Cargando…
Distal renal tubular acidosis and amelogenesis imperfecta: A rare association
Renal tubular acidosis (RTA) is characterized by a normal anion gap with hyperchloremic metabolic acidosis. Primary distal RTA (type I) is the most common RTA in children. Childhood presentation of distal RTA includes vomiting, failure to thrive, metabolic acidosis, and hypokalemia. Amelogenesis imp...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841516/ https://www.ncbi.nlm.nih.gov/pubmed/24339526 http://dx.doi.org/10.4103/0971-4065.120345 |
_version_ | 1782292789613035520 |
---|---|
author | Ravi, P. Ekambaranath, T. S. Arasi, S. Ellil Fernando, E. |
author_facet | Ravi, P. Ekambaranath, T. S. Arasi, S. Ellil Fernando, E. |
author_sort | Ravi, P. |
collection | PubMed |
description | Renal tubular acidosis (RTA) is characterized by a normal anion gap with hyperchloremic metabolic acidosis. Primary distal RTA (type I) is the most common RTA in children. Childhood presentation of distal RTA includes vomiting, failure to thrive, metabolic acidosis, and hypokalemia. Amelogenesis imperfecta (AI) represents a condition where the dental enamel and oral tissues are affected in an equal manner resulting in the hypoplastic or hypopigmented teeth. We report a 10-year-old girl, previously asymptomatic presented with the hypokalemic paralysis and on work-up found out to have type I RTA. The discoloration of teeth and enamel was diagnosed as AI. |
format | Online Article Text |
id | pubmed-3841516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38415162013-12-11 Distal renal tubular acidosis and amelogenesis imperfecta: A rare association Ravi, P. Ekambaranath, T. S. Arasi, S. Ellil Fernando, E. Indian J Nephrol Case Report Renal tubular acidosis (RTA) is characterized by a normal anion gap with hyperchloremic metabolic acidosis. Primary distal RTA (type I) is the most common RTA in children. Childhood presentation of distal RTA includes vomiting, failure to thrive, metabolic acidosis, and hypokalemia. Amelogenesis imperfecta (AI) represents a condition where the dental enamel and oral tissues are affected in an equal manner resulting in the hypoplastic or hypopigmented teeth. We report a 10-year-old girl, previously asymptomatic presented with the hypokalemic paralysis and on work-up found out to have type I RTA. The discoloration of teeth and enamel was diagnosed as AI. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3841516/ /pubmed/24339526 http://dx.doi.org/10.4103/0971-4065.120345 Text en Copyright: © Indian Journal of Nephrology 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 Ravi, P. Ekambaranath, T. S. Arasi, S. Ellil Fernando, E. Distal renal tubular acidosis and amelogenesis imperfecta: A rare association |
title | Distal renal tubular acidosis and amelogenesis imperfecta: A rare association |
title_full | Distal renal tubular acidosis and amelogenesis imperfecta: A rare association |
title_fullStr | Distal renal tubular acidosis and amelogenesis imperfecta: A rare association |
title_full_unstemmed | Distal renal tubular acidosis and amelogenesis imperfecta: A rare association |
title_short | Distal renal tubular acidosis and amelogenesis imperfecta: A rare association |
title_sort | distal renal tubular acidosis and amelogenesis imperfecta: a rare association |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841516/ https://www.ncbi.nlm.nih.gov/pubmed/24339526 http://dx.doi.org/10.4103/0971-4065.120345 |
work_keys_str_mv | AT ravip distalrenaltubularacidosisandamelogenesisimperfectaarareassociation AT ekambaranathts distalrenaltubularacidosisandamelogenesisimperfectaarareassociation AT arasisellil distalrenaltubularacidosisandamelogenesisimperfectaarareassociation AT fernandoe distalrenaltubularacidosisandamelogenesisimperfectaarareassociation |