Familial Hypodontia: A Case Series

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Familial Hypodontia: A Case Series.

The phenomenon of congenitally missing teeth has been described with different names: hypodontia, oligodontia, anodontia, congenitally missing teeth and dental agenesis. The present paper reports familial hypodontia, involving two siblings from a single family. Case I reported the absence of 18, 12, 22 and 31 teeth whereas case II reported the absence of 31 and 41. On the evaluation of the two ...

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Phenotypic and Genotypic Features of Familial Hypodontia

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Introduction: Cleidocranial dysplasia is a rare hereditary autosomal dominant disorder which presents as a defect of the skeleton and the teeth. Case Report: The present case is of a 37 year old male patient with a complaint of difficulty in chewing due to multiple missing teeth. On examination, the pathognomonic triad of Cleidocranial Dysplasia, viz., multiple impacted supernumerary teeth, par...

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Purpose: The natural history and inheritance of familial papillary thyroid carcinoma (FPTC) remains unclear. A specific genetic defect responsible for this condition and its inheritance is yet to be established. The penetrance, mode of inheritance and treatment of this familial thyroid condition is different from other familial thyroid condition (familial medullary thyroid cancer). Presented he...

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ژورنال

عنوان ژورنال: Kathmandu University Medical Journal

سال: 2017

ISSN: 1812-2078,1812-2027

DOI: 10.3126/kumj.v13i2.16792