نتایج جستجو برای: oligodontia

تعداد نتایج: 244  

Journal: :journal of dentistry, tehran university of medical sciences 0
l chandrashekar reader, department of oral medicine and radiology, best dental science college and hospital madurai, tamilnadu, india. k r kashinath principal, professor and head, department of prosthodontics, sri siddhartha dental college and hospital, tumkur, india. setty suhas professor, department of oral medicine and radiology, sri siddhartha dental college and hospital, tumkur, india.

developmental disturbances of the tongue (aglossia, macroglossia, microglossia, and ankyloglossia) can adversely affect the development of the surrounding structures including the palate, alveolar process, and teeth. these developmental disturbances impair functions such as mastication, speech, and swallowing. ankyloglossia is of various types and may be associated with other syndromic features...

2016
Hyeon-Goo Kang Yoon-Hyuk Huh Chan-Jin Park Lee-Ra Cho

Oligodontia is defined as a congenital tooth agenesis with the absence of six or more permanent teeth. This clinical report describes a patient with non-syndromic partial oligodontia, with retained deciduous teeth and the absence of 16 permanent teeth. Anterior esthetic problems were caused by interarch tooth size discrepancy, interdental space, aberrant tooth dimensions, and the absence of cen...

2013
Huiying He Dong Han Hailan Feng Hong Qu Shujuan Song Baojing Bai Zhenting Zhang

BACKGROUND Dental agenesis is the most common, often heritable, developmental anomaly in humans. Although WNT10A gene mutations are known to cause rare syndromes associated with tooth agenesis, including onycho-odontodermal dysplasia (OODD), Schöpf-Schulz-Passarge syndrome (SSPS), hypohidrotic ectodermal dysplasia (HED), and more than half of the cases of isolated oligodontia recently, the geno...

Journal: :American journal of human genetics 2004
Laura Lammi Sirpa Arte Mirja Somer Heikki Jarvinen Paivi Lahermo Irma Thesleff Sinikka Pirinen Pekka Nieminen

Wnt signaling regulates embryonic pattern formation and morphogenesis of most organs. Aberrations of regulation of Wnt signaling may lead to cancer. Here, we have used positional cloning to identify the causative mutation in a Finnish family in which severe permanent tooth agenesis (oligodontia) and colorectal neoplasia segregate with dominant inheritance. Eleven members of the family lacked at...

Journal: :Journal of Indian Academy of Oral Medicine and Radiology 2015

Journal: :Medical Journal Armed Forces India 2008

Journal: :West African journal of medicine 2010
O O Bankole O I Iyun O O Dosunmu

BACKGROUND oligodontia is a condition with developmental absence of six or more permanent teeth excluding the third molars. It is a rare finding which has not been frequently documented in Nigerian children. OBJECTIVE to report a case of non syndromic oligodontia. METHODS The details of the clinical presentation, course and outcome of a 9-year-old child with oligodontia were reviewed. The c...

2016
Afnan I Al-Saleem Asma M Al-Jobair

Congenital malformations might occur because of environmental or genetic factors, and sometimes occur because of unknown causes. Acetazolamide is a carbonic anhydrase inhibitor that is used to treat idiopathic intracranial hypertension, glaucoma, and epilepsy. The use of acetazolamide has not been recommended for pregnant women because of reported teratogenic risks. Congenital malformations, su...

2017
Jyothirmai Talasila Ramaswamy Pachigolla Kiranmai V S N Yarlagadda Ramu Vuppala Karl-Heinz Grzeschik Sai Kiran K V S Catherine M Rose Gary S Gottesman Zsolt Urban

This case report describes a patient with ankyloglossia, oligodontia, unilateral hypoplasia of the zygoma and mandible, along with bilateral distal reduction anomalies of his limbs without long bone abnormalities. This may represent a mild variant of oromandibular limb hypogenesis syndrome, expanding the phenotypic spectrum, or a previously unrecognized malformation syndrome.

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