نتایج جستجو برای: microphthalmia

تعداد نتایج: 1639  

Journal: :The American Journal of Pathology 1999

Journal: :Clinical genetics 2014
L Roos M Fang C Dali H Jensen N Christoffersen B Wu J Zhang R Xu P Harris X Xu K Grønskov Z Tümer

Anomalies of eye development can lead to the rare eye malformations microphthalmia and anophthalmia (small or absent ocular globes), which are genetically very heterogeneous. Several genes have been associated with microphthalmia and anophthalmia, and exome sequencing has contributed to the identification of new genes. Very recently, homozygous variations within ALDH1A3 have been associated wit...

Journal: :The British journal of ophthalmology 1999
D A Bessant K Anwar S Khaliq A Hameed M Ismail A M Payne S Q Mehdi S S Bhattacharya

BACKGROUND Congenital microphthalmia (OMIM: 309700) may occur in isolation or in association with a variety of systemic malformations. Isolated microphthalmia may be inherited as an autosomal dominant, an autosomal recessive, or an X linked trait. METHODS Based on a whole genome linkage analysis, in a six generation consanguineous family with autosomal recessive inheritance, the first locus f...

Journal: :American Journal of Obstetrics and Gynecology 2019

Journal: :British Journal of Ophthalmology 1926

2010
Doreen Becker Jens Tetens Adrian Brunner Daniela Bürstel Martin Ganter James Kijas Cord Drögemüller

Microphthalmia in sheep is an autosomal recessive inherited congenital anomaly found within the Texel breed. It is characterized by extremely small or absent eyes and affected lambs are absolutely blind. For the first time, we use a genome-wide ovine SNP array for positional cloning of a Mendelian trait in sheep. Genotyping 23 cases and 23 controls using Illumina's OvineSNP50 BeadChip allowed u...

2010
Ryan Chao Linda Nevin Pooja Agarwal Jan Riemer Xiaoyang Bai Allen Delaney Matthew Akana Nelson JimenezLopez Tanya Bardakjian Adele Schneider Nicolas Chassaing Daniel F. Schorderet David FitzPatrick Pui-yan Kwok Lars Ellgaard Douglas B. Gould Yan Zhang Jarema Malicki Herwig Baier Anne Slavotinek

Anophthalmia and microphthalmia are important birth defects, but their pathogenesis remains incompletely understood. We studied a patient with severe unilateral microphthalmia who had a 2.7 Mb deletion at chromosome 18q22.1 that was inherited from his mother. In-situ hybridization showed that one of the deleted genes, TMX3, was expressed in the retinal neuroepithelium and lens epithelium in the...

2014
Hiram Larangeira de Almeida Jr. Gabriela Rossi Luciana Boff de Abreu Cristina Bergamaschi Alessandra Banaszeski da Silva Kerstin Kutsche

The association of microphthalmia and linear skin defects was named microphthalmia with linear skin defects syndrome (MLS) or MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea), an X-chromosomal disorder manifesting mainly in females. We examined a female newborn with facial linear skin defects following the Blaschko lines. Computer tomography and ophthalmological examination con...

Journal: :genetics in the 3rd millennium 0
فائزه مجاهدی faezeh mojahedi

microphthalmia is defined as a globe with a total axial length that is at least two standard deviations below the mean for age. it may be isolated or part of a syndrome with other associated anomalies. causes can be divided into environmental, heritable or unknown. some researchers believe that microphthalmia and anophthalmia belong to one family. unilateral and bilateral anophtalmia have been ...

Journal: :Wiener klinische Wochenschrift 2011

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