21. Medizin-Lexikon Buchstabe D ICD-Code - Medizin-Service Von Regional-Info Translate this page Gleichgewichtsstörung, Darmflora Dyschezie Dyscholie Dyschromatopsie Dyschromie dysencephalia splanchnocystica Dysenterie Dyserythropoetische http://www.med-kolleg.de/icd/D.htm

Facharzt-Suche, Klinik-Suche Medizin-Lexikon und mehr Home Kliniksuche Apotheken Medizinisches Lexikon ... Medizin News Suche Suche nach Diagnose oder ICD10 A B C D ... Medizin Newsletter Registrieren Sie sich mit Ihrer eMail-Adresse und Sie erhalten unseren Medizin Newsletter Email-Adresse: Anmelden Abmelden Weitere Informationen... Sie sind hier: Medizin Ratgeber ICD10 Verzeichnis > D Medikament Bestellen FOCUS Gesundheit - Vor dem Bestellen vergleichen und sparen: 7000 rezeptfreie Medikamente schnell und verständlich im Überblick - mit aktuellen Preisen. http://medikamente.focus.msn.de Krankheitsbilder Buchstabe D D1-Trisomie-Syndrom Da-Costa-Syndrom Dabue [Ainhum] Dacryocystitis neonatorum ... Barmenia - Krankenversicherung Sie suchen nach einer preiswerten Krankenversicherung mit Kompaktschutz? Die Barmenia bietet Ihnen eine beitragsgünstige Alternative zur gesetzlichen Krankenversicherung. http://www.barmenia.de Krankenversicherung - TOPScout vergleicht Vergleichen Sie mit TOPScout die verschiedenen Anbieter der privaten Krankenversicherung. Ein Krankenversicherungsvergleich kann Ihnen unter Umständen viel Geld einsparen. http://www.finanzpfadfinder.de

22. Entrez PubMed Genetics of the Meckel syndrome (dysencephalia splanchnocystica). Hsia YE, BratuM, Herbordt A. MeSH Terms Abnormalities, Multiple/genetics*; Arm/abnormalities; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

23. Entrez PubMed Meckel Gruber syndrome (dysencephalia splanchnocystica). Bhandari B, Mandowara SL,Mehta R. Publication Types Case Reports. MeSH Terms Abnormalities, Multiple; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

24. Delv.co.uk: Dissociative Identity Disorder Websites In The UK identity disorder Diverticulitis Down Syndrome Drooling Dry Eye Duane RetractionSyndrome Dubowitz Syndrome Dwarfism dysencephalia splanchnocystica http://www.delv.co.uk/kqry/dissociative identity disorder

BOOKMARK DELV.CO.UK MAKE DELV.CO.UK MY HOME PAGE Results: 1 - 25 - UK Search for: dissociative identity disorder document.cookie="metasearch=1765832714.20480.0000"; "Becoming One" Completely documented triumph over childhood abuse and MPD. sponsored by http://www.swanpondpress.com/ (MetaSearch Picks) Buy Identity at B club At B club you can find Identity on DVD or Video at a great price! Thousands of other movies available! sponsored by http://www.bclub.co.uk (Mirago) ... of Attachment Theory - as applied to clinical practice Anxiety Disorders specifically the agoraphobias and obsessive compulsive disorders Dissociative Identity Disorder a long standing academic and clinical interest i New ideas and proposals for Therapeutic Communities, including the ... http://www.johnjolliffe.co.uk/id4.htm ATC ... Gail McGregor - Art Therapist BA (Hons) degree in Fine Art Teaching Certificate in Education MA in Special Education Needs PGD in Arts Psychotherapy Enrolled at Derby University PHD in Art Therapy (2002-2005) - Dissociative Identity Disorder with regards to Self Mutilation and Sexual Abuse http://www.arttherapyconsultation.co.uk/persmain.html

25. Birth Disorder Information Directory - M Meckel (Gruber) Syndrome (dysencephalia splanchnocystica) List ofSites. MeckelLike Syndrome See Cerebrorenodigital Syndrome. Medial http://www.bdid.com/defectm.htm

HOME M Machado Joseph Disease (Autosomic Dominant Spinocerebellar Ataxia, Autosomic Dominant Cerebellar Ataxia, Cerebelloolivary Atrophy, Olivopontocerebellar Atrophy, Pierre Marie Cerebellar Ataxia) List of Sites Macrencephaly List of Sites Macrocephaly List of Sites Macrodactyly/Megalodactyly Macrodactly of the Right Foot Macrodactyly of Both Hands and Foot Associated with Cutaneous Hemangiomata MEGALODACTYLY Macroglossia Macroglossia (Includes Ultrasounds and Photos) Also see Beckwith Wiedemann Syndrome Blomstrand Syndrome Congenital Hypothyroidism Mucopolysaccharidosis and Simpson Golabi Behmel Syndrome Macrogyria MACROGYRIA Asperger's Syndrome Macular Dystrophy Vitelliform See Best Disease/Macular Dystrophy Atypical MACULAR DYSTROPHY, ATYPICAL VITELLIFORM; VMD1 Macules Hereditary Congenital Hypopigmented and Hyperpigmented See Westerhof Beemer Cormane Syndrome Madelung's Deformity See Leri Weill Syndrome Majewski Syndrome See Short Rib-Polydactyly Syndrome, Type IV Mal de Meleda See Meleda Disease Male Pseudohermaphroditism Due to 5-Alpha-Reductase Deficiency See Pseudovaginal Perineoscrotal Hypospadias Due to Androgen Insensitivity See Androgen Insensitivity Syndrome Male Turner Syndrome See Noonan Syndrome Malignant Hyperthermia See Hyperthermia, Malignant

26. Neural Tube Defects been confusing P Meckel Gruber dysencephalia splanchnocystica Syndrome Images- Prenatal Diagnosis - H van der Slikke, MD Elevated maternal and amniotic http://ibis-birthdefects.org/start/ntdfact.htm

Tips for printing Neural Tube Defects (NTD) Anencephaly - Spina Bifida About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Etchings Includes Anencephaly Encephalocele Folic Acid or FA Hydrocephalus - Arnold Chiari - Allied Disorders Meningocele - Meningomyelocele - Meningoencephalocele Meckel or Meckel Gruber or Dysencephalia splachnocystica Neural Tube Defects NTD Spina Bifida A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Group [Spanish] [Ukrainian] [*][P] Folic Acid for the Prevention of Neural Tube Defects Policy Statement - American Academy of Pediatrics (1993). "NTDs are among the most common birth defects that result in infant mortality and serious disability ..." Knowledge and Use of Folic Acid by Women of Childbearing Age Requires Acrobat Reader JAMA Women's Health and MMWR report. Results of the 1998 March of Dimes Birth Defects Foundation sponsored Gallup Organization survey of 2115 women. Folic Acid National Campaign - CDC, March of Dimes ... National Campaign on Folic Acid - Gate Page Folic Acid for Healthy Babies Prevention Model and Resource Guide NTD - Frequently asked Questions " ... how can women get folic acid? ... "

27. GORM C10.S1.2004.19 MeckelGruber Syndrome (dysencephalia splanchnocystica) A Case Report with PrenatalDiagnosis and Postmortem Evaluation Süleyman ESERDAÐ1, Serdar CEYLANER2 http://www.mebas.com.tr/gorm 2004/GORM C10.S1.2004.16.htm

GORM Volume: 10 Number: 1 2004 Meckel-Gruber Syndrome (Dysencephalia Splanchnocystica): A Case Report with Prenatal Diagnosis and Postmortem Evaluation Süleyman ESERDAÐ1, Serdar CEYLANER2, Ýrfan TARHAN1, Sema ZENGEROÐLU3, Nuri DANIÞMAN1 Ankara-Turkey Because of the automosal recessive inheritance of disorder, prenatal diagnosis is quite important for genetic counselling of affected gestations in Meckel-Gruber Syndrome(MGS). We report a case of MGS presumptively diagnosed in midpregnancy by sonogpaphy. In postmortem evaluation occipital encephalocoele, low-set ears, flat nasal bridge, bilateral polycystic kidneys, hepatomegaly, and absence of atria in heart were confirmed the diagnosis. The chromosomal analysis was normal, 46 XX. The objective of this paper is to emphasize the importance of diagnosis prenatally and postmortem evaluation, and also review different variations of malformations of MGS. (Gynecol Obstet Reprod Med 2004; 10:62-63) Key Words: Prenatal diagnosis, Meckel-Gruber syndrome

28. GORM - Icindekiler MeckelGruber Syndrome (dysencephalia splanchnocystica) A Case Report with PrenatalDiagnosis and Postmortem Evaluation Süleyman Eserdag, Serdar Ceylaner http://www.mebas.com.tr/gorm 2004/GORM C10.S1.2004.htm

GORM Volume: 10 Number: 1 2004 Contents Analyses of Prenatally Diagnosed Fetal Talipes Cases Ýbrahim Serdar Serin, Mustafa Baþbuð, Bülent Özçelik, Mehmet Tayyar, Kayseri-Turkey Review of the Prenatally Diagnosed Ten Sacrococcygeal Teratomas Bülent Özçelik, Mustafa Baþbuð, Ý. Serdar Serin, Mehmet Tayyar, Kayseri-Turkey ... Esra Aktepe Keskin, Ahmet C. Çalýþkan, Nuri Danýþman, Ankara-Turkey Reproductive Endocrinology and Infertility Influences of Uterine Tubal Factors on Oocyte Maturation and Embryo Segmentation Firdevs Gürer, Varol Þahintürk, Cengiz Bayçu, A. Ergin Açýkalýn, Eskiþehir-Turkey Unicornuate Uterus: Analysis of 55 Cases Didem Bayar, Dilek Uygur, Banu Yüksel, Münire Erman Akar, A. Seval Erdinç, Tuncay Küçüközkan, Ankara-Turkey Gynecology and Gynecological Oncology Contraceptive Awareness in Manisa Region Yýldýz Uyar, Ümit Sungurtekin Ýnceboz, H. Tayfun Özçakýr, Yeþim Bülbül Baytur, Manisa-Turkey Can Femoral Neck Length and Width be A Predictor for Osteoporosis? Murat Api, Gültekin Köse, Nurettin Aka, Özgür Kartal, Ýstanbul-Turkey Case Report Primary Carcinoma of the Fallopian Tube: The Rarest Gynecologic Malignancy: (Report of Five Cases) Tayfun Güngör, H. Levent Keskin, Sema Zergeroðlu, Esra A. Keskin, Hakan Yalçýn, Tuðrul Aydoðdu,

29. EMedicine - Meckel-Gruber Syndrome : Article By Suzanne M Carter, MS Synonyms and related keywords MKS, dysencephalia splanchnocystica, Grubersyndrome, Gruber s syndrome, Meckel syndrome type 1, MKS1, MES. http://www.emedicine.com/ped/topic1390.htm

(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease Meckel-Gruber Syndrome Last Updated: May 19, 2003 Rate this Article Email to a Colleague Synonyms and related keywords: MKS, dysencephalia splanchnocystica, Gruber syndrome, Gruber's syndrome, Meckel syndrome type 1, MKS1, MES AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Suzanne M Carter, MS , Senior Genetic Counselor, Associate, Department of Obstetrics and Gynecology, Division of Reproductive Genetics, Montefiore Medical Center, Albert Einstein College of Medicine Coauthor(s): Susan J Gross, MD, FRCS(C), FACOG, FACMG , Codirector, Division of Reproduction Genetics, Associate Professor, Department of Obstetrics and Gynecology, Albert Einstein College of Medicine Suzanne M Carter, MS, is a member of the following medical societies: American College of Medical Genetics Editor(s): Christian J Renner, MD

30. EMedicine - Meckel-Gruber Syndrome : Article Excerpt By: Suzanne M Carter, MS Synonyms, Key Words, and Related Terms MKS, dysencephalia splanchnocystica,Gruber syndrome, Gruber s syndrome, Meckel syndrome type 1, MKS1, MES. http://www.emedicine.com/ped/byname/meckel-gruber-syndrome.htm

(advertisement) Excerpt from Meckel-Gruber Syndrome Synonyms, Key Words, and Related Terms: MKS, dysencephalia splanchnocystica, Gruber syndrome, Gruber's syndrome, Meckel syndrome type 1, MKS1, MES Please click here to view the full topic text: Meckel-Gruber Syndrome Background: Meckel-Gruber syndrome (MKS) (OMIM 24900) is a lethal, rare autosomal recessive condition mapped to chromosome 17. The triad of occipital encephalocele, large polycystic kidneys, and postaxial polydactyly characterizes MKS. Associated abnormalities include oral clefting, genital anomalies, CNS malformations, and fibrosis of the liver. Pulmonary hypoplasia is the leading cause of death. With the advent of ultrasonography, prenatal diagnosis is possible during the second trimester or late first trimester. Pathophysiology: It has been suggested that a failure of mesodermal induction causes MKS. The induction cascades of early morphogenesis involve numerous growth factors, homeo box genes, and paired domain genes. Frequency: Internationally: Worldwide, incidence of MKS varies from 1 in 13,250 to 1 in 140,000 live births. There is a predilection for the Finnish population, in whom the birth incidence is 1 in 9000.

31. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/D Syndrome@ (4); Dubowitz Syndrome@ (4); Dwarfism@ (11); dysencephalia splanchnocystica@(4); DyslexiaDysgraphia-Dyscalculia@ (15); Dysmenorrhea http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/D

Match: sort by: relevance date Free Services Subscribe by email RSS newsfeeds PDA-friendly format loc="/images/" A A A Find Jobs In: Healthcare Engineering Accounting College Contract / Freelance Customer Service Diversity Engineering Executive Healthcare Hospitality Human Resources Information Tech International Manufacturing Nonprofit Retail All Jobs by Job Type All Jobs by Industry Relocating? Visit: Moving Resources Moving Companies Mortgage Information Mortgage Calculator Real Estate Lookup Front Page Today's Digest Week in Review Email Updates ... Conditions and Diseases D (0 links) DES Syndrome Dandy Walker Syndrome De Lange Syndrome Deafblindness ... Dystonia Musculorum Deformans News about D [ More news about D Books about D List Price: Amazon.com's Price: You Save: Prices subject to change. The Feeling Good Handbook by: David D. Burns December, 1999 List Price: Amazon.com's Price: You Save: Prices subject to change. The Double Helix : A Personal Account of the Discovery of the Structure of DNA by: James D. Watson 12 June, 2001 List Price: Amazon.com's Price: You Save: Prices subject to change.

32. 1684 29, 1684. The description is suggestive of a diagnosis of MeckelGrubersyndrome (dysencephalia splanchnocystica). This may represent http://mind-brain.com/abstracts.php?qa=1684

33. Meckel-Gruber Syndrome Information Diseases Database MeckelGruber syndrome,dysencephalia splanchnocystica, Disease Database Information. Meckel-Grubersyndrome aka/or dysencephalia splanchnocystica http://www.diseasesdatabase.com/ddb31661.htm

Diseases Database Index Sponsors Contact ... Previous Page Meckel-Gruber syndrome Information Search 2 synonyms or equivalents were found. Meckel-Gruber syndrome aka/or Dysencephalia splanchnocystica may cause or feature (Follow link for list) may be associated with (Follow link for list) belong(s) to the category of (Follow link for list) No UMLS definitions Meckel-Gruber syndrome: specific sites Send Meckel-Gruber syndrome to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation i-medicine.info - the evidence based medicine, informatics and audit portal Valid XHTML 1.0 Served 2004-06-02 11:55:27 Metadata Updated 2004-05-22

34. Disease, Medication, Symptom Etc Database Index : D Diseases Database Reticulate acropigmentation of Dohi Dyschromatosis universalis hereditaria Dyschromiasee Skin discoloration dysencephalia splanchnocystica see MeckelGruber http://www.diseasesdatabase.com/disease_index_d.asp

Diseases Database Index Sponsors Contact ... Previous Page Disease, medication, symptom etc database index : D Search see Stavudine Dacarbazine Daclizumab Dacrocystitis see Dacryocystitis Dacrocytosis see Teardrop poikilocytes Dacryoadenitis Dacryocystitis Dacryocytes see Teardrop poikilocytes Dactinomycin see Actinomycin D Dactylitis Dactylolysis spontanea see Ainhum Dactylysis spontanea see Ainhum Dalmatian hypouricemia Dalteparin Danaparoid sodium ... Danazol Dancing eyes-dancing feet syndrome see Opsoclonus myoclonus syndrome Dandruff see Seborrhoeic dermatitis Dandy-Walker syndrome Danielssen-Boeck disease see Lepromatous leprosy Danon disease see Glycogenosis type 2b Danthron see Dantron Dantrolene Dantron Dapiprazole Dappled metaphysis syndrome see Strudwick spondylometaepiphyseal dysplasia Dapsone Daptomycin Darbepoetin alfa see Erythropoietin Darier's disease see Keratosis follicularis (congenital) Darier's sign Darier-White disease see Keratosis follicularis (congenital) Darifenacin Daunorubicin Davidson disease see Congenital microvillous atrophy Dazoxiben DDAVP see Antidiuretic hormone DDC see Zalcitabine DDI see Didanosine De Clerambault's syndrome see Kandinsky syndrome de Grouchy syndrome type 1 see Deletion of short arm of chromosome 18 de Grouchy syndrome type 2 see Deletion of long arm of chromosome 18 De la Chapelle dysplasia De Lange syndrome see Cornelia de Lange syndrome de Morsier syndrome see Septo-optic dysplasia de Morsier-Gauthier syndrome see Kallmann syndrome De Quervain's tenosynovitis De Quervain's thyroiditis De Sanctis-Cacchione syndrome see Xeroderma pigmentosum group D de Vaal disease

35. Healthwise Synonyms. dysencephalia splanchnocystica; Gruber Syndrome; MeckelGruberSyndrome; MES; MKS. Disorder Subdivisions. None. General Discussion. http://www.stlukes-sf.sutterhealth.org/health/healthinfo/index.cfm?section=healt

36. Heilpflanzen-Welt - Die Welt Der Heilpflanzen! Translate this page dysencephalia. dysencephalia splanchnocystica Gruber’s syndrome, Meckel’s syndrome,Meckel-Gruber syndrome. Homepage Gesundheit (gesund, schlank, fit). http://04.nx8.de/2959.htm

37. TheFetus.net - Meckel Syndrome -Sandra R Silva, MD & Philippe Jeanty, MD, PhD Synonyms dysencephalia splanchnocystica, Meckel syndrome (used inEnglish literature). This is the preferred appellation and is http://www.thefetus.net/page.php?id=427

38. Search By Disease 127 Dyschondrosteosis (DCO). 128 dysencephalia splanchnocystica. 129 Dyserythropoieticanemia, congenital, type II. 130 Dyserythropoietic anemia, hempas type. http://www.eddnal.com/directory/disease.php?letter=D&page=9

39. Article : Antenatal Ultrasound Diagnosis Of Meckel-Gruber Syndrome ; Author : N Discussion Meckel –Gruber syndrome is also known as dysencephalia splanchnocysticaMeckel syndrome (used in English literature) and Gruber syndrome (used in http://www.ijri.org/articles/archives/20011104/case.htm

Antenatal Ultrasound Diagnosis of Meckel-Gruber Syndrome N Dahiya, Vijay S, S Prabhakar, S Subramaniam, Neha Dahiya Ind J Radiol Imag 2001 11:4:199-201 Keywords: Beckwith-Wiedmann syndrome, adrenal gland, cysts Introduction Meckel-Gruber syndrome is a rare and lethal autosomal recessive disorder characterized by occipital encephalocele, postaxial polydactyly and bilateral dysplastic cystic kidneys. It can be associated with many other conditions. Antenatal ultrasound examination can establish the correct diagnosis by identifying at least two of the major features described. Material and Methods A twenty-five-year-old woman with 16 weeks amenorrhea was referred for a second trimester ultrasonogram to detect fetal anomalies. There was history of first-degree consanguinity. The patient had two previous second trimester abortions. Records were not available and the patient stated that both the abortions were due to “abnormal kidneys”. Ultrasonography was done using GE logiq 500 PRO equipment, with a 4MHz Curvilinear transducer. The scan revealed bilateral enlarged hyperechoic kidneys (Fig.1,2), occipital encephalocele (Fig.3), six digits in all four limbs (Fig.4) and bilateral clubfeet. Though there was no oligohydramnios the fetal urinary bladder was not visualised both in the initial scan and in all repeat scans done over a period of two days.

40. Pathology Cases For Diagnosis but wellstudied disorder. It is also known as Meckel-Gruber Syndrome(dysencephalia splanchnocystica). It is transmitted through http://www.usuhs.mil/pat/surg_path/s98-01/98-01.html

Case 98-01: Pediatric Syndromes I Contributed by: R. L. Katz, LCDR, MC, USNR Objectives: 1. Discuss clinical presentation, clinical course, inheritance pattern for Meckel Syndrome. 2. Discuss the diagnostic features of Meckel Syndrome including those listed as "minimal diagnostic criteria." 3. List the different diagnostic considerations for Meckel Syndrome. History: A 20-year-old gravida one para female at 39 weeks estimated gestational age presented to Labor and Delivery with spontaneous rupture of membranes with baby in breech position. A primary, low transverse C-section was performed with birth of a liveborn infant female. Apgar scores at one minute were one, five minutes one, and ten minutes four, with difficult ventilation (inadequate oxygenation despite maximal ventilatory settings). Multiple congenital anomalies were noted at birth. Ventilatory support was discontinued and the infant expired at approximately five hours of life. Permission for a full autopsy was granted by the infant's parents. Illustrations Figure 1 Posterior view of head showing occipital encephalocele and microcephaly Figure 2 Ear anomalies.

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