Cataract-microcornea syndrome

Cataract-microcornea syndrome
	Autosomal dominant - en.svg
	Cataract-microcornea syndrome is inherited in an autosomal dominant manner ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ;

The cataract-microcornea syndrome is the association of congenital cataract and microcornea.

Genetics[edit]

Mutations in ABCA3 were found to be associated to this syndrome.^[2]

Diagnosis[edit]

Treatment[edit]

References[edit]

↑ OMIM Entry - # 116200 - CATARACT 1, MULTIPLE TYPES; CTRCT1(link). omim.org.
↑ "Mutations in the ABCA3 gene are associated with cataract-microcornea syndrome".Investigative Ophthalmology & Visual Science.2014;55
8031–43.doi:10.1167/iovs.14-14098.PMID:25406294.

External links[edit]

This article about an ophthalmic disease is a stub. You can help WikiMD by expanding the page.

Cataract-microcornea syndrome[edit]

Diagram illustrating autosomal dominant inheritance pattern.

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[1] OMIM Entry - # 116200 - CATARACT 1, MULTIPLE TYPES; CTRCT1(link). omim.org.

[2] "Mutations in the ABCA3 gene are associated with cataract-microcornea syndrome".Investigative Ophthalmology & Visual Science.2014;55
8031–43.doi:10.1167/iovs.14-14098.PMID:25406294.

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