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Last Updated: 10/31/2025

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Found 13 publications

Congenital Microcoria: Clinical Features and Molecular Genetics.

Congenital Microcoria: Clinical Features and Molecular Genetics.

Journal: Genes
Published: March 10, 2021

Congenital Microcoria.

Congenital Microcoria.

Journal: Ophthalmology
Published: October 08, 2020

Microcoria due to first duplication of 13q32.1 including the GPR180 gene and maternal mosaicism.

Microcoria due to first duplication of 13q32.1 including the GPR180 gene and maternal mosaicism.

Journal: European journal of medical genetics
Published: December 28, 2019

Congenital microcoria in a Saudi family.

Congenital microcoria in a Saudi family.

Journal: Ophthalmic genetics
Published: November 23, 2019

Miosis in a case of congenital fibrosis of extraocular muscles: a rare presentation of a rare disease.

Miosis in a case of congenital fibrosis of extraocular muscles: a rare presentation of a rare disease.

Journal: BMJ case reports
Published: March 23, 2019

Phacoemulsification and 1% atropine eye drops for treatment of antimetropic congenital microcoria associated with cataracts.

Phacoemulsification and 1% atropine eye drops for treatment of antimetropic congenital microcoria associated with cataracts.

Journal: Arquivos brasileiros de oftalmologia
Published: July 24, 2018

Acorea: A rare congenital anomaly.

Acorea: A rare congenital anomaly.

Journal: Indian journal of ophthalmology
Published: February 27, 2018

Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood-onset glaucoma.

Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood-onset glaucoma.

Journal: Acta ophthalmologica
Published: September 29, 2016

A novel gain-of-function mutation in ORAI1 causes late-onset tubular aggregate myopathy and congenital miosis.

A novel gain-of-function mutation in ORAI1 causes late-onset tubular aggregate myopathy and congenital miosis.

Journal: Clinical genetics
Published: August 12, 2016

Submicroscopic deletions at 13q32.1 cause congenital microcoria.

Submicroscopic deletions at 13q32.1 cause congenital microcoria.

Journal: American journal of human genetics
Published: October 08, 2014

Familial acorea, microphthalmia and cataract syndrome.

Familial acorea, microphthalmia and cataract syndrome.

Journal: The British journal of ophthalmology
Published: July 09, 2013

Seizure-induced miosis.

Seizure-induced miosis.

Journal: Epilepsia
Published: November 05, 2011
Showing 1-12 of 13

Last Updated: 10/31/2025