Literature DB >> 9799305

Otodental syndrome, oculo-facio-cardio-dental (OFCD) syndrome, and lobodontia: dental disorders of interest to the pediatric radiologist.

R J Gorlin1.   

Abstract

Three unusual dental anomalies are presented which should be of interest to the pediatric radiologist: otodental syndrome - an autosomal dominant syndrome of bizarre, greatly enlarged teeth with bulbous crowns (globodontia) that spares the incisors, in combination with sensorineural hearing loss; oculo-facio-cardio-dental syndrome - an X-linked dominant syndrome that is lethal in males, characterized by congenital cataracts, unusual facies, atrial septal defect (ASD), ventricular septal defect (VSD), and canine teeth that cease to grow only when they cut off their own blood supply by growing through the orbit and lower border of mandible; and lobodontia - a dominant disorder characterized by teeth whose crowns resemble those of a wolf.

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Mesh:

Year:  1998        PMID: 9799305     DOI: 10.1007/s002470050469

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  7 in total

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2.  A genome-wide linkage scan for quantitative trait loci influencing the craniofacial complex in humans (Homo sapiens sapiens).

Authors:  Richard J Sherwood; Dana L Duren; Michael C Mahaney; John Blangero; Thomas D Dyer; Shelley A Cole; Stefan A Czerwinski; Wm Cameron Chumlea; Roger M Siervogel; Audrey C Choh; Ramzi W Nahhas; Miryoung Lee; Bradford Towne
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3.  Dental abnormalities in individuals with pathogenic germline variation in DICER1.

Authors:  Sooji Choi; Janice S Lee; Carol W Bassim; Harvey Kushner; Ann G Carr; Pamela J Gardner; Laura A Harney; Kris Ann P Schultz; Douglas R Stewart
Journal:  Am J Med Genet A       Date:  2019-07-16       Impact factor: 2.802

4.  Molecular characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl.

Authors:  Yong-hui Jiang; Ping Fang; Adekunle M Adesina; Patricia Furman; Jennifer J Johnston; Leslie G Biesecker; Chester W Brown
Journal:  Am J Med Genet A       Date:  2009-06       Impact factor: 2.802

5.  Detecting genetic association of common human facial morphological variation using high density 3D image registration.

Authors:  Shouneng Peng; Jingze Tan; Sile Hu; Hang Zhou; Jing Guo; Li Jin; Kun Tang
Journal:  PLoS Comput Biol       Date:  2013-12-05       Impact factor: 4.475

Review 6.  Genetic Syndromes Associated with Congenital Cardiac Defects and Ophthalmologic Changes - Systematization for Diagnosis in the Clinical Practice.

Authors:  Priscila H A Oliveira; Beatriz S Souza; Eimi N Pacheco; Michele S Menegazzo; Ivan S Corrêa; Paulo R G Zen; Rafael F M Rosa; Claudia C Cesa; Lucia C Pellanda; Manuel A P Vilela
Journal:  Arq Bras Cardiol       Date:  2018-01       Impact factor: 2.000

7.  Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Authors:  Virginie Laugel-Haushalter; Supawich Morkmued; Corinne Stoetzel; Véronique Geoffroy; Jean Muller; Anne Boland; Jean-François Deleuze; Kirsley Chennen; Waranuch Pitiphat; Hélène Dollfus; Karen Niederreither; Agnès Bloch-Zupan; Patimaporn Pungchanchaikul
Journal:  Front Physiol       Date:  2018-09-26       Impact factor: 4.566

  7 in total

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