81. Medical Experts - Cornelia De Lange Syndrome ASSOCIATIONS. Bar Associations Legal Associations Law Firms Attorneys. MedicalExperts cornelia de lange syndrome. AMFS, Inc. (American Medical Forensics). http://www.hg.org/experts/Medical-Experts-Cornelia-de-Lange-Syndrome.html

#1 Legal Research Center Home Law Firms Experts/Consultants Law Practice ... Contact Us LEGAL DIRECTORIES Law Firms Experts/Consultants Investigators Process Servers ... Legal Services LAW PRACTICE 70 Areas of Practice Practice of Law Law Events Calendar Add your Event EMPLOYMENT CENTER Recruiters HG Classified Other Resources STUDENTS CENTER Pre-Law Law Schools Graduate Schools Law Bar ... Other Resources BUSINESS CENTER Starting a Business Ecommerce Legal Structures Financing ... Employment CONSUMERS CENTER Consumer Resources National Regimes Publications Associations UNITED STATES LAW Federal Government States Law INTERNATIONAL LAW 230 Countries United Nations European Union Other Organizations ASSOCIATIONS Bar Associations Legal Associations Law Firms Attorneys Medical Experts: Cornelia de Lange Syndrome AMFS, Inc. (American Medical Forensics) Berkeley, California Contact: Dr. Barry Gustin Tel: 800-275-8903, Fax: 510-486-1255 AMFS is recognized as a leader in the field of medical-legal case review and expert witness testimony. Since 1990 in more than 35,000 medical-legal cases for plaintiff and defendant, AMFS experts have consistently delivered. AMFS is the only medical forensic consulting group staffed exclusively by board-certified in-house physicians. Extended Information Mailing Lists Add your Firm Contact Us H ieros G

82. Children's Charities Of America cornelia de lange syndrome Foundation. 302 When we were first told thatour baby had cornelia de lange syndrome, we were crushed. My http://www.childrenscharities.org/ccamemdetail.asp?ORGID=541

83. CdLSWORLD CdLSWORLD. Home. What is cornelia de lange syndrome? A Syndrome is a medical term for a condition in which there is a collection http://www.cdlsworld.org/about_cdls.html

Home What is Cornelia de Lange Syndrome? A "Syndrome" is a medical term for a condition in which there is a collection of signs (observable body changes) and symptoms (problems related by the patient) recognizable by a doctor's exam. Individuals with a syndrome may not have all of its associated signs and symptoms, but they must have enough to be considered "diagnostic." Conversely, because someone may display some of the signs and symptoms of a syndrome, does not necessarily mean they have it. In 1933, Dr. Cornelia de Lange, a Dutch pediatrician, described two children with similar features, one 17 months and the other 6 months, who were admitted within weeks of each other to Emma Children's Hospital. The first child had pneumonia. Her first year of life had been characterized by a lot of feeding difficulties and she was very small for her age, with a proportionately smaller head circumference. Other unusual facial characteristics were noted by Dr. de Lange. Soon after this child was discharged, a second little girl was admitted. Not only did they have common medical problems, but their resemblance to each other was remarkable. In each case the doctor described what she observed with great care and detail. Professor de Lange followed her own advice: "Observe closely first." Nowhere was the puzzled physician able to find a similar patient described in medical literature. Cornelia de Lange is now generally credited with describing the collection of symptoms comprising the syndrome that bears her name.

84. QU'EST-CE QUE LE SYNDROME DE CORNELIA DE LANGE ? Translate this page QU'EST-CE QUE LE syndrome de cornelia de lange ? http://orphanet.infobiogen.fr/associations/AFSCDL/AFSCDL.html

QU'EST-CE QUE LE SYNDROME DE CORNELIA DE LANGE ? QU'EST-CE QUE LE SYNDROME DE CORNELIA DE LANGE ? QUELS EN SONT LES SYMPTOMES ET LES MANIFESTATIONS ? EVOLUTION QUE PEUT-ON FAIRE ? ... Nous contacter Le mot syndrome est le terme médical pour désigner un ensemble de signes ou de symptômes reliés, à une cause commune. Le syndrome de Cornelia de Lange (SCDL) vient du nom du Professeur Cornelia de Lange, pédiatre hollandaise, qui a écrit en 1933, un article décrivant deux enfants. Il est parfois appelé le syndrome Brachmann - De Lange, car le Docteur Brachmann décrivit un patient similaire en 1916. C'est un syndrome rare, sa fréquence est de l'ordre de 1 pour 20 000 naissances. Il n'existe pas de critère unique pour établir un diagnostic définitif. La variabilité en est telle que seul un généticien expérimenté ou un médecin familiarisé avec le syndrome peuvent l'évoquer. Y-a-t'il différentes formes d'atteintes ? Oui . De nombreux médecins appellent syndrome Cornelia de Lange "classique" la forme sévère, et "modérée" la forme qui touche les enfants moins sévèrement atteints. Qu'elle est la cause ?

85. Brachmann-de Lange Syndrome (www.whonamedit.com) Amstelodamensis. Also known as cornelia de lange's syndrome,Brachmanncorneliade lange syndrome,de lange’s syndrome. Who named it? http://www.whonamedit.com/synd.cfm/1080.html

Home List categories Eponyms A-Z Biographies by country ... Contact Brachmann-de Lange syndrome Also known as: Cornelia de Lange's syndrome Brachmann-Cornelia de Lange syndrome de Lange’s syndrome Associated persons: Winfried Robert Clemens Brachmann Cornelia Catharina de Lange Description: This condition is described sometimes as one syndrome, sometimes as two. It is here entered as one entity. A rare form of oligophrenia comprising microcephaly with severe mental retardation, short stature, and characteristic facies. Craniofacial features consist of a clown-like appearance with large, low and curly eyelashes, micrognathia, thin lips and downturned upper lip (carp mouth), cleft lip and palate, optic atrophy, an upturned nose, and hirsutism. The most striking feature of the syndrome is that all the children look alike, like brothers and sisters. Often severe dysplasia of extremities. There is a lobster-claw deformity of the hand, small hands and feet with small and tapered digits, syndactyly between the second and third toes, proximal insertion of the thumb, short and curved fifth finger, phocomelia, and oligodactyly. various other malformations. Cutis marmorata, circumoral cyanosis, generalized hypertrichosis, hypoplastic nipples and umbilicus, and simian creases are the principal dermatological features. Low birth weight after full-term pregnancy and a low-pitched growling cry are the early symptoms. The majority of those affected have diminished sucking and swallowing capacity, failure to thrive, predisposition to respiratory tract infections, and frequent vomiting with aspiration pneumonia. Mental retardation is usually severe. Most patients die before the age of 6 years. The aetiology is unknown.

86. Cornelia Catharina De Lange (www.whonamedit.com) cornelia Catharina de lange Dutch paediatrician, born June 24, 1871, Alkmaar;died January 28, 1950. Associated with Brachmannde lange syndrome,Bruck-de http://www.whonamedit.com/doctor.cfm/1059.html

Home List categories Eponyms A-Z Biographies by country ... Contact Cornelia Catharina de Lange Dutch paediatrician, born June 24, 1871, Alkmaar; died January 28, 1950. Associated eponyms: Brachmann-de Lange syndrome Amstelodamensis typus degenerativus, Amsterdam degeneration type Lange, Amsterdam dwarf, congenital (embryological) malformation syndrome, typus degenerativus Amstelodamensis. Bruck-de Lange disease A congenital syndrome of muscular hypertrophy, extrapyramidal disorders, and mental deficiency. Biography: Cornelia Catharina de Lange crossed the prejudices of her time, studying to become a physician. She worked for half a century to improve the healthcare of children. Cornelia Catharina de Lange was born in Alkmaar and received her education in that town, attending the hogere burgerschool - the Citizen's high school. She then wanted to study medicine, but in accordance with the views of the time her father considered the medical profession inappropriate for a woman, and wanted his daughter to study chemistry. She commenced her chemical studies at the University of Amsterdam in 1891, but subsequently changed courses as her father had changed his opinion, and graduated in medicine in 1897. She was conferred doctor of medicine the same year. Cornelia de Lange settled as a general practitioner in Amsterdam, with a special interest in paediatrics. After a four month visit to the Kinderspital in Zurich, she established her own paediatric reception, soon busy and highly appreciated by Dutch mothers. In 1907 she was appointed physician to the Emma Kinderziekenhuis, where a new infants ward was established on her initiative.

87. HONselect - De Lange Syndrome Translate this page English de lange syndrome, - Brachmann-de lange syndrome - cornelia de langesyndrome - de lange's syndrome - Typus degenerativus Amstelodamensis http://www.hon.ch/HONselect/RareDiseases/C10.271.300.html

List of rare diseases: English Deutsch Language: MeSH term: Accepted terms: English: De Lange Syndrome - Brachmann-De Lange Syndrome - Cornelia De Lange Syndrome - De Lange's Syndrome - Typus Degenerativus Amstelodamensis - Amstelodamensis, Typus Degenerativus - Brachmann De Lange Syndrome Français: DE LANGE, SYNDROME - CORNELIA DE LANGE, SYNDROME - SYNDROME DE LANGE Deutsch: De-Lange-Syndrom - Geistige Behinderung - Brachmann-De-Lange Syndrom - Cornelia-De-Lange-Syndrom Español: SINDROME DE DE LANGE - SINDROME DE BRACHMANN-DE LANGE - SINDROME DE CORNELIA DE LANGE Português: SINDROME DE DE LANGE - SINDROME DE BRACKMANN-DE LANGE - SINDROME DE CORNELIA DE LANGE HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: No Web sites: English Yes Français No Deutsch No Español Yes Português No Home About us Site map Feedback ... HONewsletter http://www.hon.ch/HONselect/RareDiseases/C10.271.300.html Last modified: Thu Jul 25 2002

88. Cornélia De Lange (syndrome De) Translate this page réalisée par Jackson et coll. en 1993, en association avec la Corneliade lange syndrome Foundation. Causes Elles ne sont pas http://www.vulgaris-medical.com/textc/cornelia.html

Cornélia de Lange (syndrome de) Synonymes : SCDL, syndrome Brachmann, typus amstelodamensis. Syndrome rare (fréquence de l'ordre de 1 pour 20 000 naissances) décrit par un professeur de pédiatrie : Cornelia de Lange, pédiatre hollandaise. Ce syndrome est un ensemble d'anomalies qui se caractérisent par des malformations du visage associées à un retard de croissance avant et après la naissance. D'autre part, les enfants atteints du syndrome de Cornelia de Lange présentent un retard intellectuel plus ou moins marqué et quelquefois des anomalies des membres supérieurs. Le docteur Cornelia de Lange était professeur à Amsterdam où elle décrit pour la première fois en 1933 les signes cliniques de deux jeunes filles présentant les anomalies du syndrome connu aujourd'hui sous le nom de syndrome de Cornelia de Lange ou syndrome de Brachmann-de Lange (SBdL) en mémoire au Dr Brachmann, un Allemand qui en 1916 a décrit les résultats d'une autopsie faite sur un enfant qui présentait des défauts sévères touchant le cubitus et les mains (qui n'avaient qu'un seul doigt) associés au syndrome (ensemble de signes) décrits ci-après. On distingue habituellement la forme classique (forme sévère) et la forme modérée. Les signes décrits ci-après tiennent compte de l'étude clinique sur 310 individus qui ait été réalisée par Jackson et coll. en 1993, en association avec la Cornelia de Lange Syndrome Foundation.

89. De Lange, Syndrome : Sites Et Documents Francophones syndrome de lange . Voir aussi retardmental . texte syndrome de cornelia de lange Par M. Roger D, M. Dufort JY. http://www.chu-rouen.fr/ssf/pathol/delangesyndrome.html

De Lange, Syndrome Menu général CISMeF Synonyme(s) cornelia de lange, syndrome ; syndrome de lange Voir aussi retard mental Arborescence(s) De Lange, syndrome De Lange syndrome maladies et malformations congénitales, héréditaires et néonatales système nerveux, maladies Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter toutes les ressources ou seulement les principales ou utiliser l' outil de recherche les recommandations les documents concernant l' enseignement les documents destinés aux patients Ou consulter ci-dessous une sélection des principales ressources : patient AFSCDL - Association Française du Syndrome de Cornelia de Lange [Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. Direction Générale de la Santé / INSERM ; ; langue : français ; format : html ; accès : gratuit ; non parrainé ; visité le : 13/12/2000]. mots clés : * De Lange, syndrome type(s) : association patients texte Syndrome de Cornelia de Lange [Par M. Roger D, M. Dufort JY. Site éditeur Centres Butters-Savoye et Horizon ; langue : français ; format : html ; accès : gratuit ; non parrainé ; visité le : 13/12/2000].

90. Cornelia De Lange's Syndrome cornelia de lange's syndrome. BASICS deSCRIPTION respiratory failure. ICD9-CM759.8 cornelia de lange's syndrome Date last updated 9/11/01 http://www.5mcc.com/Assets/SUMMARY/0232.html

91. Le Syndrome De Cornelia De Lange syndrome de cornelia de lange. Maladiesrares. Le syndrome de cornelia de lange. Du nom d'une pédiatre http://www.essentielsante.net/Html/MaladiesRares/cadre/120058200.htm

Accueil Maladies rares Le syndrome de Cornelia de Lange Maladies rares Le syndrome de Cornelia de Lange Du nom d'une pédiatre hollandaise qui en fit la description il y a 60 ans, le syndrome de Cornelia de Lange, ou SCDL, associe entre autres des malformations faciales, rénales, cardiaques et un retard de croissance. Ce syndrome est très varié d'un enfant à l'autre, d'où la difficulté du diagnostic. Le diagnostic de SCDL repose sur la constatation d’une cinquantaine de signes, la plupart très discrets. Malheureusement, cette maladie génétique orpheline, qui touche une naissance sur 20 000 environ, est très polymorphe, c'est-à-dire que les signes n'ont pas la même intensité chez tous les sujets atteints, voire manquent parfois. Le SCDL peut être typique ou frustre, selon les cas. Certains SCDL ont un faciès proche de la normale ! Le diagnostic reste donc difficile, surtout dans les premiers mois et années de la vie. En général, les enfants touchés ont un retard de croissance staturo-pondéral, un petit poids à la naissance et ont du mal à téter. Typiquement, mais c'est rarement le cas, le SCDL comporte des traits particuliers du visage, comme des sourcils fournis et épais se rejoignant à la racine du nez, des cils épais et recourbés, un nez court et petit à racine large, des lèvres minces et parfois des oreilles implantées un peu bas. Il existe parfois un hirsutisme. Le périmètre cérébral est diminué. Des malformations cardiaques et rénales sont parfois observées. La petite taille est habituelle. Une incurvation de l'auriculaire et des anomalies des orteils, peuvent mettre la puce à l'oreille. Un reflux gastro-œsophagien est fréquent.

92. Cornelia De Lange's Syndrome cornelia de lange's syndrome,, Print this article, (cornelia de lange, 1871–1950,Dutch paediatrician), (also known as Brachman de lange syndrome). http://www.amershamhealth.com/medcyclopaedia/Volume VII/Cornelia de Langes syndr

Medcyclopaedia About Medcyclopaedia Amersham Health Search for: Type a word or a phrase. All forms of the word are searchable. Advanced search Browse entry words starting with: A B C D ... Other characters Try our Medcyclopaedia Premium Edition with added tools and functionality tailored to make your working day easier. The following tools are presently available: Expanded search *For Medical Professionals only, registration required Cornelia de lange's syndrome, (Cornelia de Lange, 1871–1950, Dutch paediatrician), (also known as Brachman de Lange syndrome). The clinical features include low birth weight, facial features which include heavy eyebrows, curly eyelashes, an upturned nose and low hairline, and mental and motor retardation. Radiologically there is microcephaly and limb anomalies, including phocomelia, hemimelia and both oligo- and syndactyly, dislocation of the radial head and retarded bone age. Congenital heart disease is a relatively common feature. The diagnosis of an abnormal fetus is often made prenatally. HC The Encyclopaedia of Medical Imaging Volume VII Welcome to Medcyclopaedia.

93. Kindheit Und Entwicklung, 1998 / 2 Translate this page cornelia-de-lange syndrome with severe mental retardation Behavioral and developmentalprofile. Klaus Sarimski. Kinderzentrum München Zusammenfassung http://www.hogrefe.de/ke/ke9802.html

Kindheit und Entwicklung, 1998 / 2 Does a behavioral phenotype exist in nocturnal enuresis? Alexander von Gontard Abstract: Nocturnal enuresis is a phenotypically and clinically heterogeneous disorder with positive linkage to markers on chromosomes No. 8, 12 and 13, leading to the trait of a maturational dysfunction of the CNS. Signs include deep sleep and lack of arousal, neurological, neurophysiological and endocrinological changes and a disposition towards wetting when exposed to stressors. In contrast, there is no peripheral bladder dysfunction. A behavioral phenotype can be identified for subgroups of enuresis. There is a low psychiatric comorbidity in primary, and a high rate of behavioral disorders and stressful life events in secondary nocturnal enuresis. Due to clinical and genetic heterogeneity, a clear association between phenotype and genotype does not exist. Key words: nocturnal enuresis, primary nocturnal enuresis, secondary nocturnal enuresis, monosymptomatic nocturnal enuresis, genotype, phenotype, psychiatric comorbidity, linkage studies Das fragile X-Syndrom The fragile X-syndrome Jochen Schreck, Margitta Backes, Alexander von Gontard und Gerd Lehmkuhl

94. AD HOC BIBLIO - INDEX SUJETS LETTRE C Compilé Le 14/01/03 Galactosaemia .m; Classical Phenylketonuria .m; Corneliade lange syndrome .m; Cri du chat syndrome .m; Down syndrome http://www.cidg.com/~marienf/k/i/mid3c.htm

C Achieving independence by a high level quadriplegic through motivation and techn... [m] Assessment for therapeutic positioning in seating in the C.P. population.... [m] Bead seat re-visited.... [m] Clinical performance of scooters and power based wheelchairs users using a power... [m] How to evaluate a pressure relief cushion: A literature review.... [m] Innovations in therapeutic positioning. The use of "Adaptfoam" for quick customi... [m] Issues in developing custom car seats for young children with physical disabilit... [m] Seating and mobility considerations for children with Duchenne Muscular dystroph... [m] The effects of saddle seating on trunk posture, postural sway, and upper-extremi... [m] Abstracts of the 21st Annual Carrell-Krusen Symposium, Dallas, TX, february 24-... [a] [m] [m] [m] [m] Le cerveau des enfants atteints d'autisme : nouvelles explorations.... [m] [m] [m] Congres : Eigth Annual Conference on Gait Analysis, St. Paul, MI, March 1998... Summary of pathologic gait.... [m] Congres : Eigth Annual Conference on Gait Analysis, St. Paul, MI, March 1998... Assessing functional outcomes....

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

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 ... Neurological Disorders > Chromosomal 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

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