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Craniofrontonasal Dysplasia:     more detail

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61. Conditions And Diseases: Genetic Disorders: Craniofrontonasal Dysplasia
    Health and Home. craniofrontonasal dysplasia. htbinpost/Omim/dispmim?304110.craniofrontonasal dysplasia. Last Update Mon May 10 2004.  
    http://www.health-home.net/Conditions_and_Diseases/Genetic_Disorders/Craniofront

62. Healthwise
    Topic craniofrontonasal dysplasia, Back to previous page. SynonymsDisorder Subdivisions General Discussion Resources National  
    http://www.stlukes-sf.org/health/healthinfo/index.cfm?section=healthinfo&page=ar

63. Frontonasal Dysplasia
    A. Oculoauricular-vertebral spectrum. B. Frontofacionasal dysostosis – autosomalrecessive inheritance. C. craniofrontonasal dysplasia. VII. Resources.  
    http://www.genesoc.com/counseling/Outlines/frontonasaldysplasia.htm
    
    Extractions: Resources for Genetic Counselors site updated May 10, 2004 outlines links search Frontonasal Dysplasia (Median Cleft Face Syndrome) I. Contracting A. How have things been going since your last visit? B. What questions or concerns would you like to address today? II. Interim History A. Which physicians are you seeing? When are your follow-up appointments scheduled? B. Recent tests: video swallowing study, audiologic evaluation, O saturation studies? C. How have things been going since the cleft palate repair? Any complications? Current feeding issues? D. Developmental assessment questions Rolling over? Sitting when supported? Pincher grasp? Reaching for objects? Babbling? Any consonant sounds? Words? E. Are you satisfied with OT/PT services? Have you noticed improvements? III. Psychosocial Assessment A. Who lives in the home with you? B. Are you working outside the home? Who cares for him when you are at work? C. Do you have any help with his care? Do you feel like you need help? D.

64. Free Genealogy Search :: Health : Conditions_and_Diseases : Genetic_Disorders :
    NORD craniofrontonasal dysplasia Offers a general discussion andresources. » OMIM National Center for Biotechnology Information  
    http://www.lineages.co.uk/dwodp/index.php/Health/Conditions_and_Diseases/Genetic
    
    Extractions: @import url( http://www.lineages.co.uk/wp-layout.css ); Search: search the entire directory search this category only Top Health See also: Health: Conditions and Diseases: Rare Disorders National Library of Medicine: CNFS - Offers synonyms of craniofrontonasal syndrome, a summary and a list of features.

65. Orthopaedic Syndromes First Page
    deafnesshand syndrome; craniofrontonasal dysplasia; Craniometaphysealdysplasia; Craniosynostosis, Adelaide type; Craniosynostosis, type  
    http://freeortho.com/syndromes.html
    
    Extractions: Click on the syndromes for further details: A B C D ... H I J K L M ... P Q R S T U V W X Y Z OMIM Database ALL Syndromes - Clinical Features University of Western Ontario - Paediatric Database Gene maping and Other details: Achondrogenesis Ib Achondrogenesis-hypochondrogenesis, type II Achondroplasia Acrocallosal syndrome ... XLA and isolated growth hormone deficiency

66. Diseases
    Coffin Lowry Syndrome. Costello Syndrome. Cowden Syndrome. craniofrontonasal dysplasia.CriglerNajjar Syndrome. Cystic Fibrosis. Camps. CFTR and Genetic Mutations.  
    http://diseases.health.designerz.com/diseases-directory.php

67. Startplane /Health/Conditions_and_Diseases/Genetic_Disorders/Craniofrontonasal_D
    craniofrontonasal dysplasia. See also Top/Health/Conditions and Diseases/C. Links.NORD craniofrontonasal dysplasia Offers a general discussion and resources.  
    http://www.startplane.com/Health/Conditions_and_Diseases/Genetic_Disorders/Crani

68. Lukol Directory - Health Conditions And Diseases Genetic Disorders
    Costello Syndrome (2). Cowden Syndrome (3). craniofrontonasal dysplasia (3).Cri du Chat Syndrome (5). CriglerNajjar Syndrome (5). Cystic Fibrosis (185).  
    http://www.lukol.com/Top/Health/Conditions_and_Diseases/Genetic_Disorders/

69. Karger Publishers
    Copyright © 2002 S. Karger AG, Basel. goto top of outline Introduction. Craniofrontonasalsyndrome (CFNS) is a subgroup of craniofrontonasal dysplasia (CFND).  
    http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=

70. AOJ 52:58 "Ocular Aspects Of Craniofacial Disorders"
    syndromic synostoses but the most common craniosynostoses include Pfeiffer, Crouzon,Apert, SaethreChotzen, Jackson-Weiss and craniofrontonasal dysplasia.  
    http://www.aoj.org/abstracts/52/52_58.html
    
    Extractions: Am Orthopt J 52:58 (2002). John Pratt-Johnson Lecture Ocular Aspects of Craniofacial Disorders Ken K. Nischal, F.R.C., Ophth. Craniofacial disorders may comprise various entities such as clefting anomalies, tumors, e.g., fibrous dysplasia, orbito-facio-cranial trauma, and the craniosynostoses. Each may have significant ocular involvement but the focus of my discussion is the craniosynostoses. Craniosynostosis is the premature closure of one or more cranial sutures and this may be associated with systemic features or an isolated finding. When a suture closes prematurely growth of the skull continues parallel to the suture but is arrested or retarded perpendicular to it. This results in an irregular shape of the skull. Previously patients with suture synostosis were described as having a particular shaped head such as plagiocephaly, brachycephaly, or scaphocephaly to name a few. These are now better described in terms of the sutures involved, e.g., plagiocephaly is better described as unicoronal synostosis, brachycephaly as bicoronal synostosis, and scaphocephaly as sagittal synostosis. © 2002 The Board of Regents of the University of Wisconsin System

71. A Listing Of Disorders
    Corticobasal Degeneration. Costello Syndrome. craniofrontonasal dysplasia.Craniometaphyseal Dysplasia. Craniosynostosis, Primary. Cri du Chat Syndrome.  
    http://medschool.umaryland.edu/BTBank/Family/Disorders_C.htm
    
    Extractions: University of Maryland, Baltimore C C Syndrome Camptomelic Syndrome Carbamyl Phosphate Synthetase Deficiency Carbohydrate deficient Glycoprotein Syndrome Type Ia Carboxylase Deficiency, Multiple Carcinoid Syndrome Cardio Auditory Syndrome Cardiofaciocutaneous Syndrome Carnitine Deficiency Syndromes Carnitine Palmitoyltransferase Deficiency Carnosinemia Caroli Disease Carpenter Syndrome Castleman's Disease Cat Eye Syndrome Cataract Dental Syndrome Cataracts Catel Manzke Syndrome Caudal Regression Syndrome Cavernous Hemangioma Cayler Syndrome Central Core Disease Central Hypoventilation Syndrome, Congenital Cerebellar Agenesis Cerebellar Degeneration, Subacute Cerebral Palsy Cerebro Oculo Facio Skeletal Syndrome Cerebrocostomandibular Syndrome Chandler's Syndrome Charcot Marie Tooth Disease CHARGE Association Chediak Higashi Syndrome Chiari Frommel Syndrome Chikungunya Cholangitis, Primary Sclerosing Cholecystitis Chondrocalcinosis, Familial Articular Choroideremia Choroiditis, Serpiginous Chromosome 1, Trisomy Chromosome 3, Monosomy 3p2

72. SearchBug Directory: Health: Conditions_and_Diseases: Genetic_Disorders
    2) Congenital Urological Disorders (29) Cornelia De Lange Syndrome (4) CostelloSyndrome (2) Cowden Syndrome (3) craniofrontonasal dysplasia (3) Cri du Chat  
    http://www.searchbug.com/directory.aspx/Health/Conditions_and_Diseases/Genetic_D

73. Hum. Mol. Genet. -- Feldman Et Al. 6 (11): 1937
    4 Cohen , MM , Jr ( 1979 ) craniofrontonasal dysplasia. 10 Kapusta , L. , Brunner,HG and Hamel, BCJ ( 1992 ) craniofrontonasal dysplasia. Eur. J. Pediatr..  
    http://hmg.oupjournals.org/cgi/content/full/6/11/1937
    
    Extractions: References George J. Feldman Deeann E. Ward Elisabeth Lajeunie-Renier Dolores Saavedra Nathaniel H. Robin Virginia Proud Laura J. Robb Vazken Der Kaloustian John C. Carey M. Michael Cohen, Jr Valerie Cormier Arnold Munnich Elaine H. Zackai Andrew O. M. Wilkie R. Arlen Price and Maximilian Muenke The Children's Hospital of Philadelphia, Division of Human Genetics and Molecular Biology, and Departments of Pediatrics, Genetics and Psychiatry, University of Pennsylvania School of Medicine

74. NORD Rare Disease - Medical Transcription At Medword
    Corneal Dystrophy Cornelia de Lange Syndrome Corticobasal Degeneration CostelloSyndrome Cowpox craniofrontonasal dysplasia Craniometaphyseal Dysplasia  
    http://www.medword.com/rardisC.html
    
    Extractions: This listing of rare diseases is provided for spelling reference. Clicking on the link will generate a new window and take you to NORD's home page, where you may search for an abstract of the disease or order a full text report of the disease. Please read the notice at the bottom of this page before using this list. Please use the above list at your own risk. While we make every effort to ensure accuracy, we cannot be held responsible for errors in spelling or capitalization, or any circumstance that may result because of said error. In using the above list you also agree to never hold ANSO Consulting Inc. or Medword Medical Transcription responsible for any errors should they exist. Please Note:

75. ORPHANET - Rare Diseases - Orphan Drugs
    Printing version, DISEASE craniofrontonasal syndrome teebi type, Synonym(s)Brachycephalofrontonasal dysplasia Teebi syndrome, No description is available,  
    http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1519

76. Mioti: Diseases + Conditions
    Information from the National Organization for Rare Disorders. NORD CraniofrontonasalDysplasia. Information from the National Organization for Rare Disorders.  
    http://www.mioti.com/cat/condition/condition.asp?Cat=Dysplasia

77. PHP-Nuke Canada Site - Links
    http//www.fibrosingmediastinitis.com Fibrous dysplasia Support Online For thoseseeking support and information concerning the rare bone diseases fibrous  
    http://www.phpnuke-ca.com/Links-Health__Conditions_and_Diseases__Rare_Disorders_
    
    Extractions: Albanian Arabic Brazilian Catala Chinese Czech Danish Dutch English Euskara Finnish French Galego German Greek Hungarian Icelandic Indonesian Italian Macedonian Norwegian Polish Portuguese Romanian Russian Slovak Slovenian Spanish Swedish Thai Turkish Ukrainian Vietnamese Add your link You are her : /Health/Conditions_and_Diseases/Rare_Disorders/

78. Redirect
    http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?304110

79. Healthcyclopedia Index - C
    Cor Pulmonale, Costello Syndrome. Costochondritis, Cowden Syndrome. CraniofrontonasalDysplasia, Craniosynostosis. Creutzfeldt Jakob Disease, CriglerNajjar Syndrome.  
    http://www.healthcyclopedia.com/c.html

80. ORPHANET - Rare Diseases - Orphan Drugs
    Contact, Order the Orphanet book, Printing version, DISEASE Craniofrontonasaldysplasia, ICD Q75.8, No description is available, MIM 304110, Clinical signs(32),  
    http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1520

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