Genetics reference · Ophthalmology
Lattice corneal dystrophy type I
MedlinePlus Genetics, National Library of Medicine · Retrieved 2026-10-13
Lattice corneal dystrophy type I is an eye disorder that affects the clear, outer covering of the eye called the cornea. The cornea must remain clear for an individual to see properly; however, in lattice corneal dystrophy type I, protein clumps known as amyloid deposits cloud the cornea, which leads to vision impairment. The cornea is made up of several layers of tissue, and in lattice corneal dystrophy type I, the deposits form in the stromal layer. The amyloid deposits…
Reference details
- Inheritance patterns
- Autosomal dominant
- Other names
- Biber-Haab-Dimmer dystrophy
- NLM review date
- 2012-04
- NLM publication date
- 2020-08-18
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Source date: 2012-04. Retrieved: 2026-10-13. Text has been organized for reading; this import has not been independently reviewed by a clinician. It is not individualized medical advice.
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