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Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report

Amelogenesis imperfecta (AI) is a group of hereditary disorders that affect the quality and/or quantity of dental enamel. This paper describes the clinicopathological features of a patient who was born of nonconsanguineous parents and who presented with oral alterations, including yellow and misshap...

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Autores principales: Patel, Alok, Jagtap, Chetana, Bhat, Chetan, Shah, Rohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456756/
https://www.ncbi.nlm.nih.gov/pubmed/26097369
http://dx.doi.org/10.4103/0976-237X.156063
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author Patel, Alok
Jagtap, Chetana
Bhat, Chetan
Shah, Rohan
author_facet Patel, Alok
Jagtap, Chetana
Bhat, Chetan
Shah, Rohan
author_sort Patel, Alok
collection PubMed
description Amelogenesis imperfecta (AI) is a group of hereditary disorders that affect the quality and/or quantity of dental enamel. This paper describes the clinicopathological features of a patient who was born of nonconsanguineous parents and who presented with oral alterations, including yellow and misshapen teeth, intrapulpal calcifications, delayed tooth eruption, and gum enlargement. Scanning electron microscopy of the teeth revealed hypoplastic enamel, and a renal ultrasound detected bilateral nephrocalcinosis, leading to a diagnosis of AI and nephrocalcinosis syndrome. Since nephrocalcinosis is often asymptomatic and can be associated with impaired renal function, dentists who see children with a generalized and thin hypoplastic AI should consider a renal ultrasound scan and referral to a Nephrologist. Children with nephrocalcinosis should also be considered for a dental check.
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spelling pubmed-44567562015-06-19 Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report Patel, Alok Jagtap, Chetana Bhat, Chetan Shah, Rohan Contemp Clin Dent Case Report Amelogenesis imperfecta (AI) is a group of hereditary disorders that affect the quality and/or quantity of dental enamel. This paper describes the clinicopathological features of a patient who was born of nonconsanguineous parents and who presented with oral alterations, including yellow and misshapen teeth, intrapulpal calcifications, delayed tooth eruption, and gum enlargement. Scanning electron microscopy of the teeth revealed hypoplastic enamel, and a renal ultrasound detected bilateral nephrocalcinosis, leading to a diagnosis of AI and nephrocalcinosis syndrome. Since nephrocalcinosis is often asymptomatic and can be associated with impaired renal function, dentists who see children with a generalized and thin hypoplastic AI should consider a renal ultrasound scan and referral to a Nephrologist. Children with nephrocalcinosis should also be considered for a dental check. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4456756/ /pubmed/26097369 http://dx.doi.org/10.4103/0976-237X.156063 Text en Copyright: © Contemporary Clinical Dentistry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Patel, Alok
Jagtap, Chetana
Bhat, Chetan
Shah, Rohan
Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report
title Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report
title_full Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report
title_fullStr Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report
title_full_unstemmed Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report
title_short Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report
title_sort bilateral nephrocalcinosis and amelogenesis imperfecta: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456756/
https://www.ncbi.nlm.nih.gov/pubmed/26097369
http://dx.doi.org/10.4103/0976-237X.156063
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