دورية أكاديمية
Achondroplasia with Polydactyly: A Case Report
| العنوان: | Achondroplasia with Polydactyly: A Case Report |
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| المؤلفون: | Caroline Frank, Sameeya Sharif, Muddepalle Pavani, Balasubramanian Karthika, Sridhar Thathekalva |
| المصدر: | Journal of Clinical and Diagnostic Research, Vol 11, Iss 3, Pp ZD14-ZD15 (2017) |
| بيانات النشر: | JCDR Research and Publications Private Limited, 2017. |
| سنة النشر: | 2017 |
| المجموعة: | LCC:Medicine |
| مصطلحات موضوعية: | delayed eruption, dental caries, short stature, Medicine |
| الوصف: | An eight-year-old girl child reported to the Department of Oral Medicine and Radiology with the chief complaint of unerupted permanent teeth for past two years. The child presented features like disproportionately short stature, rhizomelic shortening of arms and legs, long face, frontal bossing and saddle nose. Based on the findings of chest and spine radiographs and ultrasound the case was diagnosed as a rare bone disorder “Achondroplasia”. This case also presents a unique feature of polydactyly. Polydactyly is a manifestation in clinical medicine because it can serve as an indicator for a plethora of congenital anamolies. This case gained dental interest because of its characteristic craniofacial features. This article highlights the peculiar manifestations of this anamoly. |
| نوع الوثيقة: | article |
| وصف الملف: | electronic resource |
| اللغة: | English |
| تدمد: | 2249-782X 0973-709X |
| Relation: | https://jcdr.net/articles/PDF/9477/24678_CE[Ra1]_F(GH)_PF1(PrG_RK)_PFA(GH)_PF2(NE_SY_DK).pdf; https://doaj.org/toc/2249-782X; https://doaj.org/toc/0973-709X |
| DOI: | 10.7860/JCDR/2017/24678.9477 |
| URL الوصول: | https://doaj.org/article/a6884e99af5d44559eaa1a1d3a37b49e |
| رقم الأكسشن: | edsdoj.6884e99af5d44559eaa1a1d3a37b49e |
| قاعدة البيانات: | Directory of Open Access Journals |
Full Text Finder | تدمد: | 2249782X 0973709X |
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| DOI: | 10.7860/JCDR/2017/24678.9477 |