41. Malattie Rare E Genetiche Lettera "M" Translate this page érable, maladie du••{} * MALATTIA DI GAUCHER•Gaucher disease•Gaucher, maladie de•Marfan,Síndrome de•{154700}•D•A * marie-sainton Sindrome di http://utenti.lycos.it/fmfpc/M.htm

HOME FORUM Site Map / Mappa del sito FMFPC's International Guest/Book ... E-mail Dal 22 Marzo 2003 il server Lycos, che ospita le pagine FMFPC, subirà un *fermo tecnico*. Le pagine resteranno accessibili ma non verranno aggiornate per circa una settimana. - Tutti i servizi di FMFPC continueranno a funzionare. - È ora possibile accedere al sito anche attraverso l'indirizzo alternativo di FMFPC (sito mirror) all'URL http://digilander.libero.it/fmfpc/portale.htm ultimi aggiornamenti Elenco malattie rare e genetiche"lettera M" © FMFPC è un sito ideato, realizzato ed aggiornato da un malato di FMF (Febbre Mediterranea Familiare) © FMFPC is a site conceived, realized and updated by a patient of FMF (Familial Mediterranean Fever) aggiornato 5 marzo, 2003 Cerca nel menu aree FMFPC AREE FMFPC Malattie Rare Febbre Mediterranea Familiare Laboratori Diagnosi Genetica Associazioni Malati Disabilità/Handicap Categorie Medicina (Directory) Ricerche WEB (Medicina) FMFPC è partner AidWeb.org Cerca nel sito / Search in this site I contatti fino ad oggi possibili con FMFPC: Cerca in questa pagina / Search in this page con i tasti / with the keys Ctrl+F A B C D ... L - M - N O P Q ... legenda M Maaswinkel Mooij Stokvis Brantsma Sindrome di Maaswinkel mooij stokvis brantsma syndrome de MacDermot Patton Williams Sindrome di Mac dermot patton williams syndrome de[Hypertrichose cubitale petite taille] ... Machado-Joseph, maladie de[Ataxie spinocérébelleuse autosomique dominante/ Ataxie cérébelleuse autosomique dominante]

42. Malattie Rare E Genetiche Lettera "S" Translate this page diDisostosi cleido-cranica••Scheuthauer-marie-sainton syndrome•••{}Schiel Malattia di Sindrome di•Schindler disease•Schindler, maladie de http://utenti.lycos.it/fmfpc/S.htm

HOME FORUM Site Map / Mappa del sito FMFPC's International Guest/Book ... E-mail Dal 22 Marzo 2003 il server Lycos, che ospita le pagine FMFPC, subirà un *fermo tecnico*. Le pagine resteranno accessibili ma non verranno aggiornate per circa una settimana. - Tutti i servizi di FMFPC continueranno a funzionare. - È ora possibile accedere al sito anche attraverso l'indirizzo alternativo di FMFPC (sito mirror) all'URL http://digilander.libero.it/fmfpc/portale.htm ultimi aggiornamenti Elenco malattie rare e genetiche "lettera S" © FMFPC è un sito ideato, realizzato ed aggiornato da un malato di FMF (Febbre Mediterranea Familiare) © FMFPC is a site conceived, realized and updated by a patient of FMF (Familial Mediterranean Fever) aggiornato 28 febbraio, 2003 Cerca nel menu aree FMFPC AREE FMFPC Malattie Rare Febbre Mediterranea Familiare Laboratori Diagnosi Genetica Associazioni Malati Disabilità/Handicap Categorie Medicina (Directory) Ricerche WEB (Medicina) FMFPC è partner AidWeb.org Cerca nel sito / Search in this site I contatti fino ad oggi possibili con FMFPC: Cerca in questa pagina / Search in this page con i tasti / with the keys Ctrl+F A B C D ... R - S - T U V W ... legenda S Saal Bulas Sindrome di Saal bulas syndrome de Saal Greenstein Sindrome di Saal greenstein syndrome de ... Saethre Chotzen Syndrome [SCS]/ Saethre-Chotzen syndrome [SCS Saethre-Chotzen, syndrome de

43. King Edward Memorial Hospital - Departments: Radiology - Case Of The Month 26_20 Synonyms Scheuthauermarie-sainton syndrome Cleidocranial dysostosis Mutationaldysostosis cardiomyopathy (arrhythmia), congenital heart disease (tetralogy). http://www.kem.edu/dept/radiology/case26_01.htm

Radiology Case of the Month Case No. : Month : February Year : Contributor : Dr. Zarine Shah Other Cases Case Report Discussion Radiological Features ... Differential Diagnosis Case report: Clinical Features A three-year-old child came to our hospital with the complaints of "a large depression in the front of the skull". The mental status and developmental milestones were normal. The child was otherwise clinically asymptomatic. Her older sib had similar complaints. Both children could touch their shoulders under their chin (Fig 1). Radiographs of the skull and chest were then performed (Fig 2, 3, 4). A routine skull radiograph frontal and lateral views shows an open anterior fontanelle and presence of Wormian bones. The chest radiograph shows absence of both clavicles. These findings on radiography led to the diagnosis of Cleidocranial dysplasia. The patient also had this abnormality. The three-year-old also had severe dental abnormalities. All these clinical findings with radiological evidence to support it helped to reach the diagnosis of Cleidocranial dysplasia. Discussion: Synonyms Scheuthauer-Marie-Sainton syndrome Cleidocranial dysostosis Mutational dysostosis Osteodental dysplasia Pelvicocleidocranial dysplasia .

44. DICCIONARIO DE TERMINOLOGIA MEDICA Translate this page Schaumann, síndrome de (también sarcoide de Boeck). • Schauthauer-marie-sainton,síndrome de. • Scheie, síndrome de. Seitelberger's disease II. http://www.iqb.es/Diccio/E/EponimoS.htm

A B C D ... Semon-Rosenbach, ley de (tambien, ley de Rosenbach-Semon) Senator, angina de Shulman, enfermedad de Sicard, tratamiento de Sicard, prueba de ... Siwe, enfermedad de e Smellie, maniobra de Smillie, prueba de Smirnoff, reflejo de Smith, enfermedad de ... Szent-Györgyi-Krebs, ciclo de

45. Med-kolleg.de Medizin Kolleg In Deutschland Medizin Tipps Arzt Krankenhaus Klini Translate this page M42.0 - Scheuermann-Krankheit Q74.0 - Scheuthauer-marie-sainton-Syndrom I82.9 9 -Sexualprobleme F52.9 - Sexualstörung A64 - Sexuell transmitted disease F52.1 http://www.arzt-notruf-hilfe.de/icd10/S/

Facharzt-Suche, Klinik-Suche Medizin-Lexikon und mehr Home Kliniksuche ICD-10 ICD – 10 ist eine internationale Klassifikation der Krankheiten. ICD – 10 SGB – V (die deutsche Fassung) wird in Deutschland als Schlüssel zur Angabe von Diagnosen, vor allem zur Abrechnung mit den Krankenkassen, verwendet. Informationen zu ICD-10* ICD10 Index: A B C D ... Den passenden Arzt oder Klinik finden mit HPN24 Praktizierende Ärzte in sind angehalten Diagnosen auf Rezepten und Krankenscheinen nur noch nach ICD-10 verschlüsselt anzugeben. ICD-10-SGBV, ICD-10-SGB-V In der vertragsärztlichen ambulanten Gesundheitsversorgung gilt für die Diagnosenverschlüsselung gemäß § 295 SGB V weiterhin die ICD-10-SGBV, Version 1.3 (Juli 1999). *Die Website kann Ihnen nur einen allgemeinen Überblick bieten und Orientierungshilfe sein. Allgemeine Informationen können Ihren Arzt nicht ersetzen, da nur er Ihre individuelle Situation beurteilen kann. Alle Angaben erfolgen ohne Gewähr. Die dargestellten Informationen dürfen auf keinen Fall als Ersatz für professionelle Beratung oder Behandlung durch approbierte Ärzte angesehen werden. Der Inhalt dieser Website ist ausschließlich für den Informationsgebrauch bestimmt. Die Informationen dürfen auf keinen Fall als Ersatz für professionelle Beratung oder Behandlung durch approbierte Ärzte angesehen werden. Allen Lesern wird geraten, bei Gesundheitsproblemen ihren Arzt aufzusuchen. Beim Auftreten von Ihre Gesundheit betreffenden Fragen sollten Sie immer mit Ihrem Arzt sprechen. Niemals sollte eine Behandlung eigenständig begonnen, geändert oder abgesetzt werden. Eine Verwendung der Information zur eigenständigen Stellung von Diagnosen oder zum Beginnen, Ändern oder Absetzen von Behandlungen ist unzulässig. Die Betreiber der Website können in keiner Weise - weder direkt noch indirekt - für Schäden oder Unannehmlichkeiten zur Verantwortung gezogen werden, die durch den Gebrauch oder Missbrauch der dargestellten Informationen entstehen.

46. Untitled disease (1) . craniofacial sysostosis (4) Apert syndrome acrocephalosyndactyly (5) marie-sainton syndrome - cleidocranial http://www.tmj-clinic.com/opendata/book/odqa/odqa20.htm

±¸°­Áø´ÜÇÐ QA Á¦ 20Àå 1. ÁõÈıº(syndrome)°ú Áúȯ(disease)À̶ó´Â ¿ë¾îÀÇ Á¤È®ÇÑ Á¤ÀÇ¿Í Â÷ÀÌÁ¡Àº? 3. À̵é "ÁõÈıº" Áß¿¡¼­ "Áúȯ"À¸·Î ¹Ù²î¾îÁø °ÍÀº? 4. Treacher Collins ÁõÈıºÀÇ ¹ß»ý ¿øÀÎÀº? 5. ´«ÀÇ ¾È°Ë¿­ÀÇ antimongoloid obliquity¶õ ? ... 27. ±¸°­³» Àü¾Ï º´¼Ò·Î °¡´É¼ºÀÌ ÀÖ´Â Plummer-Vinson ÁõÈıºÀÇ ÀÓ»ó ¼Ò°ß ¹× Áõ»ó, Ä¡·á¿¡ ´ëÇÏ¿©? <P. 464> À̵é "ÁõÈıº" Áß¿¡¼­ "Áúȯ"À¸·Î ¹Ù²î¾îÁø °ÍÀº? (2) žÆ(embryo)ÀÇ 50 mm stage ¶§, ¶Ç´Â ±× ÀÌÈÄ maxillary mesodermÀÇ ºÐÈ­°¡ Áö¿¬µÇ°Å³ª ½ÇÆÐÇÑ °á°úÀÌ´Ù. (4) 2Â÷ÀûÀ¸·Î ÇϾÇÀ» Çü¼ºÇÏ´Â visceral mesodermÀÇ first visceral archµµ °°Àº ±âÀüÀ¸·Î ºÐÈ­ Áö¿¬ÀÌ ¹ß»ýÇÑ´Ù. mongoloid obliquity antimongoloid obliquity (2) ÀÌ ÁõÈıºÀÇ ¸¹Àº ÇüÅÂÀû ÀÌ»óÀº ÇϾÇÀÇ ¹ßÀ° Á¤Áö·ÎºÎÅÍ ½À۵ȴÙ. Áï ÇϾÇÀÇ ¹Ì¹ß´Þ·Î Ư¡ÀûÀÎ "bird facies" ¾ç»óÀ» º¸ÀδÙ. (3) ÀÌ°ÍÀº Å»ý±â¿¡ palatal shelves »çÀÌ¿¡ ÀÖ´Â ÇôÀÇ Á¤»óÀûÀÎ ÇÏ°­À» ¹æÇØÇÏ°í ÀÌ·Î ÀÎÇØ ±¸°³¿­(cleft palate)ÀÌ ¹ß»ýÇÑ´Ù. (4) ÀÌ°ÍÀÌ Pierre Robin ÁõÈıº¿¡¼­´Â ±¸¼ø¿­(cleft lip)ÀÌ ³ªÅ¸³ªÁö ¾Ê´Â ÀÌÀ¯ÀÌ´Ù. (5) ¶ÇÇÑ ¼³Çϼö(glossoptosis)´Â Á¤»óÀûÀÎ ÇôÀÇ ±ÙÀ°µéÀ» ÇϾÇÀÌ æºÐÈ÷ ÁöÁöÇØÁÖÁö ¸øÇϱ⠶§¹®¿¡ ¹ß»ýÇÑ´Ù.

47. Pierre Marie (www.whonamedit.com) Marie's disease A rare chronic condition, usually caused by an adenoma. SchauthauerMarie-Saintonsyndrome A fairly common osseous anomaly with a long list of http://www.whonamedit.com/doctor.cfm/310.html

Home List categories Eponyms A-Z Biographies by country ... Contact Pierre Marie French neurologist, born September 9, 1853, Paris; died April 13. 1940, Paris. Associated eponyms: Bamberger-Marie disease A syndrome characterised by clubbing of the fingers and toes, periosteal new bone growth mainly, frequent evidence of joint involvement, and marked vasomotor disturbances involving hands and feet. Bekhterev's disease A chronic and progressive autoimmune disease characterized by arthritis, inflammation, and eventual immobility of a number of joints. Briquet's syndrome I A personality disorder in which alcoholism and somatisation disorder occur. Charcot-Marie-Tooth disease A syndrome characterized by slowly progressive wasting and weakness of distal muscle of the arms and feet, the commonest disease within a group of conditions called Hereditary Motor and Sensory Neuropathies (HMSN). Marie's anarthria Loss of ability to articulate words in persons with focal cerebral lesions. Marie's ataxia A hereditary disease of the nervous system, with cerebellar ataxia caused by bilateral cortical atrophy of the cerebellum. Marie's crossed adduction reflex Crossed, contralateral adductor reflex.

48. Syndrome DB - Table Of Contents syndrome marfanoid habitusmicrocephaly-glomerulonephritis syndrome Marie-Saintonsyndrome Marinesco X syndrome marker(22) Maroteaux-Lamy disease Maroteaux-Lamy http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_m.html

Multiple Congenital Anomaly/Mental Retardation Syndromes Table of Contents Return to Entry Page A B C ... Z M MacDermot-Winter syndrome macro-orchidism-marker X (MOMX) syndrome macrocephaly with feeblemindedness and encephalopathy with peculiar deposits macrocephaly-cutis marmorata telangiectatica congenita syndrome ... U.S. National Library of Medicine , 8600 Rockville Pike, Bethesda, MD 20894 National Institutes of Health Privacy Accessibility Last updated: 20 November 2001

49. S mucopolysaccharidosis V, forme fruste of Hurler's disease (.), ? 19? Scheuthauer Marie - Sainton, dysplasia cleidocranialis http://www.eksi.kz/consilium/librar/laz_s.htm

Ñèíäðîì Sabin Ñèíäðîì Sabouraud Ñèíäðîì Sahli Ñèíäðîì Saint ... Ñèíäðîì Schilder ^1 Ñèíäðîì Sabin, trias Sabin, ñèíäðîì Sabin - Feldman, pseudotoxoplasmosis. Sabin Albert Bruce (ðîä. 1906), àìåðèêàíñêèé âèðóñîëîã. Ñýáèíà ñ.- êëèíè÷åñêîå îáîçíà÷åíèå ñåðîíåãàòèâíîãî òîêñîïëàçìîçà (òàê íàçûâàåìîãî ïñåâäîòîêñîïëàçìîçà), ïðèçíàêè êîòîðîãî ñîîòâåòñòâóþò êàðòèíå êëàññè÷åñêîãî òîêñîïëàçìîçà: òðèàäà - ãèäðîöåôàëèÿ, õîðèîðåòèíèò è î÷àãè îáûçâåñòâëåíèÿ â ìîçãå. Êðîìå òîãî, íàáëþäàþò ýíîôòàëüì, ìèêðîôòàëüì, ñóäîðîãè. Ó äåòåé, áîëüíûõ òîêñîïëàçìîì, çàäåðæèâàåòñÿ óìñòâåííîå è ôèçè÷åñêîå ðàçâèòèå. ^2 Ñèíäðîì Sabouraud, ñèíäðîì Sabouraud - Prieur - Trenel, moniletrichosis. Sabouraud Raymond Jacques Adrien (1864-1938), ôðàíöóçñêèé äåðìàòîëîã. Ñàáóðî ñ.- êîìïëåêñ íàñëåäñòâåííûõ àíîìàëèé ñ ïåðåìåæàþùåéñÿ àïëàçèåé âîëîñ è ïîìóòíåíèåì õðóñòàëèêà (àóòîñîìíî-äîìèíàíòíîå, äîïóñêàåòñÿ òàêæå àóòîñîìíî-ðåöåññèâíîå íàñëåäîâàíèå): âîëîñû ðåäêèå ñ ïåðåìåæàþùåéñÿ àïëàçèåé; ÷àñòî-keratosis pilaris (íà ãîëîâå, áðîâÿõ, ïîä ìûøêàìè, íà áåäðàõ; èíîãäà íà âñåì òåëå), ïîìóòíåíèå õðóñòàëèêà. Äåòè ðîæäàþòñÿ ñ íîðìàëüíûì îâîëîñåíèåì, îäíàêî çàòåì âîëîñû ó íèõ âûïàäàþò è ïîçäíåå îòðàñòàþò î÷åíü íåðàâíîìåðíî. ^3 Ñèíäðîì Sahli, corona venosa Sahli. Sahli Hermann (1856-1933), øâåéöàðñêèé âðà÷. Ñàëè ñ. - ñèìïòîìîêîìïëåêñ ó áîëüíûõ ñ çàêóïîðêîé âåðõíåé ïîëîé âåíû (ïðåèìóùåñòâåííî â ñëó÷àÿõ îïóõîëè): â âåðõíåé ÷àñòè ãðóäíîé êëåòêè ðàñøèðåíû ïîäêîæíûå âåíû, ìåñòàìè îíè îáðàçóþò ñïëåòåíèÿ.

50. ICD-9-CM Disease Index: S 117.1; Scheuermann's disease or osteochondrosis 732.0; ScheuthauerMarie-Saintonsyndrome (cleidocranialis dysostosis) 755.59; Schilder http://www.cpmc.columbia.edu/homepages/hripcsa/icd9/2indexs.html

ICD-9-CM Index to Diseases: S Saber shin 090.5 tibia 090.5 Sac, lacrimal=see condition Saccharomyces infection (see also Candidiasis) 112.9 Saccharopinuria 270.7 Saccular=see condition Sacculation aorta (nonsyphilitic) (see also Aneurysm, aorta) 441.9 ruptured 441.5 syphilitic 093.0 bladder 596.3 colon 569.89 intralaryngeal (congenital) (ventricular) 748.3 larynx (congenital) (ventricular) 748.3 organ or site, congenital=see Distortion pregnant uterus, complicating delivery 654.4 affecting fetus or newborn 763.1 causing obstructed labor 660.2 affecting fetus or newborn 763.1 rectosigmoid 569.89 sigmoid 569.89 ureter 593.89 urethra 599.2 vesical 596.3 Sachs (-Tay) disease (amaurotic familial idiocy) 330.1 Sacks-Libman disease 710.0 [424.91] Sacralgia 724.6 Sacralization fifth lumbar vertebra 756.15 incomplete (vertebra) 756.15 Sacroiliac joint=see condition Sacroiliitis NEC 720.2 Sacrum=see condition Saddle back 737.8 embolus, aorta 444.0 nose 738.0 congenital 754.0 due to syphilis 090.5 Sadism (sexual) 302.84 Saemisch's ulcer 370.04 Saenger's syndrome 379.46

51. Les Mots Non Reconnus Dans La Nomenclature Meary 1715.9-MYOPATHIE CONGENITALE (CENTRAL CORE disease) MYOPATHIE A http://noemed.univ-rennes1.fr/htbin/reponse?prg=201&noment=meary

52. 100cia.com 100cia.com Noticias de ciencia comentadas y portal de contenidos científicos http://www.100cia.com/enlaces.php/Health/Conditions_and_Diseases/M

53. Infopage 1 Other names(synonyms) Cleidocranial Dysostosis, Osteodental Dysplasia (ODD), MarieSaintonDisease, Marie-saiton syndrome, Scheuthauer-marie-saiton syndrome http://cleidocranial_dysplasia.homestead.com/infopage1.html

Other names(synonyms): Cleidocranial Dysostosis, Osteodental Dysplasia (ODD), Marie-Sainton Disease, Marie-saiton syndrome, Scheuthauer-marie-saiton syndrome, cleidocranial digital dysostosis, craniocleidodysostosis, dysostosis cleidocranialis, dysostosis cleidocraniodigitalis, dysostosis cleidocraniopelvina, dysostosis generalisata, dysostosis cleidocranialis, pelvicocleidoctranial dysostosis, and Yunis-Varon Syndrome (YVS) Abbreviation is CCD. Living with a rare disorder Imagine your concern, knowing that something is wrong with you or a loved one, yet being unable to get a proper diagnosis. Living with a rare disorder can be a most disconcerting experience! Difficult to detect, there are often no tests to establish the fact that a specific disorder does indeed exist. More over, there are virtually no treatments or cures. Physicians, unless specializing in a particular rare disorder, seldom encounter any more than one or two cases in their medical careers. As such, this creates a greater need for more medical research and public awareness of the existence, cause and effects of rare disorders. When a rare disorder is suspected or is confirmed through medical diagnosis, the person affected will immediately seek help and support so as to properly understand and cope with the situation. However, more often than not, there is little assistance or information available to the person witht he rare disorder other than a brief paragraph in an out dated medical encyclopedia at the local library. Certainly little consolation to the sufferer who must contend with the disease for a life time.

54. M Website Results :: Linkspider UK Mannosidosis@ (2); Marburg@ (6); Marfan Syndrome@ (39); MarieSaintonDisease@ (6); Marinesco-Sjogren Syndrome@ (5); Mayer Rokitansky Kuster http://www.linkspider.co.uk/Health/ConditionsandDiseases/M/

M Websites from Linkspider UK Keyword: M Linkspider UK Directory M Search for Directory Tree: Top Health Conditions and Diseases : M (0) Add URL Advertise Here! Personalize Amazon ... Myotonic Dystrophy

55. M : Top : Health : Conditions And Diseases : M Malaria; Malnutrition; Mannosidosis; Marburg; Marfan Syndrome; MarieSaintonDisease; Mayer Rokitansky Kuster Hauser Syndrome; McArdle's http://www.theolympicsite.org/Top/Health/Conditions_and_Diseases/M/

Features Summer Winter Athens Torino Directory Arts Business Computers Games ... M Categories Machado-Joseph Disease Macular Degeneration MAC Mad Cow Disease ... Myotonic Dystrophy document.write(doClock("D1","%20","M1","%20","Y0")); Sponsors Arbot.com SimplyZip.com UnclaimedFunds.org Features Athens 2004 Torino 2006 Beijing 2008 Arbot Technology Group

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