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Developmental absence of tooth

Known as: Complete anodontia, Complete absence of teeth, Anodontia 
Congenital absence of the teeth; it may involve all (total anodontia) or only some of the teeth (partial anodontia, hypodontia), and both the… 
National Institutes of Health

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Narrower (17)

ADULT SYNDROMEAloi Tomasini Isaia syndromeAnodontia of Permanent DentitionCleft Palate, Deafness, and Oligodontia
Acrootoocular SyndromeBrachymetapody-Anodontia-Hypotrichosis-AlbinoidismCongenital absenceCranioectodermal Dysplasia

Broader (1)

Congenital Disorders

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes.
CONTEXT The complexity of genetic testing in Kallmann syndrome (KS) is growing and costly. Thus, it is important to leverage the… 
Highly Cited
2012
Highly Cited
2012
Mutations in WNT10A are present in more than half of isolated hypodontia cases
Background Dental agenesis is the most common, often heritable, developmental anomaly in humans. Mutations in MSX1, PAX9, AXIN2… 
Review
2009
Review
2009
Dental agenesis: genetic and clinical perspectives.
Dental agenesis is the most common developmental anomaly in humans and is frequently associated with several other oral… 
Review
2008
Review
2008
The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders.
Highly Cited
2008
Highly Cited
2008
External apical root resorption in patients treated with conventional and self-ligating brackets.
Highly Cited
2004
Highly Cited
2004
A meta-analysis of the prevalence of dental agenesis of permanent teeth.
OBJECTIVE: To gain more insight into the prevalence of dental agenesis. METHODS: Data from Caucasian populations in North America… 
Highly Cited
2004
Highly Cited
2004
Dental pathology; epidemiology: A meta-analysis of the prevalence of dental agenesis of permanent teeth
Dental agenesis appears more prevalent in Europe and Australia than in North American Caucasians, and higher in females than… 
Highly Cited
2004
Highly Cited
2004
Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.
We report on the clinical and molecular findings in 25 males and three females with Kallmann syndrome (KS) aged 10-53 yr. Ten… 
Highly Cited
2001
Highly Cited
2001
Orthodontic aspects of the use of oral implants in adolescents: a 10-year follow-up study.
The aim of the present study was to evaluate the long-term effect of implants installed in different dental areas in adolescents… 
Highly Cited
1994
Highly Cited
1994
Osseointegrated implants in adolescents. An alternative in replacing missing teeth?
In 15 adolescents (13 years 2 months-19 years 4 months) in the late dental stage, Brånemark implants (n = 27) were chosen to… 
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