Maxillofacial dysostosis

Common Name(s)

Maxillofacial dysostosis

Description for this condition is not yet available.
 

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Condition Specific Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Maxillofacial dysostosis" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Maxillofacial dysostosis" returned 1 free, full-text research articles on human participants. First 3 results:

Maxillofacial dysostosis.
 

Author(s): V Escobar, J Eastman, D Weaver, M Melnick

Journal: J. Med. Genet.. 1977 Oct;14(5):355-8.

 

Four individuals in a single family affected with maxillofacial dysostosis are reported. Maxillary hypoplasia, delayed onset of speech, and poor development of language skills without associated hearing loss are the main characteristics of the syndrome which is transmitted as an autosomal ...

Last Updated: 23 Feb 1978

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Maxillofacial dysostosis" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Survey Study and Records Review of Treatment Outcomes in Freeman-Sheldon Syndrome
 

Status: Recruiting

Condition Summary: Freeman-Sheldon Syndrome; Arthrogryposis Distal Type 2A; Whistling Face Syndrome; Craniocarpotarsal Dysplasia; Craniocarpotarsal Dystrophy; Freeman-Sheldon Syndrome Variant; Sheldon-Hall Syndrome; Arthrogryposis Distal Type 2B; Gordon Syndrome; Arthrogryposis Distal Type 3; Arthrogryposis Distal Type 1; Arthrogryposis, Distal, Type 1A; Arthrogryposis Distal Type 1B; Arthrogryposis, Distal; Craniofacial Abnormalities; Arthrogryposis

 

Last Updated: 5 Apr 2017

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Natural History of Craniofacial Anomalies and Developmental Growth Variants
 

Status: Recruiting

Condition Summary: Prognathism; Dentofacial Deformities; Hemifacial Macrosomia; Craniofacial Microsomia

 

Last Updated: 26 Oct 2017

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Bohring-Opitz Syndrome and ASXL Registry
 

Status: Recruiting

Condition Summary: Bohring-Opitz Syndrome; ASXL1 Gene Mutation; Shashi-Pena Syndrome; ASXL2 Gene Mutation; Bainbridge-Ropers Syndrome; ASXL3 Gene Mutation

 

Last Updated: 5 Oct 2017

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