Cargando…

Association of IGF1 polymorphisms with exotropia in a Pakistani cohort

PURPOSE: Strabismus (STBMS) is a multifactorial ocular disorder in children that leads to misalignment of the eyes. Insulin-like growth factor 1 (IGF1) has been shown to be involved in the development of extraocular muscles and myopia; however, data are limited on the genetic associations of IGF1 wi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zehra, Zainab, Khan, Netasha, Nadeem, Minhal, Siddiqui, Sorath Noorani, von Bartheld, Christopher S., Azam, Maleeha, Qamar, Raheel
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Molecular Vision 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9603902/ https://www.ncbi.nlm.nih.gov/pubmed/36338665

Ejemplares similares

The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families
por: Keser, Vafa, et al.
Publicado: (2017)

Exome Sequencing Identifies a Biallelic GALNS Variant (p.Asp233Asn) Causing Mucopolysaccharidosis Type IVA in a Pakistani Consanguineous Family
por: Ghafoor, Saima, et al.
Publicado: (2022)

A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family
por: Azam, Maleeha, et al.
Publicado: (2009)

Mutation screening of the CYP1B1 gene reveals thirteen novel disease-causing variants in consanguineous Pakistani families causing primary congenital glaucoma
por: Tehreem, Raeesa, et al.
Publicado: (2022)

Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families
por: Micheal, Shazia, et al.
Publicado: (2018)

Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome
por: Micheal, Shazia, et al.
Publicado: (2015)

Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts
por: Ayub, Humaira, et al.
Publicado: (2010)

Targeted gene sequencing of FYCO1 identified a novel mutation in a Pakistani family for autosomal recessive congenital cataract
por: Saleem, Rani Saira, et al.
Publicado: (2022)

Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma
por: Micheal, Shazia, et al.
Publicado: (2015)

Role of Lysyl oxidase-like 1 gene polymorphisms in Pakistani patients with pseudoexfoliative glaucoma
por: Micheal, Shazia, et al.
Publicado: (2012)

Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani families
por: Ajmal, Muhammad, et al.
Publicado: (2012)

Effects of Artisan aphakic intraocular lens on central corneal thickness and intra ocular pressure in pediatric eyes with crystalline subluxated lenses
por: Zafar, Saemah Nuzhat, et al.
Publicado: (2013)

The association of glutathione S-transferase GSTT1 and GSTM1 gene polymorphism with pseudoexfoliative glaucoma in a Pakistani population
por: Khan, Muhammad Imran, et al.
Publicado: (2010)

Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum
por: Maria, Maleeha, et al.
Publicado: (2016)

Variants in the PRPF8 Gene are Associated with Glaucoma
por: Micheal, Shazia, et al.
Publicado: (2017)

Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia
por: Azam, Maleeha, et al.
Publicado: (2010)

Association of tumor necrosis factor alpha gene polymorphism G-308A with pseudoexfoliative glaucoma in the Pakistani population
por: Khan, Muhammad Imran, et al.
Publicado: (2009)

Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families
por: Shafique, Sobia, et al.
Publicado: (2014)

Protective and pathogenic role of collagen subtypes genes COL4A3 and COL4A4 polymorphisms in the onset of keratoconus in South-Asian Pakistani cohort
por: Khashim Alswailmi, Farhan, et al.
Publicado: (2023)

Expression of schizophrenia biomarkers in extraocular muscles from patients with strabismus: an explanation for the link between exotropia and schizophrenia?
por: Agarwal, Andrea B., et al.
Publicado: (2017)

Homozygosity Mapping and Targeted Sanger Sequencing Reveal Genetic Defects Underlying Inherited Retinal Disease in Families from Pakistan
por: Maria, Maleeha, et al.
Publicado: (2015)

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa
por: Azam, Maleeha, et al.
Publicado: (2009)

Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld‐Rieger syndrome
por: Lo Faro, Valeria, et al.
Publicado: (2020)

Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome
por: Ajmal, Muhammad, et al.
Publicado: (2013)

Association of Pro12Ala polymorphism in peroxisome proliferator activated receptor gamma with proliferative diabetic retinopathy
por: Tariq, Khadija, et al.
Publicado: (2013)

Polymorphisms in matrix metalloproteinases MMP1 and MMP9 are associated with primary open-angle and angle closure glaucoma in a Pakistani population
por: Micheal, Shazia, et al.
Publicado: (2013)

Anisometropia and refractive status in children with unilateral congenital nasolacrimal duct obstruction
por: Saleem, Adnan Aslam, et al.
Publicado: (2018)

Exotropía
por: Sánchez Hernández, Norma Leticia
Publicado: (1994)

Exotropia/
por: Sánchez Hernández Norma Leticia
Publicado: (1994)

XRCC1 and XPD DNA repair gene polymorphisms: A potential risk factor for glaucoma in the Pakistani population
por: Yousaf, Sajeela, et al.
Publicado: (2011)

Association of known common genetic variants with primary open angle, primary angle closure, and pseudoexfoliation glaucoma in Pakistani cohorts
por: Micheal, Shazia, et al.
Publicado: (2014)

Role of ACE and PAI-1 Polymorphisms in the Development and Progression of Diabetic Retinopathy
por: Saleem, Saba, et al.
Publicado: (2015)

Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosa
por: Ajmal, Muhammad, et al.
Publicado: (2012)

Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
por: Micheal, Shazia, et al.
Publicado: (2016)

GABRG2 C588T Polymorphism Is Associated with Idiopathic Generalized Epilepsy but Not with Antiepileptic Drug Resistance in Pakistani Cohort
por: Saleem, Tayyaba, et al.
Publicado: (2022)

Type of the recurrent exotropia after bilateral rectus recession for intermittent exotropia
por: Cho, Kwan Hyuk, et al.
Publicado: (2016)

A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease
por: Waheed, Nadia K., et al.
Publicado: (2012)

Association of Interleukin-6 Gene Promoter Polymorphism with Coronary Artery Disease in Pakistani Families
por: Satti, Humayoon Shafiq, et al.
Publicado: (2013)

Management of Consecutive Exotropia
por: Rajavi, Zhale, et al.
Publicado: (2022)

The subjective controllability of exotropia and its effect on surgical outcomes in patients with intermittent exotropia
por: Kim, Mirae, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_349s9u84o5vfl2rul6ehr5hflr