Congenital Microcoria Latest Advances

Find the Latest Research About Congenital Microcoria

Last Updated: 02/24/2026

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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: 02/24/2026