| Autosomal dominant transmission of ankylosed teeth, abnormalities of the jaws, and clinodactyly. A four-generation study. | |
| | |
MedLine Citation:
|
PMID: 4006275 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
Twelve persons in four generations of a rural family of mixed racial ancestry exhibited ankylosed teeth, bilateral clinodactyly of the fifth fingers, and abnormalities of the jaws. This previously undescribed association of dental, digital, and skeletal anomalies appears to be transmitted in an autosomal dominant manner in this family. Clinical manifestations in the examined persons and an extended family history are described in detail. Previous studies of apparently hereditary dental ankylosis are similarly discussed. |
| | |
Authors:
|
M Z Pelias; M C Kinnebrew |
Related Documents
:
|
11066715 - Key steps in the strategic analysis of a dental practice. 10174785 - Managing the strategic capital cycle. 9567575 - Uses of mushrooms by finns and karelians. 22309875 - Financial management practices and attitudes of dental hygienists: a descriptive study. 3380965 - Radiologic evaluation of mass casualty victims: lessons from the gander, newfoundland, ... 22486535 - The dental occlusion as a suspected cause for tmds: epidemiological and etiological con... |
Publication Detail:
|
Type: Case Reports; Journal Article |
Journal Detail:
|
Title: Clinical genetics Volume: 27 ISSN: 0009-9163 ISO Abbreviation: Clin. Genet. Publication Date: 1985 May |
Date Detail:
|
Created Date: 1985-08-22 Completed Date: 1985-08-22 Revised Date: 2004-11-17 |
Medline Journal Info:
|
Nlm Unique ID: 0253664 Medline TA: Clin Genet Country: DENMARK |
Other Details:
|
Languages: eng Pagination: 496-500 Citation Subset: IM |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Adult Female Fingers / abnormalities* Genes, Dominant* Humans Jaw Abnormalities / genetics* Male Pedigree Syndrome Tooth Abnormalities / genetics* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Unbalanced karyotype with normal phenotype in a family with translocation (8;13)(p21;q22).
Next Document: Centromeric instability of chromosomes 1 and 16 with variable immune deficiency: a new syndrome.