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Hyper IgE Disorder Associated with Multiple Fused Primary Teeth: A Rare Clinical Occurrence

The hyperimmunoglobulin E syndrome (HIES) is a multisystem disorder that affects the dentition, skeleton, connective tissues and immune system. Little is known about oral manifestations of the syndrome. The purpose of this report was to describe a 6-year-old boy with suspected autosomal recessive HI...

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Autores principales: Sankar, AJ Sai, Kumar, MG Manoj, Samata, Y, Reddy, K Srikanth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993831/
https://www.ncbi.nlm.nih.gov/pubmed/27616847
http://dx.doi.org/10.5005/jp-journals-10005-1081i
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author Sankar, AJ Sai
Kumar, MG Manoj
Samata, Y
Reddy, K Srikanth
author_facet Sankar, AJ Sai
Kumar, MG Manoj
Samata, Y
Reddy, K Srikanth
author_sort Sankar, AJ Sai
collection PubMed
description The hyperimmunoglobulin E syndrome (HIES) is a multisystem disorder that affects the dentition, skeleton, connective tissues and immune system. Little is known about oral manifestations of the syndrome. The purpose of this report was to describe a 6-year-old boy with suspected autosomal recessive HIES syndrome who had multiple fused primary teeth, which is a rare association with JOB syndrome. The patient gave a history of pneumonia and skin infections. Recognition of such case at an early age is necessary to reduce morbidity. As conclusion, treatment for this condition is life long administration of therapeutic doses of penicillinase-resistant penicillin, with the addition of other antibiotics or antifungal agents as required for specific infections.
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spelling pubmed-49938312016-09-09 Hyper IgE Disorder Associated with Multiple Fused Primary Teeth: A Rare Clinical Occurrence Sankar, AJ Sai Kumar, MG Manoj Samata, Y Reddy, K Srikanth Int J Clin Pediatr Dent Case Report The hyperimmunoglobulin E syndrome (HIES) is a multisystem disorder that affects the dentition, skeleton, connective tissues and immune system. Little is known about oral manifestations of the syndrome. The purpose of this report was to describe a 6-year-old boy with suspected autosomal recessive HIES syndrome who had multiple fused primary teeth, which is a rare association with JOB syndrome. The patient gave a history of pneumonia and skin infections. Recognition of such case at an early age is necessary to reduce morbidity. As conclusion, treatment for this condition is life long administration of therapeutic doses of penicillinase-resistant penicillin, with the addition of other antibiotics or antifungal agents as required for specific infections. Jaypee Brothers Medical Publishers 2010 2010-09-15 /pmc/articles/PMC4993831/ /pubmed/27616847 http://dx.doi.org/10.5005/jp-journals-10005-1081i Text en Copyright © 2010; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Case Report
Sankar, AJ Sai
Kumar, MG Manoj
Samata, Y
Reddy, K Srikanth
Hyper IgE Disorder Associated with Multiple Fused Primary Teeth: A Rare Clinical Occurrence
title Hyper IgE Disorder Associated with Multiple Fused Primary Teeth: A Rare Clinical Occurrence
title_full Hyper IgE Disorder Associated with Multiple Fused Primary Teeth: A Rare Clinical Occurrence
title_fullStr Hyper IgE Disorder Associated with Multiple Fused Primary Teeth: A Rare Clinical Occurrence
title_full_unstemmed Hyper IgE Disorder Associated with Multiple Fused Primary Teeth: A Rare Clinical Occurrence
title_short Hyper IgE Disorder Associated with Multiple Fused Primary Teeth: A Rare Clinical Occurrence
title_sort hyper ige disorder associated with multiple fused primary teeth: a rare clinical occurrence
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993831/
https://www.ncbi.nlm.nih.gov/pubmed/27616847
http://dx.doi.org/10.5005/jp-journals-10005-1081i
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