Trismus‐pseudocamptodactyly syndrome with bilateral hypoplastic mandibular condyles and shallow mandibular fossa: A case report
| العنوان: | Trismus‐pseudocamptodactyly syndrome with bilateral hypoplastic mandibular condyles and shallow mandibular fossa: A case report |
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| المؤلفون: | Rika Kosaki, Kazumi Izawa, Tomonobu Hasegawa, Naoaki Hori, Gen Nishimura, Chieko Kusano |
| المصدر: | Oral Science International. 15:90-82 |
| بيانات النشر: | Wiley, 2018. |
| سنة النشر: | 2018 |
| مصطلحات موضوعية: | 0301 basic medicine, Orthodontics, Mandibular Condyles, business.industry, Bilateral hyperplasia, Trismus pseudocamptodactyly syndrome, 030105 genetics & heredity, Trismus, Distal arthrogryposis, Condyle, stomatognathic diseases, 03 medical and health sciences, Hecht syndrome, medicine.anatomical_structure, stomatognathic system, Otorhinolaryngology, Mandibular fossa, Medicine, medicine.symptom, business |
| الوصف: | Trismus-pseudocamptodactyly syndrome (TPS) (OMIM#158300), also known as Hecht syndrome, is a rare autosomal dominant distal arthrogryposis. Bilateral hyperplasia of the coronoid processes has been reported to cause trismus. In this study, we report a case of TPS definitively diagnosed on the basis of clinical signs in a patient who had bilateral hypoplastic mandibular condyles and shallow mandibular fossa; TPS in such patients have never been reported in the literature. On the basis of the present case, we propose that a hypoplastic mandibular condyle and shallow mandibular fossa are also clinical features of TPS. |
| تدمد: | 1881-4204 1348-8643 |
| URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_________::709cc0538fee89196f5e841e1923b5b1 https://doi.org/10.1016/s1348-8643(18)30008-9 |
| حقوق: | OPEN |
| رقم الأكسشن: | edsair.doi...........709cc0538fee89196f5e841e1923b5b1 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 18814204 13488643 |
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