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61. Homepage Of Philip R. Dodge, M.D.
Acute childhood encephalopathies, transient blindness after minimal trauma, cerebral gigantism, unilateral pupillary dilation with seizure, the bobblehead
http://www.neuro.wustl.edu/people/dodge.html
Department of
Neurology Philip R. Dodge, MD Dr. Dodge is Professor Emeritus in the Departments of Pediatrics and Neurology. BIOGRAPHICAL SKETCH Philip R. Dodge, MD came to Washington University School of Medicine/St. Louis Children's Hospital in 1967 from the Massachusetts General Hospital and Harvard Medical School in Boston, Massachusetts to Chair the Edward Mallinckrodt Department of Pediatrics, a position he held until 1986. Dr. Dodge is one of the modern founders of the specialty of Pediatric Neurology in the United States. After receiving his medical degree from the University of Rochester in 1948, he continued his clinical education in internal medicine there and in neurology and neuropathology at the Boston City Hospital and the Massachusetts General Hospital in Boston. Dr. Dodge is a member of the American Neurological Association, American Academy of Neurology, the American Academy of Pediatrics, American Epilepsy Society, Child Neurology Society, International Child Neurology Association, Society for Pediatric Research, American Pediatric Society, serving as officer of or as committee chair for several of these organizations throughout his membership. He received the Hower Award from the Child Neurology Society in 1978 and the Distinguished Service Award from the Washington University Medical Center Alumni Association in 2000. RESEARCH SUMMARY His interest in children let to his focusing upon child neurology. In collaboration with pediatric colleagues he pursued studies of altered osmolatity of body fluids on function of the nervous system, studied the development and persistence of subdural effusions, and initiated his long standing retrospective and prospective investigations of acute bacterial meningitis on the brain. Acute childhood encephalopathies, transient blindness after minimal trauma, cerebral gigantism, unilateral pupillary dilation with seizure, the bobble-head doll syndrome were among the conditions that arrested his attention and early description. Studies of nutrition and the developing brain culminated in publication of a book authored by Drs. Dodge, Prensky, and Feigin.

62. Malattie Rare E Genetiche Lettera "G"
Translate this page syndrometrichorhinophalangeal dysplasia 1•••{190350-275500} * Gigantismo cerebraleSindrome Sotos•Sotos Syndromecerebral gigantism/Sotos syndrome
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G G Sindrome [Sindrome oculogenitolaringea/ OPITZ SINDROME DI G syndrome G syndrome[Opitz-Frias syndrome/autosomal dominant Opitz syndrome (ADOS)/BBB syndrome/BBBG syndrome/BBB G syndrome/BBG syndrome/G BBB syndrome/hypospadias-dysphagia syndrome/hypertelorism-hypospadias syndrome/oculo-genito-laryngeal syndrome/telecanthus-hypospadias syndrome/X-linked Opitz syndrome (XLOS)] Hiperterorim with Esophageal Abnormality and Hipospadia ... GAUCHER MALATTIA DI [Lipoidosi cerebrosidica/Tesaurismosi cerasinica/Cerebrolipoidosi/Reticulosi accumulativa lipoidea da cerebrosidi/Splenomegalia a grandi cellule lipidiche/sfingolipidosi ereditaria/Tesaurismosi cerasinica/Gaucher Schlagenhaufer Malattia di] Gaucher Malattia di Gaucher Disease Gaucher disease Gaucher, maladie de

63. J Med Genet -- KOK Et Al. 36 (4): 346
Since this report, many cases have been described of what is now known as Sotos syndrome or cerebral gigantism. 2 Most cases appear to be sporadic.
http://www.jmedgenet.com/cgi/content/full/36/4/346

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J Med Genet 346-347 ( April )
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Breakpoint mapping by FISH in a Sotos patient with a constitutional translocation t(3;6)
E DITOR Involvement of region 3p21 of chromosome 3 in the development of Sotos syndrome is suggested by two patients who have been described. One is a Sotos syndrome patient carrying an apparently balanced translocation t(3;6)(p21;p21). The other is a non-smoking female with Sotos syndrome who died of small cell lung cancer at 22 years of age. This type of cancer is characterised by a consistent loss of heterozygosity at 3p21.3. We were able to set up an EBV immortalised lymphoblastoid cell line from a blood sample from the patient with the t(3;6) and show by fluorescent in situ

64. Medical Information Site With Residency Directory, Auctions, Lab
Ataxia 83) Cerebellar Dysmetria 84) Cerebelloretinal Angiomatosis, Familial 85) Cerebral Anoxia 86) Cerebral Concussion 87) cerebral gigantism 88) Cerebral
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65. Soto's Syndrome From Linkspider UK Health Directory
and professionals. Soto s Syndrome Also known as cerebral gigantism, an information sheet compiled by NINDS. MCW Healthlink - An
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    Sotos Syndrome Support Association - Online community for education of professionals and families and to exchange ideas, gather research, and help one another cope. Quarterly newsletters, reference library, annual meetings, and conferences are available to members and professionals.

66. Sandy's Story
ISBN 09740657-0-6. cerebral gigantism. Sotos Syndrome. A chapter is included with the latest information on Sotos syndrome, also known as cerebral gigantism.
http://www.awriteshop.com/Sandy'sStory.html
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Available in eBook format only. Press the "Buy Now" button to order and download your personal copy. ISBN 0-9740657-0-6 Cerebral Gigantism Sotos Syndrome Learn how a young mother struggles to get the appropriate medical, educational and social needs for her child in the late 60’s and early 70’s. Discover how she contends with family, friends and strangers for acceptance of her disabled daughter. Find out how Sandy’s untimely death was due to malpractice because she was disabled. Experience how Sandy’s life and death teaches her mother of the need for reform in the medical, educational and social

67. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/C
Cerebral Edema@ (3); cerebral gigantism@ (5); Cerebral Palsy@ (145); Cerebrocostomandibular Syndrome@ (2); Cerebrohepatorenal Syndrome
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68. Dorlands Medical Dictionary
cerebral gigantism, gigantism in the absence of increased levels of growth hormone, attributed to a cerebral defect; infants are large, and accelerated growth
http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

69. Cardiovascular National Target Human Services David Health Observance Sign Sympt
What is Sotos Syndrome? Sotos Syndrome, also known as cerebral gigantism because of the distinctive head shape and size, is a genetic condition causing physical overgrowth during the
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70. Membres De La SENP
Helv Paediatr Acta 1980;35(1) cerebral gigantism (Sotos syndrome) with juvenile macular degeneration. Ferrier PE, de Meuron G, Korol
http://www.senp-neuropediatrie.org/Annuaire_des_membres/Liste_des_Membres_de_la_
PARU Annuaire de la SENP SUISSE DE MEURON Gilles Adresse : Téléphone : Fax : Abstracts : mireilledemeuron@hotmail.com J Pediatr Surg 2001;35(12)
A case of pediatric Henoch-Schönlein purpura and thrombosis of spermatic veins.
Diana A, Gaze H, Laubscher B, De Meuron G, Tschantz P
Hôpital Pourtalès, Neuchâtel, Switzerland.
The authors report a case of thrombosis of the spermatic veins associated with Henoch-Schönlein purpura mimicking an acute scrotum, which responded to a low-molecular-weight heparin treatment.
PMID: 11101753[PM]
Rev Med Suisse Romande 1998;117(10)
[Management of the handicapped child. Summary of a psychosocial workshop]
Gubser-Mercati D, De Meuron G
no abstract available
PMID: 9441356[PM] J Neurol Sci 1986;75(1) Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie Infantile. Echenne B, Arthuis M, Billard C, Campos-Castello J, Castel Y, Dulac O, Fontan D, Gauthier A, Kulakowski S, De Meuron G PMID: 3091775[PM] Helv Paediatr Acta 1980;35(1) Cerebral gigantism (Sotos syndrome) with juvenile macular degeneration.

71. C Conditions And Diseases Health English
Abscess ? Cerebral Edema English Health Conditions and Diseases Neurological Disorders Brain Diseases Cerebral Edema ? cerebral gigantism English Health
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72. Search By Disease
99 Cerebral cholesterinosis. 100 cerebral gigantism. 101 Cerebral hemorrhage, familial. 102 Cerebral hemorrhage, hereditary, with amyloidosis.
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75. GASNet Anesthesiology: Contents A - C
Central Core. Central Core Disease. cerebral gigantism. Sotos s Syndrome (cerebral gigantism). Cerebrohepatorenal. Bowen Syndrome (Cerebrohepatorenal Syndrome).
http://www.gasnet.org/pediatric-syndromes/a2c_br.php
Contents A - C - pediatric syndromes - Acidosis Fanconi's Syndrome (Renal Tubular Acidosis) Albers Albers - Schönberg Disease (Osteopetrosis, Marble Bone Disease) Albright Albright - Butler Syndrome (Primary Distal Renal Tubular Acidosis) Albright McCune - Albright Syndrome Aldrich Wiskott - Aldrich Alström Alström Syndrome Analbumenia Analbumenia Analphalipoproteinemia Tangier Disease (Analphalipoproteinemia) Andersen Andersen Disease (Glycogen Storage Disease Type IV) Anderson Anderson Syndrome Angelman Angelman's Syndrome Angioneurotic Hereditary Angioneurotic Edema Angioosteohypertrophy Klippel - Trenaunay Syndrome (Angioosteohypertrophy) Anhydrotic Christ - Siemens - Touraine Syndrome (Anhydrotic Ectodermal Dysplasia) Apert Apert Syndrome Arnold Arnold - Chiari Malformation Arthogryposis Arthogryposis Multiplex Congenita Asphyxiating Jeune's Syndrome (Asphyxiating Thoracic Dystrophy) Ataxia Ataxia - Telangiectasia Ataxia Friedreich's Ataxia Auricular Goldenhar Syndrome (Auriculo Vertebral Syndrome) Bardet Bardet - Biedl Syndrome Barré Guillain - Barré Syndrome Bartter Bartter Syndrome Bassen Bassen - Kornzweig Syndrome Beckwith Beckwith - Wiedemann Syndrome Behçet Behçet Syndrome Blackfan Blackfan - Diamond Syndrome Biedl Bardet - Biedl Syndrome Biedl Lawrence - Moon - Biedl Syndrome Bloch Bloch - Sulzberger Syndrome Bowen Bowen Syndrome (Cerebrohepatorenal Syndrome) Bullae Cockayne - Touraine Syndrome (Dystrophic Epidermolysis Bullae) Butler Albright - Butler Syndrome (Primary Distal Renal Tubular Acidosis) Carpenter Carpenter Syndrome Central Core

76. Arch Pediatr Adolesc Med -- Abstracts: Maldonado Et Al. 138 (5): 486
cerebral gigantism associated with Wilms tumor. V Two children had cerebral gigantism in unique association with Wilms tumor. An
http://archpedi.ama-assn.org/cgi/content/abstract/138/5/486
Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA For The Media Classified Ads Meetings Peer Review Congress
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Cerebral gigantism associated with Wilms' tumor
V. Maldonado, P. S. Gaynon and A. K. Poznanski
Two children had cerebral gigantism in unique association with Wilms' tumor. An increased incidence of neoplasms has been reported in cerebral gigantism, as well as in Beckwith-Wiedemann syndrome. We report similarities and differences between these disorders.
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77. Arch Pediatr Adolesc Med -- Table Of Contents (Vol. 131 No. 6, June 1977)
ARTICLES. cerebral gigantism JF Sotos; EA Cutler; P. Dodre Am J Dis Child. 1977;131625627. The child health associate ML Peterson Am J Dis Child.
http://archpedi.ama-assn.org/content/vol131/issue6/index.dtl
Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA For The Media Classified Ads Meetings Peer Review Congress
Vol. 131 No. 6, pp. 625-930, June 1977 Content Access Sign in/out Activate online subscription One-time access Individual subscriptions ... Register for E-mail Alerts Table of Contents Jump to Section ARTICLES
ARTICLES Cerebral gigantism
J. F. Sotos; E. A. Cutler; P. Dodre
Am J Dis Child.
The child health associate
M. L. Peterson
Am J Dis Child.
A case of cerebral gigantism and hepatocarcinoma
G. I. Sugarman; E. T. Heuser; W. B. Reed
Am J Dis Child. ABSTRACT The pediatric practice of the child health associate L. L. Fine Am J Dis Child. ABSTRACT Preventive medicineprofessed much, practiced little A. B. Bergman Am J Dis Child. Hepatitis B surface antigen and chronic hepatitis in infants born to asymptomatic carrier mothers K. Shiraki; N. Yoshihara; T. Kawana; H. Yasui; M. Sakurai Am J Dis Child.

78. YOUNG ONSET NEUROLOGICAL DISEASE ASSOCIATION Br YONDA For Short
Central Pain Syndrome, Cephalic Disorders , Cerebral Aneurysm, Cerebral Arteriosclerosis, Cerebral Atrophy, cerebral gigantism, Cerebral Palsy , CharcotMarie
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79. C Index
CEREBELLOOCULOCUTANEOUS TELANGIECTASIA. CEREBELLORETINAL HEMANGIOBLASTOMATOSIS. cerebral gigantism. Please click on the box below to view the following topics.
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80. FAIVRE L
GOSSET P., ROMANA S., MUNNICH A., VEKEMANS M., CORMIER DAIRE V. Apparent sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2p12.1 mosaicism.
http://www.necker.fr/irnem/Unites 2000/histo.htm
FAIVRE L., PRIEUR A.M., LE MERRER M., HAYEM F., PENET C., WOO P., HOFER M., DAGONEAU N., SERMET I., MUNNICH A., CORMIER-DAIRE V.
Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Amer. J. Med. Genet.,
(Services cités :
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is an autosomal recessive condition characterized by the association of congenital or early onset camptodactyly and noninflammatory arthropathy with synovial hyperplasia, Progressive coxa vara deformity and/or noninflammatory pericardial or pleural effusions have been observed in some patients, Recently, the disease gene has been assigned to human chromosome region 1q25-q31, and truncating mutations have been identified in the megakaryocyte stimulating factor gene, Studying 12 patients from 8 unrelated families, we emphasized hip and spine involvement, particularly in the course of the disease as shown in a 58-year-old patient. Despite clinical variability, linkage studies support genetic homogeneity of the disease. [References: 25] FAIVRE L., VIOT G., PRIEUR M., TURLEAU C., GOSSET P., ROMANA S., MUNNICH A., VEKEMANS M., CORMIER DAIRE V.

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