61. Portal Toolkit Invalid Site URL Pfeiffer syndrome, SaethreChotzen syndrome, Carpenter syndrome and Cohensyndrome (craniofrontonasal dysplasia) and many other eponymous conditions, http://ppv.ovid.com/pt/re/aunz/fulltext.00130494-200311000-00024.htm

Sorry, the URL specified, http://ppv.ovid.com:80/pt/re/aunz/fulltext.00130494-200311000-00024.htm , is invalid. To go to site for "OvidPPV" please click here http://ppv.ovid.com To go to site for "ANZ Journal of Surgery" please click here http://www.lwwonline.com To go to the LWW Online site, please click here http://www.lwwonline.com Thank you

62. Orthopaedic Syndromes First Page Craniofacialdeafness-hand syndrome craniofrontonasal dysplasia Craniometaphyseal dysplasia Craniosynostosis, Adelaide type Craniosynostosis, http://freeortho.com/syndromes.html

Orthopaedic Related Syndromes Orthopaedic related syndromes are listed below in alphabetical order. Click on the syndromes for further details: A B C D ... H I J K L M ... P Q R S T U V W X Y Z OMIM Database ALL Syndromes - Clinical Features University of Western Ontario - Paediatric Database Gene maping and Other details: Achondrogenesis Ib Achondrogenesis-hypochondrogenesis, type II Achondroplasia Acrocallosal syndrome ... XLA and isolated growth hormone deficiency

63. HEALTHMEDNET ILLNESS DISEASE URL DIRECTORY craniofrontonasal dysplasia. http//directory.ansme.com/health/168.html.craniofrontonasal dysplasia. http//my.webmd.com/content/healthwise/30/7398 http://www.healthmednet.com/COO-CRI.htm

64. Sydney Children's Hospital - Directory Of Services Craniofacial syndromes such as hemifacial microsomia, Treacher Collins, Binder,craniofrontonasal dysplasia, Down syndrome. Rare craniofacial clefts. http://www.sch.edu.au/services/services.asp?id=69

65. ABC-Dir: Php Nord NORD craniofrontonasal dysplasia (Popularity ) (Score 8.56) Offers a generaldiscussion and resources. Category Main\Health\Conditions and http://www.abc-directory.com/view/php_nord/

Home Set as Homepage Add to Favorite Contact 08 September, 2005 egories Arts Business Computers Games ... Sports Sites: php nord Sites Records 1-15 Go to page Newspaper cuttings from Radio Nord (Popularity: ) (Score: 12.34) Radio Nord operated in 1961-1962 off Sweden. Read what the newspapers wrote about the station. Category: NORD Mining Safety (Popularity: ) (Score: 11.53) NORD mining safety equipments, producer of NordLamp explosionproof miners caplamps Category: Club VTT Du Nord-Ouest, Inc. (Popularity: ) (Score: 11.53) Information about the Club, VTT du Nord-Ouest, located in Edmundston, New Brunswick, its trails and activities. Category: NORD: Spasmodic Dysphonia (Popularity: ) (Score: 11.29) Abstracted version of a report from National Organization for Rare Disorders database. Features include a general description of SD, listings ... Category: Dercum Disease (NORD article) (Popularity: ) (Score: 11.10) A short discussion about this rare disorder (aka Dercum's Disease, Adiposis Dolorosa), characterized by pressure of fatty deposits on nerves, ... Category: NORD (National Organization for Rare Disorders) (Popularity: ) (Score: 10.68)

66. Craniofrontonasal Syndrome (CNFS) Synonyms, craniofrontonasal dysostosis. craniofrontonasal dysplasia (CFND).Summary, Fontonasal dysplasia, coronal craniosynostosis, grooved nails, http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome252.html

Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome craniofrontonasal syndrome (CNFS) Synonyms craniofrontonasal dysostosis craniofrontonasal dysplasia (CFND) Summary Fontonasal dysplasia, coronal craniosynostosis, grooved nails, mild mental deficiency, and various skeletal and soft tissue abnormalities. Major Features Head and neck: Coronal suture synostosis, brachycephaly, frontal bossing, and facial asymmetry. Eyes: Soft tissue hypertelorism, increased bony interorbital distance and occasional strabismus, and downslanting palpebral fissures. Nose: Bifid nose with broad tip. Mouth and oral structures: Highly arched palate, cleft lip and/or palate, and malocclusion. Neck: Webbed. Thorax: Pectus excavatum. Abdomen: Diaphragmatic hernia. Hand and foot: Broad first toe, short first fingers, brachydactyly, clinodactyly, and gaps between the first and second toes, long fingers and toes. Transverse palmar crease is the main dermatoglyphic defect. Extremities: Sprengel shoulder, narrow sloping shoulders, hyperextensible joints Spine: Scoliosis.

67. The Cleft Palate-Craniofacial Journal craniofrontonasal dysplasia, Abstract Print Version. craniosynostosis,Abstract Print Version. craniosynostosis, Abstract Print Version http://cpcj.allenpress.com/cpcjonline/?request=get-keyword-index&issn=1545-1569&

68. The EyePathologist Disease - C craniofrontonasal dysplasia Klintworth, Gordon K. Craniofrontonasal syndrome -Klintworth, Gordon K. Craniopharyngioma - Klintworth, Gordon K. http://www.eyepathologist.com/LIST.ASP?Title=C

69. Craniofrontonasal Dysplasia Charles Davis is a Plastic, Reconstructive and CranioMaxillofacial Surgeon.He specialises in treating craniofacial malformations and complex ear and http://www.craniofacialsurgery.co.nz/craniofacial.html

Craniofrontonasal dysplasia Also previously known as Cohen syndrome. A coronal craniosynostosis is present and this is treated in the first year of life. The eyes are widely spaced (hypertelorism) and this is corrected using a facial bipartition at about age 8. The maxillary occlusal plane is often convex and this is corrected concurrently. Frequently the nasal tip is very broad or bifid and this is also corrected. Back to page Craniofacial Surgery Ear Reconstruction Maxillofacial Surgery ... Skin Cancer

70. Links: - Alabama Council For Developmental Disabilities Fibrous Dysplasia Support Online For those seeking support and information Costello Syndrome craniofrontonasal dysplasia Cri du Chat Syndrome http://www.acdd.org/Links/conditions/Rare_Disorders.htm

Skip to content You are here: Home Links Conditions Rare Disorders Rare Disorders G rants Council In f ... me On this page: General Disorders General Cherubs - A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. Contact a Family - Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. Fibrous Dysplasia Support Online - For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism. Human Growth Foundation - Information about growth-related disorders through education, research, and advocacy. Member driven organization. International Rare Disease Support Network - A community providing more than a 1000 different links to support groups for the people of all nations. Kindler Syndrome - An article and case study of this rare disease. Includes links. National Organization for Rare Disorders, Inc.

71. Clinical Genetics Congenital Pain Insensitivity@ (2); Cornelia De Lange Syndrome@ (2);Costello Syndrome (2); Cowden Syndrome (3); craniofrontonasal dysplasia (3) http://www.perinatology.com/genetics.htm

perinatology.com Genetics Directory Search Site Map Agencies and Organizations Calculators Critical Care Exposures Chemicals Drugs Infection Physical Agent ... Ultrasound See Also: Genetic Counselor's Toolbox California DHS Genetic Disease Branch GeneClinics is a medical knowledge base relating genetic testing to the diagnosis, management, and genetic counseling of individuals and families with specific inherited disorders. Angelman Syndrome GeneClinics Beckwith-Wiedemann Syndrome GeneClinics Muscular Dystrophy GeneClinics Fragile X Syndrome GeneClinics Phenylalanine Hydroxylase Deficiency (PKU) GeneClinics Prader-Willi Syndrome GeneClinics Smith-Lemli-Opitz Syndrome GeneClinics Tuberous-Sclerosis GeneClinics Genetic Analysis Software Rockefeller University The Gene Letter Genetic Education Materials (GEM) Database Searchable listing of public health genetics policy documents and clinical genetics educational materials Information For Genetic Professionals University of Kansas Medical Center International Birth Defects Information Systems Online Mendelian Inheritance in Man OTIS Organization of Teratology Information Services Pediatric Database Description of pediatric conditions.

72. JustCan.com Disability Directory Costello Syndrome@ (2); craniofrontonasal dysplasia@ (3) Fibrous DysplasiaSupport Online - For those seeking support and information concerning http://directory.justcan.com/odpphp/odp.php?browse=/Health/Conditions_and_Diseas

73. D Lindhout Publications craniofrontonasal dysplasia genetic heterogeneity? (letter). Clin Genet 1984;2680.10. Lindhout D, Meinardi H. Spina bifida and inutero exposure to http://humgen.med.uu.nl/addresses/people/curriculum/Lindhout pubs.html

Publications by D. Lindhout, M.D., Ph.D. CONTENTS I Articles in international peer-reviewed scientific journals II Articles in Dutch peer-reviewed journals III Chapters in books (English) IV Chapters in books (Dutch) ... VI Educational articles last updated October 2002 I Articles in international peer-reviewed scientific journals 1. Lindhout D, Barth PG, Valk J, Boen-Tan TN. The Joubert syndrome associated with bilateral chorioretinal coloboma. Eur J Pediatr 1980;134:173-176. 2. Lindhout D. The Joubert syndrome associated with bilateral chorioretinal coloboma (letter). Eur J Pediatr 1981;137:101-102. 3. Lindhout D, Meinardi H. False-negative pregnancy test in women taking carbamazepine (letter) Lancet 1982;ii:505. 4. Heimans JJ, Lindhout D, Huisman UW, Kwee ML, Visser SL, Whitton HW. H-reflex studies in a family with possibly X-linked neuronal Charcot-Marie-Tooth disease. Clin Neurol Neurosurg 1982;84:147-158. 5. Kwee ML, Lindhout D. Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression? Clin Genet 1983;24:200-205.

74. Information Center For Rare Diseases And Orphan Drugs craniofaciocervical osteoglyphic dysplasia craniofrontonasal dysplasiacraniofrontonasal syndrome teebi type craniometaphyseal dysplasia dominant type http://www.raredis.org/modules/sections/index.php?op=printpage&artid=25

75. Plast Reconstr Surg 2001 October;108(5):1316-1333. Copyright © 2001 American So Until the gene is found, craniofrontonasal syndrome can only be diagnosed Nicolaides, K., and Gosden, C. craniofrontonasal dysplasia in two male sibs. http://www.smiletrain.org/library/images/cleft206article.htm

Prenatal Sonographic Diagnosis of Major Craniofacial Anomalies Granger B. Wong , M.D., D.M.D. ; John B. Mulliken, M.D.; Beryl R. Benacerraf, M.D. Boston, Mass. From the Craniofacial Centre and the Division of Plastic Surgery at Children´s Hospital and the Department of Radiology at Massachusetts General Hospital, Harvard Medical School. PLASTIC AND RECONSTRUCTIVE SURGERY 2001;108:1316-1333 [Click here for reference links. (112 references linked.)] Fetal ultrasonography has made antenatal medicine possible, a specialized field that includes prenatal diagnosis, epidemiology, fetal therapy, and altered delivery strategies. Approximately 4 to 5 percent of newborns have some kind of structural anomaly, either a malformation, deformation, or disruption. The incidence of anomalies is even higher by examination of aborted embryos or by ultrasonic evaluation of fetuses that are eliminated through natural selection (terathanasia). It is tacitly believed that infants with a craniofacial deformity are best cared for by an interdisciplinary team. The same coordinated care should also be available for unborn children with the expertise of a specialist such as a sonologist, obstetrician, perinatologist, geneticist, and appropriate surgeon. Parents may ask for advice from a plastic surgeon before conception because one of them has a familial craniofacial anomaly. More often, the plastic surgeon is called to consult after a fetal abnormality is discovered by ultrasonography. The parents need counsel on the feasibility of operative correction, number of procedures, expected outcome, and quality of life issues.

76. Connexion Genatlas name, craniofrontonasal dysplasia with coronalcraniosynostosis,hypertelorism,clefting of the nasal tip,grooved nails,abnormalitiesof the thoracic http://www.dsi.univ-paris5.fr/genatlas/phenotype.php?symbol=CFNS

77. Craniofrontonasal Dysplasia . Genetic Disorders . Conditions + A clinical synopsis of craniofrontonasal dysplasia. + syndrome, a summary anda list of features. ? http://www.thema-gute-gesundheit.de/Health|DE-6404-6640|Conditions,and,Diseases|

Craniofrontonasal Dysplasia . Genetic Disorders Conditions and Diseases Health Home Craniofrontonasal Dysplasia . Genetic Disorders . Conditions Diseases . Health Rare Disorders + case study of this rare disease. Includes links. + biosynthesis and pathophysiology of BH4 and tetrahydrobiopterin deficiency. + information and a personal account, including pictures and X-rays. Also offers patient contact and an email discussion group. + A clinical synopsis of Craniofrontonasal Dysplasia. + syndrome, a summary and a list of features.

78. The World Diseases A 2 Z Names By Countrylinks And Dr Impex craniofrontonasal dysplasia. Craniosynostosis. Creutzfeldt Jakob Disease.Crigler Najjar Syndrome. Crohn s Disease. Cryptosporidiosis http://www.countrylinks.biz/diseases.htm

Country Links Dr Impex free on-line Services Note: search with CTRL + F A Aarskog Syndrome Aase Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Achilles Tendonitis Achondroplasia Acoustic Neuroma Acromegaly Activated Protein C Resistance Acute Idiopathic Polyneuritis ADD and ADHD Addiction and Recovery Addison's Disease Adiposis Dolorosa Adjustment Disorders Adrenoleukodystrophy Agnosia Agoraphobia Aicardi Syndrome AIDS Alagille Syndrome Albinism Alcoholism Alexander Disease Alkaptonuria Allergies Alopecia Alpers' Disease Alpha1 Antitrypsin Deficiency Alport Syndrome Alstrom Syndrome Alternating Hemiplegia Altophobia Alzheimer's Amblyopia Amputee Amyloidosis Amyoplasia Congenita Amyotrophic Lateral Sclerosis Anal Fissures Anemia Anencephaly Aneurysm Angina Pectoris Anophthalmos Anorexia Anosmia Anterior Knee Pain Syndrome Antiphospholipid Syndrome Anxiety Aortic Valve Disease Apert Syndrome Aphasia Aplastic Anemia Apnea, Sleep Appendicitis Arrhythmia Arteriohepatic Dysplasia Arthritis Arthrogryposis Asbestosis Asperger's Syndrome Aspergillosis Asthma Atherosclerosis Athlete's Foot Atrial Fibrillation Attachment Disorder Attention Deficit Disorder Autism Auto Immune Disorders Aviophobia Aviatophobia B Bacillary Angiomatosis Back Disorders Bad Breath Balanitis Baldness Barth Syndrome Bassen Kornzweig Syndrome Batten Disease Beckwith-Wiedemann Syndrome Behcet's Syndrome Bell's Palsy Benign Breast Lumps Benign Prostatic Hyperplasia Berger's Disease Beriberi Beryllium Disease

79. Fundación Comité Español De Los Colegios Del Mundo Unido Translate this page craniofrontonasal dysplasia associated with agenesis of Corpus Callosum.Pediatria Catalana, vol.63, 2003. Pg. 78-80. - Alonso PL, Sacarlal J, Aponte JJ, http://www.colegiosmundounido.org/lafundacion/CV4.htm

Enrique (Quique) Bassat Orellana Febrero-Junio 2004 Facultad de medicina Beca de los Colegios del Mundo Unido EXPERIENCIA Octubre 2004-Actualmente Junio 2000-Junio 2004 Septiembre 2002-Actualmente -Vocal de la junta directiva, consultor medico. Junio-Octubre 2003 M026de la vacuna candidata de la malaria RTS,S/AS02 Enero-Febrero 1999 Julio-Agosto 1998 -Trabajo de campo supervisado por el Dr. Pedro Luis Alonso 1993-Actualmente -Miembro del equipo organizador de la ceremonia de apertura -Voluntariado social con enfermos terminales de SIDA a ancianos y discapacitados visuales -Unidad de guardacostas y salvamento en acantilados -Diploma de primeros auxilios OTROS - Participante en la ceremonia de apertura de las Olimpiadas de Barcelona 1992 . PUBLICACIONES - Enrique Bassat, Dominique Vizmanos, Jordi Almar, Salvador Salcedo. Craniofrontonasal Dysplasia associated with agenesis of Corpus Callosum. Pediatria Catalana, vol.63, 2003. Pg. 78-80.

80. LOGOS Týp Yayýncýlýðý craniofrontonasal dysplasia is a rare Xlinked disorder that maps to 13cM regionon Xp22. Phenotypic features include craniosynostosis, brachiocephali, http://www.logos.com.tr/tr/p_sendrom44.asp

KREDÝLENDÝRME DENEME SINAVI Editörden ... Arþiv AYLIK AKTÜEL TIP DERGÝSÝ / MAYIS 2005 ANESTEZÝYOLOJÝ VE REANÝMASYON Hasta bilgilendirmenin önemi, 17(5):36-53, 2005 Prof. Dr. M. Erdal Güzeldemir GATA Anesteziyoloji ve Reanimasyon Anabilim Dalý ÖZET SUMMARY Hipokrat'ýn; dürüst, güvenilir ve iyi niyetli; "Beyaz Gömlekli Tanrýlar'ý, hekimler, geliþen insanoðlunun bakýþ açýsýndaki önemli deðiþiklikler nedeni ile, günümüzde artýk o yüce makamýndan oldukça farklý bir düzeyde yerini almýþtýr. Paternalist(babacý) davranýþ yaklaþýmýndan feragat etmek zorunda býrakýlan hekime, hastaya "gereken bilginin verilmesi" gibi, oldukça yeni ve kavramada hala güçlük çekilen, yeni bir etik ödev yüklenmiþtir. Temel insan haklarýndan olan, elde etmek için çok uzun uðraþýlar verilen bireyin kendi hakkýnda karar verme hakký "kendi kaderini belirleme hakký", günümüzde çok öncelikli bir konuma yerleþmiþtir. "Kendi kaderini belirleme hakký", hastanýn bilgilendirilerek, konu hakkýnda aydýnlatýlarak, kendisine tanýnan seçenekler arasýndan seçim yapabilmesine olanak tanýmaktadýr. Geliþmiþ toplumlarda çok önceleri baþlayan tartýþmalar ile, çok ileri düzeyde kazanýlan ve kurumsal tabana oturtulan haklar, yurdumuzda 1998 yýlýnda yürürlüðe giren Hasta Haklarý Yönetmeliði'yle güncelimize taþýnmýþ oldu; ''Hasta; saðlýk durumu, kendisine uygulanacak týbbi iþlemler, bunlarýn faydalarý ve muhtemel sakýncalarý, hastalýðýn seyri ve neticeleri konusunda sözlü veya yazýlý olarak bilgi istemek hakkýna sahiptir."

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