Cornea plana 2

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Cornea plana 2
Other namesAutosomal recessive Cornea plana, CNA2.
autosomal recessive manner.
SpecialtyMedical genetics Edit this on Wikidata

Cornea plana 2 (CNA2) is a

autosomal recessive disorder.[4]

Signs and symptoms

Cornea plana commonly presents as a flat cornea, early-onset arcus lipoides, low anterior chamber depth, and an indistinct border between the sclera and cornea due to a decreased angle between the two.[2] Although a small corneal diameter is anticipated, measuring it can be challenging because the scleral tissue overlaps the cornea by a few millimeters. In the patients who have cornea plana, the anterior chamber depth has been found to vary from 0.8 to 2.1 mm.[5]

Moreover, high

hyperopia, myopia has been identified in a few cases.[7] As many as 90 percent of cases have a bilateral presentation, which is linked to sclerocornea.[1] Finally, congenital ptosis has also been reported, and the absence of corneal protrusion is most likely the cause.[5]

Diagnosis

Clinical presentation, keratometry,[7] pachymetry, and endothelial imaging are used to make the diagnosis.[8]

Since the decreased refraction in the autosomal recessive form is more severe than in the autosomal dominant form, corneal refraction measurements can be used to differentiate between CNA1 and CNA2.[5]

Histology is distinguished by

Bowman's membrane defects, and stromal vascularization and scar formation.[4]

See also

References

Further reading

External links