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Abnormality of dental enamel

Known as: Enamel abnormalities, Malformation of tooth enamel, Malformation of dental enamel 
An abnormality of the dental enamel. [HPO:probinson]
National Institutes of Health

Related topics

Related topics

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Arthrogryposis and ectodermal dysplasia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Comparing tooth enamel disturbances in a pediatric population that had received prior chemotherapy treatment to age-matched controls from the Virginia Commonwealth University Pediatric Dentistry…
COMPARING TOOTH ENAMEL DISTURBANCES IN A PEDIATRIC POPULATION THAT HAD RECEIVED PRIOR CHEMOTHERAPY TREATMENT TO AGE-MATCHED… 
Review
2013
Review
2013
Molecular mechanisms of renal and extrarenal manifestations caused by inactivation of the electrogenic Na+-HCO3− cotransporter NBCe1
The electrogenic Na+-HCO3− cotransporter NBCe1 plays an essential role in bicarbonate absorption from renal proximal tubules, but… 
2013
2013
15-year follow-up of a case of amelogenesis imperfecta: importance of psychological aspect and impact on quality of life
Amelogenesis imperfecta (AI) represents a group of hereditary conditions which affects enamel formation in the primary and… 
2012
2012
Epithelial and Mesenchymal Cell Biology Type VII Collagen Deficiency Causes Defective Tooth Enamel Formation due to Poor Differentiation of Ameloblasts
From the Departments of Dermatology,* Hokkaido University Graduate School of Medicine, Sapporo, Japan; the Departments of Oral… 
2012
2012
Palmoplantar keratoderma with growth hormone deficiency
Abstract Palmoplantar keratoderma (PPK) is a diverse group of disorders, characterized by thickening of the palms and soles… 
2010
2010
Fourth case of cerebral, ocular, dental, auricular, skeletal syndrome (CODAS), description of new features and molecular analysis
Cerebral, ocular, dental, auricular, skeletal syndrome (CODAS, OMIM 600373) is a very rare congenital malformation syndrome. This… 
2008
2008
Serum vitamin A and carotene levels in Down's syndrome and other retarded subjects showing enamel abnormalities of the permanent dentition.
2004
2004
Amelogenesis Imperfecta in a New Animal Model—a Mutation in Chromosome 5 (human 4q21)
Candidate genes for amelogenesis imperfecta (AI) and dentinogenesis imperfecta (DI) are located on 4q21 in humans. We tested our… 
2001
2001
Normal expression of the 19‐DEJ‐1 epitope in two siblings with late‐onset junctional epidermolysis bullosa
We describe two siblings with late‐onset junctional epidermolysis bullosa (JEB) (formerly called epidermolysis junctionalis… 
1985
1985
Prevalence of gestational and perinatal insults in brain-damaged children.
The value of utilizing the analysis of unusual dermatoglyphic patterns and of microscopic dental enamel abnormalities as… 
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