21. Cerebrocostomandibular Syndrome Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/CEREBROCOSTOMAND

financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Cerebrocostomandibular syndrome, rare syndrome in which the dominant radiological abnormality is gaps in the posterior rib shafts due to replacement of normal rib by cartilaginous or fibrous tissue ( Fig.1 ). This can lead to a flail chest and respiratory difficulty. Other features of the syndrome are micrognathia, which is always present, and variable reports of mental retardation and congenital brain anomalies. Most cases are sporadic but autosomal dominant inheritance is known. HC The Encyclopaedia of Medical Imaging Volume VII Cerebrocostomandibular syndrome, Fig. 1 Newborn infant. Note the rib gaps, typical of this syndrome. The child also had heart disease. (Courtesy of Dr. Palaniappan) Corporate Products Financial Services Our Commitment ... Terms of Conditions

22. Cerebrocostomandibular Syndrome - St. Joseph Mercy, Ann Arbor Michigan cerebrocostomandibular syndrome St. Joseph Mercy Health System Hospitals servingAnn Arbor, SE Michigan, Washtenaw County, Livingston County, Wayne County http://www.sjmercyhealth.org/12993.cfm

@import url(default.css); Online Health Information Health Information - Support Groups Back to Health Library Print This Page Email to a Friend Self Help Clearinghouse Cerebrocostomandibular Syndrome Cerebrocostomandibular Syndrome Support Group This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site. Cerebrocostomandibular Syndrome Support Group National network. Founded 1998. Provides support and guidance to families of children with cerebrocostomandibular syndrome (recessed lower mandible and rib anomalies). Exchange of messages through e-mail. Participates in research study. Newsletter. WRITE: Tara Montague 7 Primrose Drive Burlington, NJ 08016 CALL: 609-239-7831 FAX: 609-239-6916 E-MAIL: tmongtague@comcast.net VERIFIED: 4/5/2004 The above information was "verified" as correct on the date at the end of each entry. Since American Self-Help Group Clearinghouse's database is extensive but staffing is limited and information for these organizations can change, it is not possible to keep every entry in American Self-Help Group Clearinghouse database completely current and accurate. Please check with the organizations listed for the most current information.

23. Site Index 24: Saint Joseph Mercy Health System Cerebro Oculo Facio Skeletal Syndrome cerebrocostomandibular syndrome cerebrocostomandibular syndrome Certified diabetes educator (CDE) http://www.sjmercyhealth.org/1024.cfm

@import url(default.css); SITE INDEX 24 previous next Site Index 185: Who is affected by breath-holding spells Site Index 186: Who is affected by insect sting allergies ... Physicians Assistant Residency Program

24. Hill Health Topics A-Z - Cerebrocostomandibular Syndrome Self Help Clearinghouse. cerebrocostomandibular syndrome CerebrocostomandibularSyndrome Support Group. National network. Founded 1998. http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=shc29cbc&S

25. Health Library - cerebrocostomandibular syndrome Support Group. National network. Founded 1998.Provides support and guidance to families of children with http://yalenewhavenhealth.org/library/healthguide/en-us/SelfHelp/topic.asp?hwid=

26. TheFetus.net - Cerebro-costo-mandibular Syndrome -Anupama Patil, MD Definition cerebrocostomandibular syndrome is a potentially lethal developmental Maxillomandibular development in cerebrocostomandibular syndrome. http://www.thefetus.net/page.php?id=410

27. TheFetus.net - Case Of The Week # 34 -Phillip Ramm 117650 cerebrocostomandibular syndrome *166500 OSTEOPATHIA STRIATA WITH CRANIALSCLEROSIS *200600 ACHONDROGENESIS, TYPE IA; ACG1A http://www.thefetus.net/case.php?id=630&answer=1

28. Spine - UserLogin Langer LO, Hermann J. The cerebrocostomandibular syndrome. Cerebrocostomandibularsyndrome Longterm follow-up of a patient and review of the http://www.spinejournal.com/pt/re/spine/fulltext.00007632-199905010-00013.htm

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29. Cerebrocostomandibular Syndrome cerebrocostomandibular syndrome. CCM syndrome Cerebrocosto-mandibular syndrome Departments of Pediatric Imaging and Pathology - Children s Hospital http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=58

30. Developmental And Genetic Diseases CCM syndrome ( cerebrocostomandibular syndrome 1 ) CCMS ( Cerebrocostomandibularsyndrome 1 ) CCNP ( Cataract, nuclear progressive 1 http://www.gfmer.ch/genetic_diseases_v2/index.php?disinit=C

31. Health/Conditions And Diseases/C -- The Doctors Lounge(TM) cerebrocostomandibular syndrome@ 2; Cerebrohepatorenal Syndrome@ 4;Cerebrotendinous Xanthomatosis@ 1; Cervical Cancer@ 21; Cervical Dysplasia@ 7 http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/C/index.cgi

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32. Opera Directory Agnosia Aicardi Syndrome Barth Syndrome cerebrocostomandibular syndrome Kindler Syndrome. An article and case study of this rare disease. http://portal.opera.com/directory/?cat=87697

33. Birth Disorder Information Directory - CA-CL cerebrocostomandibular syndrome. Cerebro costo mandibular syndrome cerebrocostomandibular syndrome. Cerebrohepatorenal Syndrome. See Zellweger Syndrome http://www.bdid.com/defectca.htm

HOME Ca-Cl C Syndrome (Opitz Trigonocephaly Syndrome) C SYNDROME Opitz Trigonocephaly Syndrome Family Network c syndrome C-II Anapolipoproteinemia See Hyperlipoproteinemia, Type Ib CADASIL See Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (Includes Photos) Cafe au lait spots syndrome CAFE-AU-LAIT SPOTS, MULTIPLE Caffey Disease (Infantile Cortical Hyperostosis) List of Sites Cahmr Syndrome (Cataract Hypertrichosis Mental Retardation) cahmr syndrome CAHMR SYNDROME Calcinosis Raynaud Phenomenon with Sclerodactyly and Telangiectasis See CREST Syndrome Calderon Gonzalez Cantu Syndrome (Hair Defect Photosensitivity Mental Retardation) calderon gonzalez cantu syndrome HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION Calloso Genital Dysplasia calloso genital dysplasia Callus Disease Outpatient Clinics in France Calpainopathy See Muscular Dystrophy, Limb-Girdle Type, Type IIa Calvarial Hyperostosis calvarial hyperostosis CALVARIAL HYPEROSTOSIS Camera Lituania Cohen Syndrome (Genes Syndrome, Genoa Syndrome, Holoprosencephaly Craniosynostosis) camera lituania cohen syndrome HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS

34. Smith-Theiler-Schachenmann Syndrome (David W. Smith) (www.whonamedit.com) cerebrocostomandibular syndrome, rib gap defectsmicrognathia syndrome, rib gapdefect with micrognathia. Associated persons Gertrud Dina Schachenmann http://www.whonamedit.com/synd.cfm/1857.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Smith-Theiler-Schachenmann syndrome (David W. Smith) Synonyms: Cerebrocostomandibular syndrome, rib gap defects-micrognathia syndrome, rib gap defect with micrognathia. Associated persons: Gertrud Dina Schachenmann David Weyhe Smith Karl Theiler Description: A developmental disorder affecting both sexes, characterized by severe costovertebral malformations (segmentation of the ribs and fusion of their dorsal ends to the vertebral bodies with a bell-shaped thorax), mental deficiency; and orofacial defects, mainly micrognathia, short hand palate with a central hole, absent soft palate, absent uvula, and glossoptosis. In one case, elbow hypoplasia, defect sacrum and coccyx. In another, webbing of the neck and area of skin redundance. Neonatal respiratory distress and barking cough are frequently observed. Evident from birth. Inheritance is autosomal recessive. Bibliography: D. W. Smith, K. Theiler, G. Schachenmann:

35. Delayed Development Caudal Regression Syndrome; Cerebral Dysplasia; Cerebral Giqantism; Cerebral Palsy;cerebrocostomandibular syndrome; Cerebrohepatorenal Syndrome http://www.rogerknapp.com/medical/eci.htm

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: Screenings and assessments, including hearing and vision. Physical, occupational, speech and language therapy. Activities to develop learning and eating skills. assistive technology. moving on to school or other services as needed at age 3 or when graduating from the program. nutritional services. supporting child care or preschool teachers of enrolled children. ECI services for families: education and counseling.

36. Support Groups Others cerebrocostomandibular syndrome Support Group This is an informal support groupfor families of children with cerebrocostomandibular syndrome (CCMS) http://www.ability.org.uk/support_groups_others.html

"see the ability, not the disability" You to can help support the Ability Project by: Our Aims ... Z Support Groups Others Arizona Family Voices - SHARE Network - Arizona state information, special events, health issues, legislative alerts. S.H.A.R.E. Network; volunteer, sell, or exchange services and equipment for those with special needs. Non-profit, FREE. Aspartame Victims Support Group - Aspartame victims getting off of aspartame and seeing improvements in their health as a result Avandel - Resources explaining a variety of serious medical conditions; understandable explanations of the steps involved in the diagnosis and treatment of catastrophic illnesses. Beryllium Support Group - support group for chronic beryllium disease Better Health Message Boards - LARGE selection of message boards. Burn Survivors Online - Support and information site. Carpal Tunnel Syndrome Message Board Cerebral Palsy Message Board Cerebrocostomandibular Syndrome Support Group - This is an informal support group for families of children with cerebrocostomandibular syndrome (CCMS) 1000 Deaths - A resource site by and for survivors of loved ones' suicides. Support, education, research.

37. UNSW Embryology-OMIM Pierre Robin Syndrome List 23 entries found, searching for pierre robin syndrome 154780 MARSHALLSYNDROME 117650 cerebrocostomandibular syndrome 184840 STICKLER SYNDROME http://embryology.med.unsw.edu.au/OMIMfind/head/OMIM-prs_list.htm

UNSW Embryology HEAD AND NECK DEVELOPMENT Embryology Home Page Select Entries from OMIM Online Mendelian Inheritance in Man (Internet Link) This page is for computers without external internet access. Internet access computers can see the full description of the abnormality from the links below. Back to UNSW Embryology-Head and Neck Notes 23 entries found, searching for "pierre robin syndrome" CATEL-MANZKE SYNDROME WEISSENBACHER-ZWEYMULLER SYNDROME; WZS PIERRE ROBIN SYNDROME PIERRE ROBIN SYNDROME AND OLIGODACTYLY PIERRE ROBIN SYNDROME WITH CONGENITAL HEART MALFORMATION AND CLUBFOOT STICKLER SYNDROME, TYPE I; STL1 MYOPATHY, CONGENITAL NONPROGRESSIVE, WITH MOEBIUS SEQUENCE AND ROBIN SEQUENCE CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE HYALOIDEORETINAL DEGENERATION OF WAGNER VELOCARDIOFACIAL SYNDROME ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES MARSHALL SYNDROME CEREBROCOSTOMANDIBULAR SYNDROME STICKLER SYNDROME, TYPE II; STL2

38. Children Living With Inherited cerebrocostomandibular syndrome. Cerebrotendinous Xanthomatosis. Channelopathy Crigler Najjar Syndrome Type 2. Cushing Disease. Cutanea Tarda Porphyria http://www.climb.org.uk/Disorders/Charlie.htm

Search Our Site C hildren L iving with I nherited M eta b olic Diseases Metabolic Diseases 'C' The National Information and Advice Centre for Metabolic Diseases Disease Also Known as C1 Esterase Inhibitor Deficiency Canavan Leukodystrophy Spongiform Leukodystrophy Carbamyl Phosphate Synthetase Deficiency CPS Carbonic Anhydase II Deficiency Carnitine Deficiency Myopathic/Systemic Carnitine Palmitoyltransferase Deficiency Type 1 CPT-1 Carnosinaemia Carnosinase Deficiency Carotenaemia Central Core Disease Cerebellar Ataxia Cerebellum Hypoplasia Cerebral Calcificat Cerebrocostomandibular Syndrome Cerebrotendinous Xanthomatosis Channelopathy Charcot Marie Tooth Chediak-Higashi Syndrome Childhood Ataxia with Central Hypomyelination Cholesteryl Ester Transfer Protein Deficiency Cholesteryl-Ester Storage Disease Chondrodysplasia Punctata Chorea Acanthocytosis Chronic Progressive External Ophthalmoplegia CPEO Citrullinaemia Cleidocranial Dysplasia Coagulation Factor II Hypoprothrombinemia Cobalamin Disorders Cockayne Syndrome Type 1 Cockayne Syndrome Type 2 Cockayne Syndrome Type 3 Coffin Lowry Syndrome Coffinsiris Cohen Syndrome Collagen Disorders Combined Deficiencies of Adenosyl-Cobalamin and Methyl-Cobalamin Combined Pituitary Hormone Deficiency Congenital Adrenal Hyperplasia – 3 Beta Hydroxy-Steroid Dehydrogenase Congenital Adrenal Hyperplasia CAH Congenital Adrenal Hyperplasia – 11 Beta Hydroxylase Deficiency CAH Congenital Adrenal Hyperplasia – 17 Alpha Hydroxylase Deficiency

39. A Listing Of Disorders Cerebro Oculo Facio Skeletal Syndrome. cerebrocostomandibular syndrome.Chandler s Syndrome. Charcot Marie Tooth Disease. CHARGE Association http://medschool.umaryland.edu/BTBank/Family/Disorders_C.htm

Brain and Tissue Bank 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

40. Health Library - 12.31.13.113/library/healthguide/enus/illnesscond titanium_rib_project Jarcho-Levin Syndrome (spondylocostal dysplasia), Pierre-Robin Syndrome,cerebrocostomandibular syndrome, Golden-Har Syndrome, and others. http://12.42.224.150/library/healthguide/en-us/SelfHelp/topic.asp?hwid=shc29cbc

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