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… (More)
National Institutes of Health

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Narrower (16)

ADULT SYNDROMEAloi Tomasini Isaia syndromeAnodontia of Permanent DentitionDeafness oligodontia syndrome
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Acrootoocular SyndromeBrachymetapody-Anodontia-Hypotrichosis-AlbinoidismCongenital absenceCranioectodermal Dysplasia
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Broader (1)

Congenital Disorders

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
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… (More)
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Highly Cited
2011
Highly Cited
2011
Prevalence and distribution of selected developmental dental anomalies in an Indian population.
The purpose of this study was to determine the prevalence of developmental dental anomalies in an Indian population and to… (More)
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2008
2008
External apical root resorption in patients treated with conventional and self-ligating brackets.
INTRODUCTION Our aim was to comparatively investigate the amount of external apical root resorption (EARR) between conventional… (More)
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2006
2006
Prosthodontic and psychological factors in treating patients with congenital and craniofacial defects.
This article addresses treatment of patients with various types of congenital defects, including partial and total anodontia… (More)
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Highly Cited
2005
Highly Cited
2005
Early prosthetic treatment of patients with ectodermal dysplasia: a clinical report.
Hypohidrotic ectodermal dysplasia is a hereditary disorder of ectodermal origin. The early orthodontic treatment of 2 young boys… (More)
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2005
2005
Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2).
Kallmann syndrome (KAL) combines hypogonadotropic hypogonadism and anosmia. Hypogonadism is due to Gonadotropin Releasing Hormone… (More)
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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… (More)
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Highly Cited
2004
Highly Cited
2004
MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.
In this study, we sought to determine the association between tooth agenesis and DNA sequence variation in the genes MSX1 and… (More)
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1998
1998
Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome.
Axenfeld-Rieger syndrome (ARS) and iridogoniodysgenesis syndrome (IGDS) are clinically related autosomal dominant disorders which… (More)
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1997
1997
Use of endosseous implants in a 3-year-old child with ectodermal dysplasia: case report and 5-year follow-up.
The ectodermal dysplasias represent a group of inherited disorders characterized by defects in tissues that are derived from… (More)
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