Mucopolysaccharidoses type IV A (Morquio syndrome): A case series of three siblings
Mucopolysaccharidoses (MPS) are a family of inherited metabolic diseases that results from the deficiency of lysosomal enzymes involved in the degradation of the glycosaminoglycans (mucopolysaccharides). Despite the well-documented oral and dental findings of MPS type IV, there is not much literatur...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2012-01-01
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| Series: | Journal of Indian Society of Pedodontics and Preventive Dentistry |
| Subjects: | |
| Online Access: | http://www.jisppd.com/article.asp?issn=0970-4388;year=2012;volume=30;issue=1;spage=66;epage=69;aulast=Rekka |
| _version_ | 1818543009321451520 |
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| author | P Rekka P V Rathna S Jagadeesh S Seshadri |
| author_facet | P Rekka P V Rathna S Jagadeesh S Seshadri |
| author_sort | P Rekka |
| collection | DOAJ |
| description | Mucopolysaccharidoses (MPS) are a family of inherited metabolic diseases that results from the deficiency of lysosomal enzymes involved in the degradation of the glycosaminoglycans (mucopolysaccharides). Despite the well-documented oral and dental findings of MPS type IV, there is not much literature documented about the incidence of this disorder among siblings in the same family. This report outlines the clinical and radiographic findings found in three siblings with Morquio syndrome. |
| first_indexed | 2024-12-11T22:29:39Z |
| format | Article |
| id | doaj.art-bfaf40adab574a688f934df3cabdbd74 |
| institution | Directory Open Access Journal |
| issn | 0970-4388 1998-3905 |
| language | English |
| last_indexed | 2024-12-11T22:29:39Z |
| publishDate | 2012-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Journal of Indian Society of Pedodontics and Preventive Dentistry |
| spelling | doaj.art-bfaf40adab574a688f934df3cabdbd742022-12-22T00:48:11ZengWolters Kluwer Medknow PublicationsJournal of Indian Society of Pedodontics and Preventive Dentistry0970-43881998-39052012-01-01301666910.4103/0970-4388.95586Mucopolysaccharidoses type IV A (Morquio syndrome): A case series of three siblingsP RekkaP V RathnaS JagadeeshS SeshadriMucopolysaccharidoses (MPS) are a family of inherited metabolic diseases that results from the deficiency of lysosomal enzymes involved in the degradation of the glycosaminoglycans (mucopolysaccharides). Despite the well-documented oral and dental findings of MPS type IV, there is not much literature documented about the incidence of this disorder among siblings in the same family. This report outlines the clinical and radiographic findings found in three siblings with Morquio syndrome.http://www.jisppd.com/article.asp?issn=0970-4388;year=2012;volume=30;issue=1;spage=66;epage=69;aulast=RekkaMorquio syndromemucopolysaccharidoses type IVAMucopolysaccharidoses |
| spellingShingle | P Rekka P V Rathna S Jagadeesh S Seshadri Mucopolysaccharidoses type IV A (Morquio syndrome): A case series of three siblings Journal of Indian Society of Pedodontics and Preventive Dentistry Morquio syndrome mucopolysaccharidoses type IVA Mucopolysaccharidoses |
| title | Mucopolysaccharidoses type IV A (Morquio syndrome): A case series of three siblings |
| title_full | Mucopolysaccharidoses type IV A (Morquio syndrome): A case series of three siblings |
| title_fullStr | Mucopolysaccharidoses type IV A (Morquio syndrome): A case series of three siblings |
| title_full_unstemmed | Mucopolysaccharidoses type IV A (Morquio syndrome): A case series of three siblings |
| title_short | Mucopolysaccharidoses type IV A (Morquio syndrome): A case series of three siblings |
| title_sort | mucopolysaccharidoses type iv a morquio syndrome a case series of three siblings |
| topic | Morquio syndrome mucopolysaccharidoses type IVA Mucopolysaccharidoses |
| url | http://www.jisppd.com/article.asp?issn=0970-4388;year=2012;volume=30;issue=1;spage=66;epage=69;aulast=Rekka |
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