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Hypodontia
Known as:
Congenital partial absence of teeth
, Partial absence of teeth
, Oligodontia
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A developmental anomaly characterized by a reduced number of teeth, whereby up to 6 teeth are missing. [HPO:ibailleulforestier]
National Institutes of Health
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ADULT SYNDROME
AXENFELD-RIEGER SYNDROME, TYPE 3
Aarskog syndrome
Adult junctional epidermolysis bullosa (disorder)
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
A novel missense mutation in the paired domain of human PAX9 causes oligodontia
Ji-lin Zhao
,
Q. Hu
,
Yang-xi Chen
,
S. Luo
,
L. Bao
,
Yue Xu
American Journal of Medical Genetics. Part A
2007
Corpus ID: 23338922
PAX9 and MSX1 are transcription factors that play essential roles in craniofacial and limb development. In humans, mutations in…
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Highly Cited
2005
Highly Cited
2005
Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia.
R. Kist
,
Michelle Watson
,
+4 authors
H. Peters
Human Molecular Genetics
2005
Corpus ID: 27881494
Missing teeth (hypodontia and oligodontia) are a common developmental abnormality in humans and heterozygous mutations of PAX9…
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Highly Cited
2005
Highly Cited
2005
Maxillary canine anomalies and tooth agenesis.
S. Camilleri
European Journal of Orthodontics
2005
Corpus ID: 10926734
The aims of the study were to analyse the records of 26 subjects (18 females, eight males) with maxillary canine-first premolar…
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Highly Cited
2005
Highly Cited
2005
Skeletal Class III oligodontia patient treated with titanium screw anchorage and orthognathic surgery.
S. Kuroda
,
Yasuyo Sugawara
,
K. Yamashita
,
T. Mano
,
T. Takano-Yamamoto
American Journal of Orthodontics and Dentofacial…
2005
Corpus ID: 30262718
2005
2005
Hypohidrotic ectodermal dysplasia with bilateral impacted teeth at the coronoid process: a case rehabilitated with mini dental implants.
N. Güler
,
S. Cildir
,
Ufuk Işeri
,
N. Sandalli
,
O. Dilek
Oral surgery, oral medicine, oral pathology, oral…
2005
Corpus ID: 13141107
2003
2003
Leukodystrophy associated with oligodontia in a large inbred family: Fortuitous association or new entity?
S. Atrouni
,
Antoine Darazé
,
J. Tamraz
,
A. Cassia
,
C. Caillaud
,
A. Mégarbané
American Journal of Medical Genetics. Part A
2003
Corpus ID: 1653310
We describe a large inbred Syrian pedigree with an autosomal recessive neurodegenerative disorder. The clinical picture of the…
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Highly Cited
2000
Highly Cited
2000
Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia.
Raquel Mantuaneli Scarel
,
P. Trevilatto
,
Oswaldo Di Hiplito
,
L. Camargo
,
S. Line
American journal of medical genetics
2000
Corpus ID: 20826086
Hypodontia, the congenital absence of one or a few permanent teeth, is one of the most frequent alterations of the human…
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Highly Cited
1988
Highly Cited
1988
Comparison of dental findings in patients with isolated growth hormone deficiency treated with human growth hormone (hGH) and in untreated patients with Laron-type dwarfism.
H. Sarnat
,
I. Kaplan
,
A. Pertzelan
,
Z. Laron,
Oral surgery, oral medicine, and oral pathology
1988
Corpus ID: 35024209
1985
1985
Expression of X‐linked hypohidrotic ectodermal dysplasia in six males and in their mothers
A. Söderholm
,
I. Kaitila
Clinical Genetics
1985
Corpus ID: 10676410
Six male patients with confirmed X‐linked hypohidrotic ectodermal dysplasia and their mothers were studied to determine the…
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Highly Cited
1983
Highly Cited
1983
Hypodontia and delayed development of the second premolars in cleft palate children.
R. Ranta
European Journal of Orthodontics
1983
Corpus ID: 42378868
Bilateral asymmetry of congenitally absent second premolars, the rate of tooth formation of the remaining second premolars and…
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