Extractions: Cleidocranial Dysplasia is a rare craniofacial disorder inherited as an autosomal dominant trait. Major symptoms may include premature closing of the soft spot on the head (coronal), delayed closure of the space between the bones of the skull (fontanels) and complete or partial absence of the collarbones (clavicles).
Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Cleidocranial dysplasia is a rare skeletal dysplasia characterized by short stature, distinctive facial features and narrow, sloping shoulders caused by defective or absent collarbones (clavicles). Major symptoms may include premature closing of the soft spot on the head (coronal), delayed closure of the space between the bones of the skull (fontanels), narrow and abnormally shaped pelvic and pubic bones and deformations in the chest (thoracic region). Delayed eruption of teeth, moderately short stature, a high arched palate, a wide pelvic joint, failure of the lower jaw joints to unite, and fingers that are irregular in length may also be present. Cleidocranial dysplasia is inherited as an autosomal dominant genetic trait. Children's Craniofacial Association
Healthcyclopedia Index - M Marfan Syndrome. mariesainton disease. Marinesco-Sjogren Syndrome. Master's Disease. Mayer Rokitansky Kuster Hauser Syndrome. McArdle's Disease. Measles, German http://www.healthcyclopedia.com/m.html
Extractions: Cleidocranial dysplasia is a rare skeletal dysplasia characterized by short stature, distinctive facial features and narrow, sloping shoulders caused by defective or absent collarbones (clavicles). Major symptoms may include premature closing of the soft spot on the head (coronal), delayed closure of the space between the bones of the skull (fontanels), narrow and abnormally shaped pelvic and pubic bones and deformations in the chest (thoracic region). Delayed eruption of teeth, moderately short stature, a high arched palate, a wide pelvic joint, failure of the lower jaw joints to unite, and fingers that are irregular in length may also be present. Cleidocranial dysplasia is inherited as an autosomal dominant genetic trait.
Index Ptosis (with jawwinking) Marden Walker Syndrome Mareo Marfan Syndrome MarfanoidHypermobility Syndrome Marie Disease marie-sainton disease Marinesco Sjogren http://my.webmd.com/hw/index/index-topics-M.asp
Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Information on the following diseases can be found in the Related Disorders section of this report: Cleidocranial dysplasia is a rare skeletal dysplasia characterized by short stature, distinctive facial features and narrow, sloping shoulders caused by defective or absent collarbones (clavicles). Major symptoms may include premature closing of the soft spot on the head (coronal), delayed closure of the space between the bones of the skull (fontanels), narrow and abnormally shaped pelvic and pubic bones and deformations in the chest (thoracic region). Delayed eruption of teeth, moderately short stature, a high arched palate, a wide pelvic joint, failure of the lower jaw joints to unite, and fingers that are irregular in length may also be present. Cleidocranial dysplasia is inherited as an autosomal dominant genetic trait.
Health Topics Top. Marie Disease. mariesainton disease. Marinesco Sjogren Syndrome. Marinesco-GarlandSyndrome. Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism. http://www.bchealthguide.org/kbase/list/ht/m.htm
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Cleidocranial Dysplasia Dysplasia (cleido = collar bone, + cranial = head, + dysplasia = abnormal forming), also known as Cleidocranial Dysostosis and mariesainton disease, is a http://www.faces-cranio.org/Disord/CCD.htm
Extractions: Cleidocranial Dysplasia ( cleido = collar bone, + cranial = head, + dysplasia = abnormal forming) , also known as Cleidocranial Dysostosis and Marie-Sainton Disease, is a condition characterized by defective development of the cranial bones and by the complete or partial absence of the collar bones (clavicles). Characteristics include: Delayed closure (ossification) of the space between the bones of the skull (fontanels) Premature closing of the coronal suture Protruding jaw (mandible) and protruding brow bone (frontal bossing) Wide nasal bridge due to increased space between the eyes (hypertelorism) High arched palate or possible cleft palate Short stature Scoliosis of the spine There is no link between anything the mother did or did not do while she was pregnant and the occurrence of Cleidocranial Dysplasia. It is transmitted as an autosomal dominant trait. The cause is not yet known, but several chromosome abnormalities have been linked with this syndrome, including chromosome 6p21.
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Entrez PubMed No abstract, Cleidocranial dysostosis (Pierre mariesainton disease)Acta Stomatol Belg. 1976;73(2)163-71. French. No abstract available. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Display&dopt=pubmed_
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NORD - National Organization For Rare Disorders, Inc. Dysplasia, Cleidocranial; Dysplasia, Osteodental; mariesainton disease.Disorder Subdivisions General Discussion Cleidocranial dysplasia http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Cleidocranial
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