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         Dysencephalia Splanchnocystica:     more detail

1. Meckel Syndrome
dysencephalia splanchnocystica; Gruber Syndrome; MeckelGruber Syndrome; MES;MKS. Disorder Subdivisions. Meckel Syndrome Type 1; Meckel Syndrome Type 2
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Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Meckel Syndrome Important It is possible that the main title of the report Meckel Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms
  • Dysencephalia Splanchnocystica Gruber Syndrome Meckel-Gruber Syndrome MES MKS
Disorder Subdivisions
  • Meckel Syndrome Type 1 Meckel Syndrome Type 2 Meckel Syndrome Type 3
General Discussion Meckel syndrome is a rare inherited disorder characterized by abnormalities affecting several organ systems of the body (multisystem). Three classic symptoms are normally associated with Meckel syndrome: protrusion of a portion of the brain and its surrounding membranes (meninges) through a defect in the back or front of the skull (occipital encephalocele), multiple cysts on the kidneys (polycystic kidneys), and extra fingers and/or toes (polydactyly). Affected children may also have abnormalities affecting the head and face (craniofacial area), liver, lungs, and genitourinary tract. Meckel syndrome is inherited as an autosomal recessive trait. Resources Genetic Alliance 4301 Connecticut Avenue NW Suite 404 Washington, DC 20008-2304

2. MECKEL-GRUBER SYNDROME (DYSENCEPHALIA SPLANCHNOCYSTICA)
Features Listed For MECKELGRUBER SYNDROME (dysencephalia splanchnocystica) McKusick 249000. Abnormal liver (including function)
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3. Index
dysencephalia splanchnocystica Dysfunctional Uterine Bleeding DysgammaglobulinemiaType I Dyskeratosis Congenita Dyskeratosis Congenita Syndrome
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Who We Are About WebMD Site Map You are in Medical Library Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... Support Organizations Search the Help Health Topics Click a letter to see a list of topics beginning with that letter A B C D ... DY D D Trisomy Syndrome back to top DA Da Costa's Syndrome Dacryosialoadenopathia Dacryosialoadenopathy Dalpro, Fetal Effects From ... back to top DB DBA DBS back to top DD DD back to top DE De Barsy Syndrome De Barsy-Moens-Diercks Syndrome de Lange Syndrome De Morsier Syndrome ... back to top DG DGS DGSX Golabi-Rosen Syndrome, Included back to top DH DH DHOF back to top DI Diabetes in Pregnancy (Gestational Diabetes) Diabetes Insipidus Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness Diabetes Insipidus, Neurohypophyseal ... back to top DJ DJS back to top DK DKC back to top DL DLPIII back to top DM DM DMC Disease DMC Syndrome DMD ... back to top DN DNS, Hereditary

4. Webkatalog
2. Human Genome Mapping Project A list of features for meckel-gruber syndrome, also known as dysencephalia splanchocystica.
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5. Dysencephalia Splanchnocystica - Definition Of Dysencephalia Splanchnocystica In
Definition of dysencephalia splanchnocystica in the Medical Dictionary and Thesaurus.dysencephalia splanchnocystica explanation.
http://medical-dictionary.thefreedictionary.com/dysencephalia splanchnocystica
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dysencephalia splanchnocystica
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Cite / link Email Feedback dys·en·ce·pha·li·a splanch·no·cys·ti·ca (d s- n s -f l spl ngk n -s s t -k , -f l y n. See Meckel syndrome Mentioned in No references found Medical browser Full browser dyschondroplasia dyschondrosteosis dyschromatopsia dyschromia ... dysembryoma dysencephalia splanchnocystica dysentery dyserethism dysergia dysesthesia ... Dysembryoplastic Neuroepithelial Tumor dysencephalia splanchnocystica Dysentary Dysentary Dysentary Dysentary ... Dysfunction (album) Word (phrase): Word Starts with Ends with Definition Free Tools: For surfers: Browser extension Word of the Day NEW! Help For webmasters: Free content NEW!

6. Genetics Of The Meckel Syndrome (dysencephalia Splanchnocystica)
Genetics of the meckel syndrome (dysencephalia splanchnocystica)
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7. Dyscheiria - Definition Of Dyscheiria In The Medical Dictionary - By The Free On
Dysderidae DYSEAC dysembryoma Dysembryoplastic Neuroectodermal Tumor Dysembryoplastic Neuroepithelial Tumor dysencephalia splanchnocystica
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dyscheiria
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Cite / link Email Feedback dys·chei·ri·a or dys·chi·ri·a (d s-k r n. The inability to recognize which side of the body has been touched even though there is no apparent loss of sensation. dys·chei ral adj. Mentioned in syncheiria Medical browser Full browser dysarthrosis dysautonomia dysbarism dysbasia ... dyscephalia dyscheiria dyschezia dyschondrogenesis dyschondroplasia dyschondrosteosis ... dyscephalia dyscheiria dyschezia dyschezia dyschondrogenesis dyschondroplasia ... Dysentary Word (phrase): Word Starts with Ends with Definition Free Tools: For surfers: Browser extension Word of the Day NEW! Help For webmasters: Free content NEW!

8. Dysencephalia Splanchnocystica
Web resources on dysencephalia splanchnocystica.
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9. Meckel Syndrome
Synonyms. dysencephalia splanchnocystica; Gruber Syndrome; MeckelGruber Syndrome;MES; MKS. Disorder Subdivisions. Meckel Syndrome Type 1; Meckel Syndrome
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National Organization for Rare Disorders, Inc.
Meckel Syndrome
Important
It is possible that the main title of the report Meckel Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
  • Dysencephalia Splanchnocystica Gruber Syndrome Meckel-Gruber Syndrome MES MKS
Disorder Subdivisions
  • Meckel Syndrome Type 1 Meckel Syndrome Type 2 Meckel Syndrome Type 3
General Discussion
Meckel syndrome is a rare inherited disorder characterized by abnormalities affecting several organ systems of the body (multisystem). Three classic symptoms are normally associated with Meckel syndrome: protrusion of a portion of the brain and its surrounding membranes (meninges) through a defect in the back or front of the skull (occipital encephalocele), multiple cysts on the kidneys (polycystic kidneys), and extra fingers and/or toes (polydactyly). Affected children may also have abnormalities affecting the head and face (craniofacial area), liver, lungs, and genitourinary tract. Meckel syndrome is inherited as an autosomal recessive trait.
Resources
Genetic Alliance
4301 Connecticut Avenue NW
Suite 404
Washington, DC 20008-2304

10. Meckel Syndrome Dysencephalia Splanchnocystica Gruber
Meckel Syndrome dysencephalia splanchnocystica Gruber Syndrome MeckelGruber Syndrome MES MKS Meckel Syndrome dysencephalia splanchnocystica Gruber
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11. Medizin-Lexikon - Diagnose Dysencephalia Splanchnocystica ICD Q61.9
Medizin ICD 10 dysencephalia splanchnocystica Q61.9
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12. Case Of The Month September 1998
Miszbildungen (Akrocephalosyndactylie und dysencephalia splanchnocystica) Beitr . Howe JJ (1969) The Meckel Syndrome (dysencephalia splanchnocystica,
http://www.obgyn.net/us/cotm/9809/cotm_9809.htm
OBGYN.net Ultrasound: Case of the Month Sept. 1998 The Meckel Syndrome by Hans van der Slikke, MD
1. In 1992 a 27 year old woman was seen in our obstetric ultrasound department, because of routine sonography for her first pregnancy of 16 weeks and 4 days. Her general history were negative, as was her family history. The ultrasound showed dilated ventricles and an occipital encephalocele. Both kidneys showed multiple cysts (picture 1.) Diagnosis: Meckel-Gruber syndrome. A few days later her pregnancy was terminated with a sulproston infusion. Pathology confirmed the diagnosis. Next to the already described malformations the right foot counted 6 toes, while the left hand showed an extra finger. Because the Meckel-Gruber syndrome is a recessive disease, she was told that she had a 25% chance of having an affected fetus in her next pregnancy. 2. Five months later she reported a new pregnancy. At 9 weeks she seemed to have a normal ultrasound, but at 12 weeks a cranial cyst was seen (picture 2.). Pathology: because of the curettage it was difficult to recognize fetal parts. However two hands with 6 fingers each were found. This seems a confirmation of the diagnosis M-G syndrome.

13. Dorlands Medical Dictionary
dysencephalia splanchnocystica (dys en ce pha lia splanch no cys ti ca) (disen sschwa-fa le-schwa splank no-sis t
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14. Genetics Of The Meckel Syndrome (dysencephalia Splanchnocystica) -- Hsia Et Al.
Genetics of the meckel syndrome (dysencephalia splanchnocystica). YE Hsia, MBratu and A Herbordt Division of Medical Genetics, Departments of Medicine and
http://pediatrics.aappublications.org/cgi/content/abstract/48/2/237
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This Article P Rs: Submit a response Alert me when this article is cited Alert me when P ... Alert me if a correction is posted Services E-mail this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Hsia, Y. E. Articles by Herbordt, A. Pediatrics, Aug 1971, 237-247, Vol 48, No. 2
Genetics of the meckel syndrome (dysencephalia splanchnocystica)
YE Hsia, M Bratu and A Herbordt
Division of Medical Genetics, Departments of Medicine and Pediatrics, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06510. ABSTRACT. Seven cases in two families are reported of the Meckel syndrome; two sets of male identical twins in one family, and three affected siblings in another. The key features of this syndrome are occipital encephalocele, cleft lip and palate, polydactyly, and polycystic kidneys. Additional malformations frequently found include microcephaly, micrognathia, absence

15. EMedicine - Meckel-Gruber Syndrome Article By Suzanne M Carter, MS
Synonyms and related keywords MKS, dysencephalia splanchnocystica, Gruber syndrome, Gruber's syndrome, Meckel syndrome type 1, MKS1, MES
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16. Meckel-Gruber Syndrome Information Diseases Database
MeckelGruber syndrome dysencephalia splanchnocystica, Disease Database Information
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17. Entrez PubMed
Meckel syndrome (Gruber syndrome, dysencephalia splanchnocystica). KaganHallet K.Publication Types. Case Reports. MeSH Terms
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=4

18. Entrez PubMed
Mil Med. 1977 Oct;142(10)772, 780. Case for diagnosis. Meckel syndrome (Grubersyndrome, dysencephalia splanchnocystica). KaganHallet K. Publication Types
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=4

19. Index - Trustworthy, Physician-Reviewed Information From WebMD
with Hemangiomas Dyschondroplasia Dyschondrosteosis Dyschromatosis UniversalisHereditaria dysencephalia splanchnocystica Dysfunctional Uterine Bleeding
http://content.health.msn.com/hw/index/index-topics-D.asp

20. Meckel Syndrome
covered by this report. Synonyms. dysencephalia splanchnocystica; Gruber Syndrome;MeckelGruber Syndrome; MES; MKS. Disorder Subdivisions.
http://www.peacehealth.org/kbase/nord/nord661.htm
var hwPrint=1;var hwDocHWID="nord661";var hwDocTitle="Meckel Syndrome";var hwRank="1";var hwSectionHWID="nord661-Header";var hwSource="en-usQ3_05";var hwDocType="Nord";
National Organization for Rare Disorders, Inc.
Meckel Syndrome
Important
It is possible that the main title of the report Meckel Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
  • Dysencephalia Splanchnocystica Gruber Syndrome Meckel-Gruber Syndrome MES MKS
Disorder Subdivisions
  • Meckel Syndrome Type 1 Meckel Syndrome Type 2 Meckel Syndrome Type 3
General Discussion
Meckel syndrome is a rare inherited disorder characterized by abnormalities affecting several organ systems of the body (multisystem). Three classic symptoms are normally associated with Meckel syndrome: protrusion of a portion of the brain and its surrounding membranes (meninges) through a defect in the back or front of the skull (occipital encephalocele), multiple cysts on the kidneys (polycystic kidneys), and extra fingers and/or toes (polydactyly). Affected children may also have abnormalities affecting the head and face (craniofacial area), liver, lungs, and genitourinary tract. Meckel syndrome is inherited as an autosomal recessive trait.
Resources
Genetic Alliance
4301 Connecticut Avenue NW
Suite 404
Washington, DC 20008-2304

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