81. D - E http//www.tri21.org. dubowitz syndrome. See also Craniofacial Disorders; GrowthDisorders. dubowitz syndrome Parent Support Network. http//dubowitz.org. http://1stnetwork.tripod.com/resources/id16.html

Get Five DVDs for $.49 each. Join now. Tell me when this page is updated First Network's National Resources D - E Home A B C D - E F G H I - J - K ... T - U - V - W - X If the information you were looking for isn't found here, email First Network Online for additional assistance. Click here to send an email and request additional assistance. DANDY-WALKER SYNDROME See also: Hydrocephalus Dandy Walker Home Page http://www.geocities.com/Heartland/Hills/3919/dws.html NINDS Dandy Walker Syndrome Information Page http://www.ninds.nih.gov/health_and_medical/disorders/dandywalker.htm DARIER DISEASE See: Ichthyosis DE BARSEY SYNDROME DE BARSEY-MOENS-DIERCKS SYNDROME See: Connective Tissue Disorders DEAF-BLIND See also: Hearing Impairments; Visual Impairments Deaf Blind Resources http://dww.deafworldweb.org/int/us/deafblind.html National Family Association for Deaf-Blind http://www.NFAD.org DEAFNESS See: Hearing Impairments DIABETES INSIPIDUS See also: Autoimmune Disorders The Diabetes Insipidus Foundation, Inc. http://diabetesinsipidus.maxinter.net DIABETES MELLITUS See also: Autoimmune Disorders; Kidney Disorders

82. Links: Health: Rare Disorders- Alabama Council For Developmental Disabilities Vomiting Syndrome; Cystinosis; Dandy Walker Syndrome; Degos; DercumDisease; DiGeorge Syndrome; dubowitz syndrome; Dystonia; EhlersDanlos http://www.acdd.org/Links/conditions/Rare_Disorders.htm

You are here: Home Links Conditions Rare Disorders Rare Disorders Home About Definition Planning ... Search 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.

83. Electricbrain Home: Index: Health: Conditions And Diseases: Genetic Disorders LaurenceMoon Syndrome Mannosidosis Zellweger Syndrome Weaver Syndrome WaardenburgSyndrome Ectodermal Dysplasia Costello Syndrome dubowitz syndrome Velo-Cardio http://www.electricbrain.com/index/Health/Conditions_and_Diseases/Genetic_Disord

electricbrain Index Health Conditions and Diseases : Genetic Disorders home index write privacy ... Noonan Syndrome Famous quotes: I have never seen anything fill up a vacuum so fast and still suck. Rob Pike, on X. Steve Jobs said two years ago that X is brain-damaged and it will be gone in two years. He was half right. Dennis Ritchie Dennis Ritchie is twice as bright as Steve Jobs, and only half wrong. Jim Gettys Find someone: Old Friends New Friends Lost Love New Love ... privacy

84. Dolphin Aid syndrome; Depression; Development delay; Diplegia; Down Syndrome; DPTdamage; Drash syndrome; dubowitz syndrome; Duchennes musc. Dystrophy; http://www.dolphin-aid.de/main02_4.htm

A : Agnesis of corpus callosum Angelman syndrome Anoxia Aphasia Apoplexy Ataxia Ataxia telangiectasia Attention deficit disorder Auditory processing disorder Autism B : Bacterial meningitis Behaviour disorder Brain tumor Bronchio-pulmonary disease C : Canavan leukodystrophy Cander Cerebral atrophy Cerebral diplegia Cerebral hyperplasia Cerebral palsy Chromosome anomaly Coffin-sirrus sindrome Cornelia de Lange syndrome Costello syndrome Cri-du-chat Cystic fibrosis Cytomegalyvirus D : Dandy-Walkers syndrome Degenerative muscle syndrome DeGeorge syndrome Depression Development delay Diplegia Down Syndrome DPT damage Drash syndrome Dubowitz syndrome Duchennes musc. Dystrophy Dysarthria Dyslexia Dysphasia Dyspraxia Dystonia E : Elective mutism Encephalitits Encephalopathy Epilepsy Ewing's sarcoma F : Fragile X syndrome Freidrich's ataxia H : Hearing disorder Heart defect Hemangioma Hemipegia Hidden infantile spasms Hodgkins Holoprosencephaly Hurler syndrome Hydrocephaly Hydrocephaly-achondr. Hydroencephalitis Hypotonia Hypoxia I : Infantile spasms Inflammation of the brain J: Joubert syndrome Juvenile encephalitits K : Kabuki syndrome L : Landau-Kleffner syndr.

85. WebRing: Hub flamingoland (becca has dubowitz syndrome, pic on page) flamingoland is our homepageand becca is our youngest, she has dubowitz syndrome, which is an orphan http://p.webring.com/hub?ring=spneed&list&page=3

86. Health Library Duane Syndrome. Dubin Johnson Syndrome. dubowitz syndrome. Duhring Disease.Duodenal Atresia or Stenosis. Dupuytren's ContractureDupuytren's Disease. http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/_SearchResults.

87. CRGM - D1a Translate this page www.familyvillage.wisc.edu/lib_aars.htm. dubowitz syndrome Informationand Parent Support, www.dubowitz.org/. Tourette Syndrome Faq, http://www.crgm.qc.ca/d1a.html

Documentation : Liens vers d'autres sites Déficience intellectuelle Association américaine du retard mental www.aamr.org/ L'AAMR-QUEBEC est le chapitre québécois de l'American Association on Mental www.er.uqam.ca/nobel/r17630/aamr_qc.html www.total.net/~aqisiqdi/ www.delegation.ca/amdi www.aoihi.qc.ca/ w.aoihi.qc.ca/ Service de réadaptation L'Intégrale www.integrale.org/ CRDI Chaudière-Appalaches www.quebec-affaires.com/crdi _dyna/default.lasso Réseau de services en défience intellectuelle (outaouais) www.rsdi.qc.ca/index.html Centres Butters-Savoy et Horizon www.cbsh.qc.ca/ http://pages.citenet.net/users/ ctq162/rrppadim/menu/rrppadim.html Gouvernement s Gouvernement du Canada Conseil de recherches en sciences humaines du Canada www.sshrc.ca/ Info centre du gouvernement du Canada http://canada.gc.ca/main_f.html www.gouv.qc.ca/ www.ophq.gouv.qc.ca/ www.trpocb.cam.org/ Rapport de la commission Clair «Solutions émergentes » http://www.cessss.gouv.qc.ca/ pdf/fr/00-109.pdf www.rrsss06.gouv.qc.ca/ Autisme www.autisme.qc.ca/

88. Dubowitz (syndrome De) Translate this page dubowitz (syndrome de). voir également croissance, microcéphalie, rétrognatisme,hypertélorisme. Affection héréditaire à transmission http://www.vulgaris-medical.com/textd/dubowitz.htm

Dubowitz (syndrome de) Agitation Le squelette Agrandissement de la base du nez, qui a une forme pointue et est plus petite que la moyenne 3) La peau Biblio

89. Service Page - Pathologie Information Translate this page MALADIE dubowitz, syndrome de, CIM Q87.13, Le syndrome de dubowitza été rapporté pour la première fois en 1965. Il est http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=235

90. Cancer Prone Diseases Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma (DMSMFH). Dubowitzsyndrome. Dyskeratosis congenita (DKC). Dysplastic nevus syndrome (DNS). http://www.infobiogen.fr/services/chromcancer/Kprones/Kproneliste.html

Atlas of Genetics and Cytogenetics in Oncology and Haematology Home Genes Leukemias Solid Tumours ... NA Cancer Prone diseases Ataxia telangiectasia Bannayan-Riley-Ruvalcaba syndrome Beckwith-Wiedemann syndrome Bloom syndrome ... Teaching

91. Genetic Disorders : Meddie Health Search Cystic Fibrosis (63). DiGeorge syndrome (5). Down syndrome (64). Dubowitzsyndrome (5). Ectodermal Dysplasia (5). Familial Hypercholesterolemia (6). http://www.meddie.com/search/Health/Conditions_and_Diseases/Genetic_Disorders/

HOME ADD A LINK MODIFY A LINK NEW LINKS ... TOP RATED Search Meddie: the entire directory only this category More search options Home Health Conditions and Diseases : Genetic Disorders CATEGORIES: Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome Alagille Syndrome ... Zellweger Syndrome ITEMS: LINKS: Acid Maltase Deficiency A brief summary of AMD along with links and news. (Rating: 0.00 Votes: 0) Rate It Chromosome Deletion Outreach. Provides support and information to families. Includes family stories, a library, FAQs and resources. (Rating: 0.00 Votes: 0) Rate It Dr. Greene's HouseCalls A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. (Rating: 0.00 Votes: 0) Rate It GeneClinics: Medical Genetics Knowledge Base NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients. (Rating: 0.00 Votes: 0) Rate It Genetic and Rare Conditions Site Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z. (Rating: 0.00 Votes: 0)

92. Dubowitzin Oireyhtymä Kehitysvammahuollon tietopankki. Intrauterine dwarfism (kohdunsisäinenkääpiökasvuisuus). Dubowitzin oireyhtymä. Dubowitzin oireyhtymä http://www.saunalahti.fi/kup/syndroma/dubowitz.htm

Kehitysvammahuollon tietopankki Intrauterine dwarfism (kohdunsisäinen kääpiökasvuisuus) Dubowitzin oireyhtymä Dubowitzin oireyhtymä on hyvin harvinainen sairaus (vuosittain syntyy koko maailmassa n. 40 lasta), jota luonnehtii kasvun hidastuminen, lyhytkokoisuus ja poikkeavat kasvonpiirteet. Oireet voivat ilmaantua jo sikiövaiheessa tai heti syntymän jälkeen. Sairastuneista puolet kehitysvammaisia Noin puolet oireyhtymään sairastuneista on kehitysvammaisia. Henkinen jälkeenjääneisyys on useimmiten lievää Dubowitzin oireyhtymän erikoispiirteitä ovat pienipäisyys, kallon saumojen ennenaikainen luutuminen, korkea otsa ja leveä nenänselkä, poikkeavat silmäkuopat, etäällä toisistaan olevat silmät ( hypertelorismi ) ja riippuluomet sekä luomirakojen ahtaus. Niinikään kasvojen, polvien ja kyynärpäiden syyhyävät punaiset ihoalueet ovat tavanomaisia. Ääni on erikoisen korkea tai käheä. Leuka on usein pienikokoinen ja nielu vajaakehittynyt. Epämuodostumia ja poikkeuksellista tulehdusalttiutta Muina oireina esiintyy mm. piilokiveksisyyttä, siittimen alahalkioita, valtimoiden poikkeavuuksia, peräaukon epämuodostumista ja lisäkilpirauhasen vajaatoimintaa. Lisäksi infektioalttius, uusiutuvat haavaiset suutulehdukset, lisääntynyt kasvainriski ja luuytimen vaurioituminen sekä valkosolujen niukkuus ovat osa taudinkuvaa.

93. Mioti: Medical Condition Dry Eyes, • Dry Skin. • Duane syndrome, • Dubin Johnson syndrome. • Dubowitzsyndrome, • Duchennes Paralysis. • Duhring Disease, • Duodenal Atresia. http://www.mioti.com/cat/condition/results.asp?Alpha=D

94. Katalog - Wirtualna Polska Serwis Katalog w Wirtualna Polska S.A. pierwszy portal w Polsce. http://katalog.wp.pl/DMOZ/Health/Conditions_and_Diseases/Genetic_Disorders/Dubow

Poczta Czat SMS Pomoc Szukaj.wp.pl: -Katalog -Polskie www -¦wiatowe www -Wirtualna Polska -FTP/Pliki -Grupy dyskusyjne -Encyklopedia -Produkty wp.pl Katalog Katalog ¦wiatowy DMOZ ... Conditions and Diseases > Genetic Disorders Fakty o Katalogu Pomoc Regulamin Serwis szukaj ... Ostatnio dodane NAWIGACJA Fakty o katalogu Pomoc Regulamin Serwis Szukaj ... FAQ Dodaj stronê Katalog WP Polskie Strony WWW Oferta dla firm WP-HIT ... Wirtualna Polska

95. Casi Clinici - Novembre 2000 Translate this page skin eruption. J Med Genet, 2, 12, 1965 2) Ilyina HG, Lurie IW Dubowitzsyndrome possible evidnece for a clinical subtype . Am J http://www.medicoebambino.com/elettroniche/archivio/ARCH2000/CL/CL11000.htm

P.E. Contributi originali - Casi clinici - Novembre 2000 CASI CLINICI Sindrome di Dubowitz con reflusso vescico-ureterale e agenesia renale. Confronto con le sindromi da instabilità cromosomica Borrelli A, Festa R UO Pediatria, Azienda Ospealiera Moscati, Avellino Descrizione di un caso di sindrome di Dubowitz (ipostaturalità, microcefalia, iperattività, lieve deficit di intelligenza, fisionomia sui generis, capelli radi, ptosi palpebrale) associata a agenesia renale. Il caso viene confrontato con altre sindromi genetiche, in ispecie con la sindrome di Bloom e con la sindrome di Nijmegen, tutte caratterizzate, come la Atassia-Teleangectasia e la sindrome di Fanconi, da fragilità cromosomica. Il caso Arriva alla nostra osservazione, per diarrea protratta, all'età di 7 anni, una bambina con una sindrome dismorfica caratterizzata da bassa statura (116 cm= 5°centile) e basso peso (22Kg=10° centile), microcefalia (cc cm 46,5cm), ritardo psicomotorio lieve, con iperattività, eczema agli arti, capelli radi. L'esame dimorfologico dimostra:  fronte sfuggente, ptosi palpebrale SN, mento appuntito, mandibola ipoplasica, impianto basso delle orecchie. Gli esami generali sono tutti negativi. L'insieme viene inquadrato come sinrome di Dubowitz La bambina non è al suo primo ricovero: in precedenza, era già stata visitata per convulsioni febbrili, all'età di un anno, e poi, a 6 anni, per disturbi minzionali, correlati ad una infezione urinaria. In quelle occasioni, accanto ai segni del ritardo mentale, dell'iperattività, dell'eczema e della microcefalia, che avevano suggerito una patologia sindromica, peraltro non ancora definita,  era stata constatata una agenesia del rene dx e un reflusso di III grado a sinistra (ecografia, scintigrafia, cistouretrografia minzionale)

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