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Anodontia of Permanent Dentition
Known as:
Teeth, Permanent, Absence of
, Absent permanent teeth
, Failure of development of secondary teeth
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A congenital defect characterized by the absence of one or more permanent teeth, including oligodontia, hypodontia, and adontia of the of permanent…
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National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Developmental absence of tooth
Johanson-Blizzard syndrome
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population
D. Grejtakova
,
D. Gabrikova-Dojcakova
,
+6 authors
J. Bernasovska
Journal Genetika
2018
Corpus ID: 53079080
Nonsyndromic hypodontia is a congenital absence of less than six permanent teeth, with a most common subtype maxillary lateral…
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2014
2014
Cleidocranial Dysplasia with Autosomal Dominant Inheritance Pattern
Puneet Bhargava
,
Saba Khan
,
Rohit Sharma
,
S. Bhargava
Annals of Medical and Health Sciences Research
2014
Corpus ID: 27386578
Cleidocranial dysplasia (CCD) is an autosomal dominant disease with a wide range of expression, characterized by clavicular…
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Review
2011
Review
2011
Hallermann-Streiff syndrome: case report and literature review.
Peter Robotta
,
Edgar Schafer
Quintessence International
2011
Corpus ID: 45850608
Hallermann-Streiff syndrome is a rare genetic disorder characterized primarily by head and face abnormalities. Patients show…
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2006
2006
Increased hypodontia through the twentieth century
C. Flores‐Mir
Evidence-Based Dentistry
2006
Corpus ID: 11794965
Data sourcesPubMed provided the primary data source and was supplemented by a manual search of reference lists from relevant…
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2002
2002
Mutational Analysis of Families Affected with Molar Oligodontia
S. Frazier-Bowers
,
Meredith R Scott
,
A. Cavender
,
J. Mensah
,
R. D'Souza
Connective Tissue Research
2002
Corpus ID: 22185229
Oligodontia, the congenital absence of six or more permanent teeth, is a common developmental anomaly of human dentition whose…
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2000
2000
Congenital absence of permanent teeth in a six-generation Chinese kindred.
H. Wang
,
S. Zhao
,
+6 authors
L. He
American journal of medical genetics
2000
Corpus ID: 23835881
We report on rare, heritable, permanent tooth agenesis in a large Chinese kindred. The congenital absence of permanent teeth…
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1994
1994
Hallerman-Streiff syndrome: case report and recommendations for dental care.
M. D. da Fonseca
,
W. Mueller
ASDC journal of dentistry for children
1994
Corpus ID: 9142116
Hallerman-Streiff syndrome is a rare congenital anomaly characterized by a peculiar bird facies, mandibular and maxillary…
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1993
1993
A case of Johanson‐Blizzard syndrome complicated by diabetes mellitus
K. Nagashima
,
H. Yagi
,
T. Kuroume
Clinical Genetics
1993
Corpus ID: 33408299
We report a girl with Johanson‐Blizzard syndrome complicated by diabetes mellitus. She presented several characteristic…
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1992
1992
Microdontia, hypodontia, short bulbous roots and root canals with strabismus, short stature, and borderline mentality.
E. Bazopoulou‐Kyrkanidou
,
C. Dacou-voutetakis
,
H. Nassi
,
K. Tosios
,
S. Kyrkanides
,
M. Damoli
Oral surgery, oral medicine, and oral pathology
1992
Corpus ID: 37841968
1983
1983
Occlusal anomalies in Finnish students related to age, sex, absent permanent teeth and orthodontic treatment.
T. Laine
,
H. Hausen
European Journal of Orthodontics
1983
Corpus ID: 34503415
Occlusal anomalies in 451 Finnish undergraduates were recorded. Details of previous orthodontic treatment were obtained from a…
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