SLCentral Directory - Health - Conditions And Diseases - C Palsy@ (143); cerebrocostomandibular syndrome@ (2); CerebrohepatorenalSyndrome@ (5); Cerebrotendinous Xanthomatosis@ (1); Cervical http://www.slcentral.com/directory/index.php/Health/Conditions_and_Diseases/C/
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Annotate Technologies cerebrocostomandibular syndrome Support Group This is an informal support groupfor families of children with cerebrocostomandibular syndrome (CCMS). http://www.annotate.net/html/Annotate_Directory/Top/Health/Conditions_&_Diseases
PhatNav Directory - Health/Conditions_and_Diseases/R Health/Conditions and Diseases/Rare Disorders/cerebrocostomandibular syndrome.Health/Conditions and Diseases/Infectious Diseases/Fungal/Ringworm. http://www.phatnav.com/directory/Health/Conditions_and_Diseases/R.cat
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Extractions: Syndrome cerebrocostomandibular (CCM) syndrome (CCMS) Synonyms Smith-Theiler-Schachenmann syndrome rib-gap syndrome rib gap defect-micrognathia syndrome Summary Mental retardation associated mainly with costovertebral malformations and orofacial defects. Mental defect may not be inherent but rather a consequence of neonatal respiratory distress. Major Features Head and neck: Microcephaly and micrognathia. Mouth and oral structures: Palatal defects include short hard palate, absent soft palate, cleft palate, and absent uvula in association with glossoptosis. Neck: Pterygium colli. Thorax: Bilateral rib gaps between the costovertebral junction area and he lateral arc, most frequently occurring between the third and seventh thoracic segments occur in most cases. Flail chest is the usual consequence. Hypoplasia of the sternum and clavicles may be associated. Extremities: Elbow hypoplasia and other limb abnormalities may occur. Spine: Fusion of the vertebrae to each other, scoliosis, and hemivertebrae may be associated.
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A Listing Of Disorders Cerebral Palsy. Cerebro Oculo Facio Skeletal syndrome. Cerebrocostomandibularsyndrome. Chandler s syndrome. Charcot Marie Tooth Disease. CHARGE Association. http://medschool.umaryland.edu/BTBank/Family/Disorders_C.htm
PHP-Nuke Canada Site - Links Dysplasia Support Online For those seeking support and information concerning therare bone diseases fibrous dysplasia, McCune Albright syndrome and Cherubism http://www.phpnuke-ca.com/Links-Health__Conditions_and_Diseases__Rare_Disorders_
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PHP-Nuke Canada Site - Links http//www.geneclinics.org Blepharophimosis Ptosis Epicanthus Inversus syndrome TheBPEI (BPES) Family Network encourages people to get in touch with each other http://www.phpnuke-ca.com/Links-Health__Conditions_and_Diseases__Genetic_Disorde
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/Genetic_Disorders/
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Extractions: Health Conditions and Diseases Rare Disorders Go to Directory Home Web Pages - ranked by popularity National Library of Medicine: cerebrocostomandibular (CCM) syndrome (CCMS) http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome098.html A list of synonyms, summary and major features. NORD - Cerebrocostomandibular Syndrome http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Cerebrocostomandibular%20Syndrome Sample report, plus links to organisations. [Fee required for full report]
Children Living With Inherited Cerebellum Hypoplasia. Cerebral Calcificat. Cerebral Palsy. CerebrocostomandibularSyndrome. Cerebrotendinous Xanthomatosis. Channelopathy. Charcot Marie Tooth. http://www.climb.org.uk/Disorders/Charlie.htm
Extractions: 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 Carbohydrate Deficient Glycoprotein Syndrome General/Undiagnosed Congenital Disorders of Glycosylation Carbohydrate Deficient Glycoprotein Syndrome Phosphomannomutase Deficiency Carbohydrate Deficient Glycoprotein Syndrome Phosphomannose Isomerase Deficiency Carbohydrate Deficient Glycoprotein Syndrome Glucosyltransferase-I Deficiency Carbohydrate Deficient Glycoprotein Syndrome N- Acetylglucosaminyltransferase II Deficiency Carbonic Anhydase II Deficiency Carnitine Deficiency Myopathic Carnitine Deficiency Systemic Carnitine Palmitoyltransferase CPT-1 Carnitine Palmitoyltransferase CPT-2 Carnosinaemia Carnosinase Deficiency Carotenaemia Central Core Disease Cerebellar Ataxia Cerebellum Hypoplasia Cerebral Calcificat Cerebral Palsy 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
