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
Extractions: 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. 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 See: Ichthyosis See: Connective Tissue Disorders 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 See: Hearing Impairments See also: Autoimmune Disorders The Diabetes Insipidus Foundation, Inc. http://diabetesinsipidus.maxinter.net See also: Autoimmune Disorders; Kidney Disorders
Extractions: On this page: 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.
Extractions: 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
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
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
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.
Extractions: 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/
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
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
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
Extractions: 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. 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. 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.
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
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
Extractions: 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)
