PHP : Resource Details dubowitz syndrome Parent Support Network WEHRAHM. Address, 23 E. Dawes AvenueSomers Point, NJ 08244-2714 MapQuest. Phone, 609-823-1206 http://www.php.com/include/agency/agency_item.php?AgencyID=775&where_keywords=
Centre For Genetics Education:: Disorder Information And Support Drash Syndrome Duane Syndrome dubowitz syndrome Dupuytren Contraction DyschondrosteosisDyskeratosis Congenita E Ectodermal Dysplasia EhlersDanlos Syndrome http://www.genetics.com.au/conditions/main.htm
Portal Toolkit Invalid Site URL syndromes such as Cohen syndrome, Degos disease, and dubowitz syndrome. the second reported case of cataracts in a child with dubowitz syndrome. http://www.co-ophthalmology.com/pt/re/coophth/fulltext.00055735-200212000-00013.
D - E dubowitz syndrome. See also Craniofacial Disorders; Growth Disorders. DubowitzSyndrome 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.
Health Library - List of diseases starting with D Information From Answers.comABCDEFGHIJKLMNOPQRSTU VWXYZD ercole syndrome. Duane anomaly mental retardation;Duane syndrome; DubinJohnson syndrome; dubowitz syndrome http://12.31.13.113/library/healthguide/en-us/illnessconditions/topic.asp?hwid=n
Dubowitzin Oireyhtymä - Kehitysvammahuollon Tietopankki dubowitz syndrome 1, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Groups, An email support group for those interested in dubowitz syndrome http://www.saunalahti.fi/kup/syndroma/dubowitz.htm
Extractions: Kohdunsisäinen kääpiökasvuisuus Dubowitzin oireyhtymä on hyvin harvinainen sairaus, jota luonnehtii kasvun hidastuminen, lyhytkokoisuus ja poikkeavat kasvonpiirteet. Oireet voivat ilmaantua jo sikiövaiheessa tai heti syntymän jälkeen. Noin puolet oireyhtymään sairastuneista on kehitysvammaisia. Wilroy Tipton ja Summitt (1978) totesivat, että henkisen suorituskyvyn madaltuminen oli ollut useimmiten lievää tai rajatilatasoista. Stanley Jablonskin (1999) mukaan oireyhtymän erikoispiirteitä ovat olleet 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 olleet tavanomaisia. Ääni on ollut erikoisen korkea tai käheä. Leuka on ollut usein pienikokoinen ja nielu vajaakehittynyt. Muina oireina on esiintynyt 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 olleet osa taudinkuvaa.
Rarelink.net - Diagnoselisten Dubowitz Syndrome Du er her Hjem Diagnoselisten dubowitz syndrome dubowitz syndrome,dubowitz syndrome, Dubowitz syndrom, dubowitz syndrome. http://www.rarelink.no/diagnosedetail.jsp?diagnoseId=72
Network Of Care Dual Recovery Anonymous Mental Health (General) dubowitz syndrome dubowitz syndrome Information and Parent Support - dubowitz syndrome. Back to Top http://sacramento.networkofcare.org/aging/library/articleList.cfm?type=Support G
Delayed Development Down Syndrome; Drug Addiction; Drug Withdrawal Syndrome; dubowitz syndrome;Duchenne Muscular Dystrophy; DyggveMelchoir-Clausen yndrome http://www.rogerknapp.com/medical/eci.htm
Extractions: Delayed Development Evaluating children for proper development is sometimes difficult since there is such a wide variety in the rate of different children. Check with your doctor or compare your child with others of the same age. If you have concerns then you should call this Early Childhood Intervention (ECI) line and have your child evaluated. It can't hurt. Satisfy yourself that your child is in the normal range. ECI is paid by the government and can give your child therapy if they are behind the normal range of development or have disabilities. They serve up to age three. ECI services for children: ECI services for families: education and counseling.
Genetic Conditions List Drash syndrome Double Y syndrome Duane syndrome dubowitz syndrome. D2 Hydroxyglutaricacidurdia Dysautonomia Dyschondrosteosis. back to top http://www.agsa-geneticsupport.org.au/conditions_list.html
04.26.2004 dubowitz syndrome. dubowitz syndromeSupport groups adress, WWW links dubowitz syndrome Information and Parent Support http://genetics.rusmedserv.com/catalog/syndlist/
Extractions: E-mail: A B C D ... Z A Aase syndrome Aase syndrome - Pediatric Encyclopedia Acanthosis Nigricans Acanthosis Nigricans Maligna-DermIS Online Atlas Acanthosis Nigricans Benigna-DermIS Online Atlas Achondrogenesis Achondroplasia Acrodermatitis Enteropathica Acrodysostosis Acromegaly Acromesomelic Dysplasia Acromicric Dysplasia ADAM COMPLEX
Haematologica - E-cases The dubowitz syndrome a retrospective. J Craniofac Genet Dev Biol Suppl.1985;12836. 18. Dror Y, Freedman MH. Shwachman-Diamond syndrome An inherited http://www.haematologica.it/e-cases/2003_05/ECR14.htm
Extractions: Abstract Seckel syndrome is a rare autosomal recessive disorder with characteristic craniofacial dysmorphism, skeletal defects, mental and prenatal growth retardation. About 50 cases have been reported in the literature. Hematologic abnormalities with associated chromosomal fragility have been noted in about 15% of the reported cases. We report a patient with Seckel syndrome with myelodysplastic features and clonal T-cells in the bone marrow but no evidence of chromosomal fragility. After 5 years of follow-up, this patient remains asymptomatic without any treatment and with stable peripheral blood counts. Introduction Several investigators have reported increased chromosomal fragility (by MMC breakage analysis) in the bone marrow cells of patients with Seckel syndrome and hematologic disorders and have suggested an analogy to the chromosomal fragility syndromes such as Fanconi's anemia. These reports raised the possibility that a mechanism similar to that of FA may be responsible for the pathogenesis of myelodysplasia or acute leukemia in these reported cases of Seckel syndrome .
Smithâs Recognizable Patterns Of Human Malformation, 6th Edition BrachmannDe Lange Syndrome RubinsteinTaybi Syndrome Russell-Silver Syndrome 3-M Syndrome Mulibrey Nanism Syndrome dubowitz syndrome Bloom Syndrome http://www.intl.elsevierhealth.com/catalogue/title.cfm?ISBN=0721606156
Extractions: Home Site map Regional Sites Advanced Product Search ... Smith's Recognizable Patterns of Human Malformation Book information Product description Audience Author information and services Ordering information Bibliographic and ordering information Book related information Submit your book proposal Other books in same subject area About Elsevier Select your view SMITH'S RECOGNIZABLE PATTERNS OF HUMAN MALFORMATION The completely revised and updated New Edition of this definitive text?now in full color! Long known as the source to consult for guidance on diagnosis, prognosis, plan management, and genetic counseling, this easy-to-use reference focuses on the patterns of human defects caused by inborn errors in morphogenesis as opposed to defects caused by mechanical problems. It provides a wealth of information on normal and abnormal morphogenesis * minor anomalies and their relevance * clinical approaches to specific diagnoses * and normal standards of measurement for the entire spectrum of disorders. Each chapter includes a description of the specific abnormality?including occasional associated abnormalities?natural history, etiology, and references. On opposing pages are several descriptive photographs and line drawings of either an individual with the abnormality or specific features of the abnormality.
IBMFS - Other Bone Marrow Failure Syndromes failure is not thought to be a major feature of the disease. These includedisorders such as Seckel syndrome, dubowitz syndrome, and Down syndrome. http://marrowfailure.cancer.gov/OTHER.html
Extractions: Other Bone Marrow Failure Syndromes There are several other inherited bone marrow syndromes which are less common than the ones that are discussed individually on this Website. These diagnoses are usually made by experts in hematology or genetics. Examples include the following disorders: Revesz (abnormal nails, aplastic anemia , and a problem with the retina, or back of the eye), IVIC (named with the initials of the institution which first reported it), WT (after the initials of the first two families reported), radio-ulnar synostosis (the bones of the lower arm are joined together at the elbow), ataxia pancytopenia (unsteady walking and aplastic anemia). There are families with more than one case with bone marrow failure, who do not fit any of the usual categories. Finally, there are other genetic diseases in which bone marrow failure has been reported on rare occasions, but in which bone marrow failure is not thought to be a major feature of the disease. These include disorders such as Seckel syndrome, Dubowitz syndrome, and Down syndrome. Home Cohort Disorders Participate ... Contact Us
