Results 41 to 50 of about 5,069,987 (201)

Comparison between results of trabeculectomy in primary congenital glaucoma with and without the use of mitomycin C

, 2004
Purpose: To evaluate the results of trabeculectomy with and without the use of mitomycin C in children with primary congenital glaucoma.Methods: the authors retrospectively studied the data of 91 patients who underwent the first trabeculectomy for ...
Montesano, Fabio Tadeu [UNIFESP], Rodrigues, Adriana Maria [UNIFESP], Prata Junior, João Antonio [UNIFESP], Mello, Paulo Augusto de Arruda [UNIFESP], Paranhos Junior, Augusto [UNIFESP]   +4 more
core   +1 more source

Rare case of primary congenital glaucoma with hypoplasia corpus callosum [PDF]

, 2018
Primary congenital glaucoma is a rare disease that causes elevated intraocular pressure within the first three years of life. Few studies have explored the association of primary congenital glaucoma with malformation of corpus callosum.
Risa Etika, -, Agus Harianto, -, Darto Saharso, -, Prastiya Indra Gunawan, -, Nurwasis, -, Evelyn Komaratih, -   +5 more
core   +2 more sources

CYP1B1 Gene Analysis in Primary Congenital Glaucoma Brazilian Patients Novel Mutations and Association With Poor Prognosis

, 2010
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Purpose: To determine the spectrum of CYP1B1 gene mutations in Brazilian patients with primary congenital glaucoma, and to correlate the presence of alterations in the CYP1B1 gene sequence with
Umbelino, CC, Richeti, F, Costa, VP, de Vasconcellos, JPC, de Melo, MB, Kasahara, N, Della Paolera, M, Rocha, MN, Tavares, A, Vital Paulino Costa, José Paulo Cabral de Vasconcellos, Flávio Richeti, Mylene Neves Rocha, Niro Kasahara, Anderson Tavares, Maurício Della Paolera, Mônica Barbosa de Melo, Cristiano Caixeta Umbelino   +17 more
core   +1 more source

Prevalence of pre-iridal monocellular and fibrovascular membranes in canine globes affected with congenital glaucoma associated with anterior segment dysgenesis, primary glaucoma associated with goniodysgenesis, and secondary glaucoma

Frontiers in Veterinary Science
ObjectivesThe objectives of this study were to (i) evaluate the prevalence of pre-iridal monocellular and fibrovascular membranes in canine globes affected with congenital glaucoma associated with anterior segment dysgenesis (ASD), primary glaucoma ...
Leila Bedos, Lynne Sandmeyer, John Campbell, Bruce H. Grahn   +3 more
doaj   +1 more source

Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT LRP1 encodes the low‐density lipoprotein (LDL) receptor‐related protein 1 (LRP1), a transmembrane protein involved in endocytosis and activation of multiple signaling pathways. LRP1 variants have been implicated in the pathogenesis of congenital heart defects (CHD), Alzheimer's disease, and neurodevelopmental disorders (NDD).
Alyssa L. Rippert, Gudny Anna Arnadottir, Laura Bedinger, Nicola Brunetti‐Pierri, Jennifer Cech, Xin Chen, Yanmin Chen, Erika Chick, Sarah Dyack, Madeleine Franchi, Tanja Frey, David Genevieve, Ian Glass, Jorge Granadillo, Kelly A. Keener, Sara B. MacKay, Paige McDunnah, Vinod K. Misra, Kristin G. Monaghan, Sureni V. Mullegama, Cristina Peduto, Leia Peterman‐Prather, Anita Rauch, Cherith Somerville, Kari Stefansson, Katharina Steindl, Patrick Sulem, Telma Sulem, Pamela Trapane, Roberta Zeuli, Samuel Zinner, Kosuke Izumi   +31 more
wiley   +1 more source

Pattern of Childhood Glaucoma

Journal of Nepal Medical Association, 2013
Glaucoma is one of the important causes of blindness in children all over the world1 . Childhood glaucoma encompasses a wide variety of conditions ranging from primary congenital glaucoma to different acquired varieties.
S Shakya, S Koirala, E Pradhan
doaj   +1 more source

Biallelic PAX6 Variants in an Adult With Severe Microphthalmia and Preserved Intellectual Function

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT PAX6 encodes a dosage‐sensitive transcription factor that is essential for eye development. Heterozygous PAX6 disease is well characterized, but biallelic disease is extremely rare and has been associated with anophthalmia, severe brain malformations, and perinatal lethality.
Karl De Geer, Britt‐Marie Anderlid, Lena Jacobson, Daniel Martín Muñoz, Erik Björck   +4 more
wiley   +1 more source

Spontaneous resolution of primary congenital glaucoma [PDF]

Australian and New Zealand Journal of Ophthalmology, 1989
AbstractWe report a further four cases of spontaneously resolved primary congenital glaucoma, including one case seen bath prior and subsequent to the resolution. This condition is detected usually in eyes with megalocornea, which are later found to have breaks in Descemets membrane.
P, Lockie, J, Elder
openaire   +2 more sources

An investigation of genetic risk factors in primary open-angle glaucoma [PDF]

, 2009
Primary open-angle glaucoma (POAG) is a multifactorial disease with a strong genetic component. Notably however, few genes have been robustly associated with POAG in the general population.
Park, S.
core  

Primary Congenital Glaucoma in Kano, Northern Nigeria

, 2008
Primary congenital glaucoma is one of the causes of childhood blindness and it appears to be common in our environment. This study evaluated the pattern of presentation and management of primary congenital glaucoma in children.
Lawan, A
core   +1 more source