Overview
Dentin dysplasia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Research Evidence
Peer-reviewed studies linked via MeSH term "Dysplasia, Dentin" from the MEDLINE/PubMed database.
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A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies.
[object Object], [object Object], [object Object] et al. · Oral Dis · 2023
PMID: 36597617Review
Dentin dysplasia type I-A dental disease with genetic heterogeneity.
[object Object], [object Object], [object Object] et al. · Oral Dis · 2019
Dental Management of Heritable Dental Developmental Anomalies.
Pediatr Dent · 2017
PMID: 29179374Review
Guideline on Dental Management of Heritable Dental Developmental Anomalies.
Pediatr Dent · 2016
PMID: 27931469Review
The fine tuning role of microRNA-RNA interaction in odontoblast differentiation and disease.
[object Object], [object Object], [object Object] · Oral Dis · 2015
PMID: 24654877Review
Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification.
[object Object], [object Object], [object Object] · Eur J Hum Genet · 2015
An overview of molecular and genetic alterations in selected benign odontogenic disorders.
[object Object] · Arch Pathol Lab Med · 2014
PMID: 24878015Review
Hereditary dentine diseases resulting from mutations in DSPP gene.
[object Object], [object Object] · J Dent · 2012
PMID: 22521702Review
[Dentinogenesis imperfecta: a developmental anomaly of the dentin in the primary dentition. A literature review].
[object Object] · Refuat Hapeh Vehashinayim (1993) · 2010
PMID: 20597260Review
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.
[object Object], [object Object], [object Object] et al. · Orphanet J Rare Dis · 2008
Search all PubMed articles for Dentin dysplasia
Research data from MEDLINE/PubMed
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Defective tooth enamel
Very frequent (80-99%)HP:0000682
Increased bone mineral density
Very frequent (80-99%)HP:0011001
Misshapened teeth
Very frequent (80-99%)HP:0006482
Formation of new noncancerous bone on top of existing bone
Frequent (30-79%)HP:0100777
Related Conditions
Dentin dysplasia, type I(child)
Dentin dysplasia with sclerotic bone syndrome(child)
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency(child)
Shell teeth(child)
Dentin dysplasia, type II(child)
Teeth hard tissue diseases(parent)
Congenital anomaly of tooth(parent)
Oral lesion(parent)
Hereditary disorder of tooth(parent)
Developmental hereditary disorder(parent)
Autosomal dominant hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 109492001
- UMLS CUI
- C0011430
- Fully Specified Name
- Dentin dysplasia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 4
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.