful in identifying both newly diagnosed patients as well as patients with previous clinical diagnosis of SLO who received biochemical testing. As a result of this successful surveillance initiative, the McMaster University Molecular Diagnosis Laboratory has expanded its diagnostic service to include molecular testing. Molecular testing allows confirmation of diagnosis in deceased patients and reliable carrier testing in families with known mutations. To date, the diagnosis has been confirmed in three deceased patients on whom no biochemical testing was performed, and 14 new patients have been genotyped. SLO is caused by a generalized cholesterol deficiency resultant from an inherited biochemical defect that causes decreased production of cholesterol from its immediate precursor, 7-dehydrocholesterol (7DHC). SLO ranges from mildly abnormal facial features, with mental retardation and significant behavioural abnormalities, to severe birth defects causing stillbirths and miscarriages. SLO is diagnosed by demonstrating elevated 7DHC in plasma or in amniotic fluid. Sixty-seven different SLO mutations have been identified since the gene for SLO, called DHCR7, was found in 1998.

45. Smith-Lemli-Opitz Syndrome I (David W. Smith) (www.whonamedit.com)
SmithLemli-opitz syndrome I (David W. Smith) A syndrome of multiple abnormalities,comprising mental retardation, microcephaly, growth retardation
http://www.whonamedit.com/synd.cfm/1720.html

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Smith-Lemli-Opitz syndrome I (David W. Smith) Also known as:
Smith's syndrome
Synonyms: Cerebrohepatorenal syndrome, genito-palato-cardial syndrome, RSH syndrome, SLO syndrome. Associated persons: Luc Lemli John Marius Opitz David Weyhe Smith Description: A syndrome of multiple abnormalities, comprising mental retardation, microcephaly, growth retardation, hypoplastic external genitalia and a characteristic facies with micrognathia and anteverted nostrils. Onset in fetal life; feeble fetal activity; at birth short stature. Cardiac, renal and vertebral abnormalities may be present. The eyes may show strabismuss, cataracts and ptosis.The condition is potentially lethal in infancy and survivors have severe mental retardation. Inheritance is autosomal recessive. Smith, Lemli, and Opitz in 1964 described the disease picture in three unrelated boys. The authors later termed the disease picture RHS syndrome from the initial letters of the family names of the described patients.

46. Herrmann-Opitz Syndrome I (www.whonamedit.com)
Herrmannopitz syndrome I A severe developmental anomaly with mental retardation,acrocephalosyndactyly and long list of other abnormalities. Who named it?
http://www.whonamedit.com/synd.cfm/1713.html

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Whonamedit.com does not give medical advice.
This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor.
Herrmann-Opitz syndrome I Associated persons:
Jürgen Herrmann

John Marius Opitz
Description: A syndrome of mental retardation and acrocephalosyndactyly (German: Turri-Brachyzephalie), peculiar facies similar to Saethre-Chotzen syndrome, pronounced hypertelorismus, small chin, deep dysmorphic ears, cryptorchism, limitation of movement of the elbows, brachysyndactyly of fingers and toes with lack of fourth finger, and various associated abnormalities. Herrmann and Opitz in 1969 reported the condition in a boy whose parents and five siblings were normal. Bibliography:
  • J. Herrmann, J. M. Opitz:

47. Smith-Lemli-Opitz Syndrome Information Diseases Database
SmithLemli-opitz syndrome,7-Dehydrocholesterol reductasedeficiency, Disease Database Information.
http://www.diseasesdatabase.com/ddb12223.htm
Diseases Database Index Sponsors Contact ... Previous Page
Smith-Lemli-Opitz syndrome Information
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2 synonyms or equivalents were found. Smith-Lemli-Opitz syndrome
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7-Dehydrocholesterol reductase deficiency Smith-Lemli-Opitz syndrome: Definition(s) via UMLS Code translations and terms via UMLS Smith-Lemli-Opitz syndrome: specific sites Send Smith-Lemli-Opitz syndrome to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these:
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48. Opitz Syndrome ? What Does Everyone Want To Know About Opitz Syndrome? Here's A
About opitz syndrome What you and I might want to know. Recommended Referencesand Products. Earlier Blogs To NOV 10 2002. Latest books on opitz syndrome
http://health.xq23.com/conditions/part_2/Opitz_syndrome.html
About Opitz syndrome : What you and I might want to know.
Recommended References and Products. [see index for total category]
Books:

X-Linked Mental Retardation
by John M. Opitz
X-Linked Mental Retardation 3 : Proceedings of the Third International Workshop on Fragile X and X Linked Mental Retardation Held in Troina, Italy Se
by John M. Opitz
X-Linked Mental Retardation 2: Proceedings of the Second International Workshop on Fragile X and X-Linked Mental Retardation Held on Dunk Island, aut
by John M. Opitz
The Rett Syndrome
by John M. Opitz
Serendipity Driven Links and Topics:
http://members.aol.com/slo97/

http://www.apollos.net/arena/opitz/definition.html

http://rkymtnhi.com/opitz/
http://www.emedicine.com/ped/topic2117.htm ... http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome498.html Latest books on: Opitz syndrome PUBMED Citations: DVD Videos: by James Goldstone by James Goldstone The China Syndrome by Jane Fonda The Stendhal Syndrome by Asia Argento VHS Videos: Asperger's Syndrome Video by The China Syndrome by Jane Fonda Omega Syndrome by Joseph Manduke Ebola Syndrome by Herman Yau Omega Syndrome by Ken Wahl Star Trek - The Original Series, Episode 48: The Immunity Syndrome

49. Smith Lemli Opitz Syndrome
Smith Lemli opitz syndrome. Disorder Subdivisions. None. General Discussion.SmithLemli-opitz syndrome is a hereditary developmental disorder.
http://www.meritcare.com/hwdb/showTopic.asp?pd_hwid=nord292

50. Genetic Disorders: Opitz Syndrome
Genetic Disorders opitz syndrome. National Library of Medicine OS. opitz syndrome,the synonyms, a summary and a list of major features. NORD opitz syndrome.
http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/Op
Genetic Disorders: Opitz Syndrome
Home Health Conditions and Diseases Genetic Disorders : Opitz Syndrome google_ad_client = 'pub-3272565765518472';google_ad_width = 336;google_ad_height = 280;google_ad_format = '336x280_as';google_color_border = 'FFFFFF';google_color_bg = 'FFFFFF';google_ad_channel ='7485447737';google_alternate_color = 'FFFFFF';google_color_link = '0000FF';google_color_url = '008000';google_color_text = '000000';
Standard Listings
Canadian Opitz Family Network
A description of Opitz G/BBB Syndrome.
Family Village
Opitz G Syndrome information and contact links.
National Library of Medicine: OS
Opitz syndrome, the synonyms, a summary and a list of major features.
NORD: Opitz Syndrome
A look at the alternate names, a general discussion and resources.
The Opitz G/BBB Family Network
Online support and information for families with Opitz G/BBB Syndrome. Provides families with easy-to-read information about the syndrome.
Zach's Opitz Syndrome Site
Offers information, a family's experience with this syndrome and links to the Opitz Family Network.
Help build the largest human-edited directory on the web.

51. Genetic Disorders: Smith Lemli Opitz Syndrome
Genetic Disorders Smith Lemli opitz syndrome. Home Health Conditions and DiseasesGenetic Disorders Smith Lemli opitz syndrome. Smith Lemli opitz syndrome.
http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/Sm
Genetic Disorders: Smith Lemli Opitz Syndrome
Home Health Conditions and Diseases Genetic Disorders : Smith Lemli Opitz Syndrome google_ad_client = 'pub-3272565765518472';google_ad_width = 336;google_ad_height = 280;google_ad_format = '336x280_as';google_color_border = 'FFFFFF';google_color_bg = 'FFFFFF';google_ad_channel ='7485447737';google_alternate_color = 'FFFFFF';google_color_link = '0000FF';google_color_url = '008000';google_color_text = '000000';
Standard Listings
Emergency Medicine
An extensive article about Smith-Lemli-Opitz syndrome, a multiple congenital anomalies/mental retardation syndrome caused by a defect in cholester...
NORD: Smith Magenis Syndrome
Offers the synonyms, a general discussion and further resources.
Smith Lemli Opitz Syndrome
Advocacy and exchange. Includes a detailed description, diagnosis, the natural history, biochemistry, genetics, treatment and contact details.
Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor PureDirectory.com uses a modified version of the Open Directory.

52. Health Library -
Smith Lemli opitz syndrome. Synonyms Disorder Subdivisions General DiscussionResources SmithLemli-opitz syndrome is a hereditary developmental disorder.
http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

53. Smith – Lemli – Opitz Syndrome
Smith – lemli – opitz syndrome,. Print this article, (David W. Smith,20th century, American paediatrician; Luc Lemli, 20th century
http://www.amershamhealth.com/medcyclopaedia/Volume VII/SMITH LEMLI OPITZ SYND
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Smith – lemli – opitz syndrome, (David W. Smith, 20th century, American paediatrician; Luc Lemli, 20th century, American paediatrician; John M. Opitz, 20th century, American paediatrician), syndrome with autosomal recessive inheritance in which children present with multiple congenital abnormalities in association with low birth weight and mental retardation. There is failure to thrive and progressive spasticity in childhood. Urogenital abnormalities with ambiguous genitalia may occur. Two forms are described: type I, which presents in childhood and type II, in which there may be intrauterine growth retardation. Radiological manifestations are microcephaly, which may be associated with multiple other brain malformations, soft tissue syndactyly of the toes and nonspecific urinary tract abnormalities.
HC
The Encyclopaedia of Medical Imaging Volume VII Contacts GE Healthcare Making Waves

54. Smith Lemli Opitz Syndrome
Smith lemli opitz syndrome,. Print this article, (David W. Smith, 20thcentury, American paediatrician; Luc Lemli, 20th century, American
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/Smith Lemli Op
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Smith lemli opitz syndrome, (David W. Smith, 20th century, American paediatrician; Luc Lemli, 20th century, American paediatrician; John M. Opitz, 20th century, American paediatrician), syndrome with autosomal recessive inheritance in which children present with multiple congenital abnormalities in association with low birth weight and mental retardation. There is failure to thrive and progressive spasticity in childhood. Urogenital abnormalities with ambiguous genitalia may occur. Two forms are described: type I, which presents in childhood and type II, in which there may be intrauterine growth retardation. Radiological manifestations are microcephaly, which may be associated with multiple other brain malformations, soft tissue syndactyly of the toes and nonspecific urinary tract abnormalities.
HC
The Encyclopaedia of Medical Imaging Volume VII
Contacts
GE Healthcare Making Waves

55. Clinical Trial: Prenatal Screening For Smith-Lemli-Opitz Syndrome
Prenatal Screening For SmithLemli-opitz syndrome. This study is currently recruitingpatients. Condition, Phase. Smith-Lemli-opitz syndrome Pregnancy, Phase II.
http://www.clinicaltrials.gov/ct/gui/show/NCT00070850?order=39

56. Clinical Trial: Study Of Smith-Lemli-Opitz Syndrome
Study of SmithLemli-opitz syndrome. Official Title Clinical and Basic Investigationsinto Smith-Lemli-opitz syndrome. Further Study Details
http://www.clinicaltrials.gov/ct/gui/show/NCT00001721?order=34

57. :: Ez2Find :: Opitz Syndrome
Guide opitz syndrome, Global Metasearch Any Language Guides, opitz syndrome.ez2Find Home Directory Health
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58. :: Ez2Find :: Smith Lemli Opitz Syndrome
Guide Smith Lemli opitz syndrome, Global Metasearch Any Language Guides,Smith Lemli opitz syndrome. ez2Find Home Directory Health
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59. Kennedy Krieger Institute Smith-Lemli-Opitz Syndrome
KKI Logo. Print this page. SmithLemli-opitz syndrome. SLOS is a genetic disorderthat affects the development of children both before and after birth.
http://www.kennedykrieger.org/kki_diag.jsp?pid=1104

60. Opitz Syndrome
Home Health Conditions and Diseases Genetic Disorders opitz syndrome (6)See Also Family Village Opitz G Syndrome information and contact links.
http://www.thenewhealthfind.com/Health/ConditionsandDiseases/GeneticDisorders/Op
Directory Home Health Conditions and Diseases Genetic Disorders : Opitz Syndrome (6)
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