The Unyielding Enigma
Scleroderma, an autoimmune connective tissue disorder marked by profound fibrosis in visceral organs, skin, and blood vessels, exhibits oral manifestations typically initiating with tongue rigidity and facial skin alterations. It presents with a plethora of radiological and systemic presentations. T...
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Format: | Article |
Language: | English |
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Wolters Kluwer Medknow Publications
2024-12-01
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Series: | Journal of Indian Academy of Oral Medicine and Radiology |
Subjects: | |
Online Access: | https://journals.lww.com/10.4103/jiaomr.jiaomr_80_24 |
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author | Hima John Jiss Mary Jeslin James S Devu |
author_facet | Hima John Jiss Mary Jeslin James S Devu |
author_sort | Hima John |
collection | DOAJ |
description | Scleroderma, an autoimmune connective tissue disorder marked by profound fibrosis in visceral organs, skin, and blood vessels, exhibits oral manifestations typically initiating with tongue rigidity and facial skin alterations. It presents with a plethora of radiological and systemic presentations. This case report details the clinical and radiographic features of a 45-year-old female and a 30-year-old male, both presenting classic manifestations of the disease and a short review of literature has been made. |
format | Article |
id | doaj-art-a086cd00962f434c86ca22ad47498914 |
institution | Kabale University |
issn | 0972-1363 0975-1572 |
language | English |
publishDate | 2024-12-01 |
publisher | Wolters Kluwer Medknow Publications |
record_format | Article |
series | Journal of Indian Academy of Oral Medicine and Radiology |
spelling | doaj-art-a086cd00962f434c86ca22ad474989142025-01-06T15:40:05ZengWolters Kluwer Medknow PublicationsJournal of Indian Academy of Oral Medicine and Radiology0972-13630975-15722024-12-0136446346410.4103/jiaomr.jiaomr_80_24The Unyielding EnigmaHima JohnJiss MaryJeslin JamesS DevuScleroderma, an autoimmune connective tissue disorder marked by profound fibrosis in visceral organs, skin, and blood vessels, exhibits oral manifestations typically initiating with tongue rigidity and facial skin alterations. It presents with a plethora of radiological and systemic presentations. This case report details the clinical and radiographic features of a 45-year-old female and a 30-year-old male, both presenting classic manifestations of the disease and a short review of literature has been made.https://journals.lww.com/10.4103/jiaomr.jiaomr_80_24autoimmunecalcinosis cutissclerodactylysclerosis |
spellingShingle | Hima John Jiss Mary Jeslin James S Devu The Unyielding Enigma Journal of Indian Academy of Oral Medicine and Radiology autoimmune calcinosis cutis sclerodactyly sclerosis |
title | The Unyielding Enigma |
title_full | The Unyielding Enigma |
title_fullStr | The Unyielding Enigma |
title_full_unstemmed | The Unyielding Enigma |
title_short | The Unyielding Enigma |
title_sort | unyielding enigma |
topic | autoimmune calcinosis cutis sclerodactyly sclerosis |
url | https://journals.lww.com/10.4103/jiaomr.jiaomr_80_24 |
work_keys_str_mv | AT himajohn theunyieldingenigma AT jissmary theunyieldingenigma AT jeslinjames theunyieldingenigma AT sdevu theunyieldingenigma AT himajohn unyieldingenigma AT jissmary unyieldingenigma AT jeslinjames unyieldingenigma AT sdevu unyieldingenigma |