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Opitz Syndrome:     more books (17)

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

lists with details

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

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

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
    
    Extractions: 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
    
    Extractions: 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. 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.

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
    
    Extractions: 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. 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.

47. Smith-Lemli-Opitz Syndrome Information Diseases Database
    SmithLemli-opitz syndrome,7-Dehydrocholesterol reductasedeficiency, Disease Database Information.  
    http://www.diseasesdatabase.com/ddb12223.htm
    
    Extractions: 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:

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

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
    
    Extractions: 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';

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
    
    Extractions: 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';

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
    
    Extractions: 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.

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
    
    Extractions: 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.

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  
    http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
    
    Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode

58. :: Ez2Find :: Smith Lemli Opitz Syndrome
    Guide Smith Lemli opitz syndrome, Global Metasearch Any Language Guides,Smith Lemli opitz syndrome. ez2Find Home Directory Health  
    http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
    
    Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Smith Lemli Opitz Syndrome Web Sites Emergency Medicine [Site Info] [Translate] [Open New Window] An extensive article about Smith-Lemli-Opitz syndrome, a multiple congenital anomalies/mental retardation syndrome caused by a defect in cholesterol synthesis. URL: http://www.emedicine.com/ped/topic2117.htm

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

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