Literature DB >> 14998213

Lenz microphthalmia syndrome with dental anomalies: a case report.

Nazan Kocatas Ersin1, Zuhal Tugsel, Bülent Gökce, Birgül Ozpinar, Nesrin Eronat.   

Abstract

This report describes the dental management and 7-year follow-up of a 14-year-old boy who showed the typical characteristics of Lenz microphthalmia syndrome, a rare genetic disorder characterized by multiple abnormalities. The main features of the syndrome are microphthalmia, developmental retardation, ear abnormalities, microcephaly, skeletal, digital and urogenital anomalies. The dental anomalies include micrognathia, hypodontia, agenesis of permanent teeth, conic-shaped incisors, and taurodontic molars. The purpose of the report was to document specific oral manifestations and dental anomalies and their management associated with a previously reported case.

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Mesh:

Year:  2003        PMID: 14998213

Source DB:  PubMed          Journal:  J Dent Child (Chic)        ISSN: 1551-8949


  3 in total

1.  BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects.

Authors:  Emma Hilton; Jennifer Johnston; Sandra Whalen; Nobuhiko Okamoto; Yoshikazu Hatsukawa; Juntaro Nishio; Hiroshi Kohara; Yoshiko Hirano; Seiji Mizuno; Chiharu Torii; Kenjiro Kosaki; Sylvie Manouvrier; Odile Boute; Rahat Perveen; Caroline Law; Anthony Moore; David Fitzpatrick; Johannes Lemke; Florence Fellmann; François-Guillaume Debray; Florence Dastot-Le-Moal; Marion Gerard; Josiane Martin; Pierre Bitoun; Michel Goossens; Alain Verloes; Albert Schinzel; Deborah Bartholdi; Tanya Bardakjian; Beverly Hay; Kim Jenny; Kathreen Johnston; Michael Lyons; John W Belmont; Leslie G Biesecker; Irina Giurgea; Graeme Black
Journal:  Eur J Hum Genet       Date:  2009-04-15       Impact factor: 4.246

2.  Endodontic management of a hypertaurodontic tooth associated with 48, XXYY syndrome: A review and case report.

Authors:  Sridevi Krishnamoorthy; Velayutham Gopikrishna
Journal:  J Conserv Dent       Date:  2015 May-Jun

3.  Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing.

Authors:  Jianlong Zhuang; Chunnuan Chen; Yu'e Chen; Shuhong Zeng; Yuying Jiang; Yuanbai Wang; Xinying Chen; Yingjun Xie; Gaoxiong Wang
Journal:  Front Genet       Date:  2022-03-25       Impact factor: 4.599

  3 in total

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