Literature DB >> 3276203

The Lenz microphthalmia syndrome.

E I Traboulsi1, W Lenz, M Gonzales-Ramos, J Siegel, W G Macrae, I H Maumenee.   

Abstract

We examined two patients with the Lenz microphthalmia syndrome. When findings from these two patients and those from ten other patients in the literature were combined, the following abnormalities were observed: microphthalmos in all patients; developmental retardation in 11 patients (92%); external ear abnormalities in ten patients (83%); microcephaly in ten patients (83%); blepharoptosis in nine patients (75%); skeletal anomalies (excluding digital anomalies) in eight patients (67%); dental abnormalities of number and position in eight patients (67%); digital anomalies in seven patients (58%); urogenital anomalies in six patients (50%); and cleft lip and palate abnormalities in four patients (33%). Cardiac anomalies, imperforate anus, hearing loss, spastic diplegia, sacral pits, webbed neck, and abnormal dermatoglyphs were rarely seen. One of our two patients had a dislocated lens and retinal detachment.

Entities:  

Mesh:

Year:  1988        PMID: 3276203     DOI: 10.1016/0002-9394(88)90119-5

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  11 in total

1.  A case of Lenz microphthalmia syndrome.

Authors:  F F Ozkinay; C Ozkinay; H Yüksel; A Yenigun; G Sapmaz; O Aksu
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

2.  Colobomatous malformations of the eye.

Authors:  I H Maumenee; T N Mitchell
Journal:  Trans Am Ophthalmol Soc       Date:  1990

Review 3.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

4.  Lenz microphthalmia syndrome?

Authors:  Ramachandran Sudarshan; Rajeshwari G Annigeri
Journal:  Wien Klin Wochenschr       Date:  2011-02       Impact factor: 1.704

5.  A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndrome.

Authors:  Taraneh Esmailpour; Hamidreza Riazifar; Linan Liu; Sandra Donkervoort; Vincent H Huang; Shreshtha Madaan; Bassem M Shoucri; Anke Busch; Jie Wu; Alexander Towbin; Robert B Chadwick; Adolfo Sequeira; Marquis P Vawter; Guoli Sun; Jennifer J Johnston; Leslie G Biesecker; Riki Kawaguchi; Hui Sun; Virginia Kimonis; Taosheng Huang
Journal:  J Med Genet       Date:  2014-01-15       Impact factor: 6.318

6.  Megarbane syndrome.

Authors:  Caglayan Ahmet Okay; Dundar Munis
Journal:  Indian J Hum Genet       Date:  2008-01

7.  Anophthalmia with cleft palate and micrognathia: a new syndrome?

Authors:  S R Phadke; A K Sharma; S S Agarwal
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

8.  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

9.  Lenz microphthalmic syndrome in an Indian patient.

Authors:  Arvind Gupta; Renuka Srinivasan; Datta G Pandian; K Ramesh Babu
Journal:  Indian J Ophthalmol       Date:  2007 Nov-Dec       Impact factor: 1.848

Review 10.  NAA10-related syndrome.

Authors:  Yiyang Wu; Gholson J Lyon
Journal:  Exp Mol Med       Date:  2018-07-27       Impact factor: 8.718

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