نتایج جستجو برای: primary congenital glaucoma

تعداد نتایج: 774492  

2013
Ta C. Chang Kara M. Cavuoto

Primary congenital glaucoma is a worldwide diagnostic and therapeutic challenge. Although medical management is often a temporizing measure, early surgical intervention is the definitive treatment. As the abundance of surgical treatment options continues to expand, the authors will compare and contrast the available options and attempt to provide a consensus on surgical management.

Journal: :Clinics 2006
Maria Aparecida Onuki Haddad Frederico José Correa Lobato Marcos Wilson Sampaio Newton Kara-José

OBJECTIVE To analyze data on the pediatric population attending the Ophthalmologic Clinic's Low Vision Service at the São Paulo University Medical School. METHODS Low vision ophthalmologic assessment, from April 1998 to December 2003, of 385 children and adolescents with mean age of 7 years; 51.7% males and 48.3% females. The main data analyzed were age, diagnosis, anatomic site of the ocular...

2004
D F Sena S Finzi K Rodgers E Del Bono J L Haines J L Wiggs

P rimary congenital glaucoma is an important cause of childhood blindness worldwide. In congenital glaucoma, the anterior segment of the eye fails to develop completely; this results, in particular, in malformation of the trabecular meshwork and aqueous outflow pathways. 2 Although sporadic cases arise frequently, many cases of congenital glaucoma are inherited as an autosomal recessive trait, ...

Journal: :Molecular vision 2005
Subhabrata Chakrabarti Kiranpreet Kaur Sreelatha Komatireddy Moulinath Acharya Koilkonda R Devi Arijit Mukhopadhyay Anil K Mandal Seyed E Hasnain Garudadri Chandrasekhar Ravi Thomas Kunal Ray

PURPOSE Myocilin gene defects have been originally implicated in primary open angle glaucoma (POAG). Based on multiple reports for the occurrence of Gln48His mutation (c.144G>T; HGMD accession number CM023962) among Indian POAG patients, we wanted to estimate the prevalence of this mutation in primary open angle and primary congenital glaucoma (PCG) in India and assess its role in the causation...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Na Luo Michael D Conwell Xingjuan Chen Christine Insinna Kettenhofen Christopher J Westlake Louis B Cantor Clark D Wells Robert N Weinreb Timothy W Corson Dan F Spandau Karen M Joos Carlo Iomini Alexander G Obukhov Yang Sun

Lowe syndrome is a rare X-linked congenital disease that presents with congenital cataracts and glaucoma, as well as renal and cerebral dysfunction. OCRL, an inositol polyphosphate 5-phosphatase, is mutated in Lowe syndrome. We previously showed that OCRL is involved in vesicular trafficking to the primary cilium. Primary cilia are sensory organelles on the surface of eukaryotic cells that medi...

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