Congenital absence of lingual frenum in a non-syndromic patient: a case report
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چکیده
منابع مشابه
Bilateral Dentigerous Cysts in a Non-Syndromic Patient: Literature Review and Report of a Case
Introduction: Dentigerous cysts (DCs) are the most common developmental cysts of the jaws, mostly associated with impacted third molars and canines. Multiple or bilateral DCs are rare and typically occur in association with some syndromes including cleidocranial dysplasia and Gorlin-Goltz. The occurrence of multiple DCs is rare in the absence of these syndromes. Case Presentation: A 28-year-ol...
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Non-syndromic bilateral humeroradial synostosis is a very rare congenital anomalies of the upper limbs. This condition often occurs in conjunction with various syndromes and is associated with a positive family history. Herein, we report a 6 year old boy with non-syndromic bilateral humeroradial synostosis, without aplasia, hypoplasia or family history. Both elbows were constant at 90 degrees f...
متن کاملsequential supernumerary teeth development in a non-syndromic patient; report of a rare case.
isolated impacted supernumerary teeth are quite rare, but they can be seen associated with several syndromes such as cleidocranial dysostosis or gardner's syndrome. this article aims to discuss a case of sequential formation of supernumerary teeth with no other associated disease or syndrome. a 17-year-old iranian male with 8 impacted supernumerary teeth was referred to the department of pediat...
متن کاملCongenital Hemangiopericytoma: A Case Report
Hemangiopericytoma is a rare vascular tumor observed mostly in adults. It usually presents with a painless slowly enlarging mass. The infantile type with much rarer occurrence has a different course compared to adults. Very few case reports have been described in the literature with disease onset in the infancy. The first reported case of infantile hemangiopericytoma of limbs from the Middle ...
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ژورنال
عنوان ژورنال: Journal of Medical Case Reports
سال: 2019
ISSN: 1752-1947
DOI: 10.1186/s13256-018-1966-7