Descemet's membrane

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Descemet's membrane
Vertical section human cornea-Gray871.png
Vertical section of human cornea from near the margin. (Waldeyer.) Magnified.
  1. Epithelium
  2. Anterior elastic lamina
  3. substantia propria
  4. Posterior elastic lamina.
    (Descemet's membrane)
  5. Endothelium of the anterior chamber
  1. Oblique fibers in the anterior layer of the substantia propria
  2. Lamellae, the fibers of which are cut across, producing a dotted appearance
  3. Corneal corpuscles appearing fusiform in section
  4. Lamellae, the fibers of which are cut longitudinally
  5. Transition to the sclera, with more distinct fibrillation, and surmounted by a thicker epithelium
  6. Small blood vessels cut across near the margin of the cornea
Details
PronunciationEnglish: /ˈdɛsəm/
Location Cornea of eye
Identifiers
Latin l. limitans posterior corneae
MeSH D003886
TA98 A15.2.02.021
FMA 58309
Anatomical terms of microanatomy

Descemet's membrane (or the Descemet membrane) is the basement membrane that lies between the corneal proper substance, also called stroma, and the endothelial layer of the cornea. It is composed of different kinds of collagen (Type IV and VIII) [1] than the stroma. The endothelial layer is located at the posterior of the cornea. Descemet's membrane, as the basement membrane for the endothelial layer, is secreted by the single layer of squamous epithelial cells that compose the endothelial layer of the cornea.

Contents

Structure

Its thickness ranges from 3 μm at birth to 8–10 μm in adults. [2]

The corneal endothelium is a single layer of squamous cells covering the surface of the cornea that faces the anterior chamber.

Clinical significance

Copper disposition on corneal Descemet's membrane KF ring 2.jpg
Copper disposition on corneal Descemet's membrane

Significant damage to the membrane may require a corneal transplant. Damage caused by the hereditary condition known as Fuchs dystrophy (q.v.)—where Descemet's membrane progressively fails and the cornea thickens and clouds because the exchange of nutrients/fluids between the cornea and the rest of the eye is interrupted—can be reversed by surgery. The surgeon can scrape away the damaged Descemet membrane and insert/transplant a new membrane harvested from the eye of a donor. [3] In the process most of the squamous cells of the donor membrane survive to dramatically and emphatically reverse the corneal deterioration (see DMEK surgery).

Descemet's membrane is also a site of copper deposition in patients with Wilson's disease or other liver diseases, leading to formation of Kayser–Fleischer rings.

History

It is also known as the posterior limiting elastic lamina, lamina elastica posterior, and membrane of Demours. It was named after French physician Jean Descemet (1732–1810).

See also

Related Research Articles

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<span class="mw-page-title-main">Cornea</span> Transparent front layer of the eye

The cornea is the transparent front part of the eye that covers the iris, pupil, and anterior chamber. Along with the anterior chamber and lens, the cornea refracts light, accounting for approximately two-thirds of the eye's total optical power. In humans, the refractive power of the cornea is approximately 43 dioptres. The cornea can be reshaped by surgical procedures such as LASIK.

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The Bowman's layer is a smooth, acellular, nonregenerating layer, located between the superficial epithelium and the stroma in the cornea of the eye. It is composed of strong, randomly oriented collagen fibrils in which the smooth anterior surface faces the epithelial basement membrane and the posterior surface merges with the collagen lamellae of the corneal stroma proper.

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The corneal endothelium is a single layer of endothelial cells on the inner surface of the cornea. It faces the chamber formed between the cornea and the iris.

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Fuchs dystrophy, also referred to as Fuchs endothelial corneal dystrophy (FECD) and Fuchs endothelial dystrophy (FED), is a slowly progressing corneal dystrophy that usually affects both eyes and is slightly more common in women than in men. Although early signs of Fuchs dystrophy are sometimes seen in people in their 30s and 40s, the disease rarely affects vision until people reach their 50s and 60s.

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<span class="mw-page-title-main">Corneal hydrops</span> Medical condition

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References

  1. "Tissue Distribution of Type VIII Collagen in Human Adult and Fetal Eyes" (PDF). Investigative Ophthalmology and Visual Science. 1991-08-01. Retrieved 2014-08-17.
  2. Johnson DH, Bourne WM, Campbell RJ: The ultrastructure of Descemet's membrane. I. Changes with age in normal cornea. Arch Ophthalmol 100:1942, 1982
  3. Stuart AJ, Virgili G, Shortt AJ (2016). "Descemet's membrane endothelial keratoplasty versus Descemet's stripping automated endothelial keratoplasty for corneal endothelial failure". Cochrane Database Syst Rev (3): CD012097. doi: 10.1002/14651858.CD012097 .

Histology A text and atlas. Michael H.Ross and Wojciech Pawlina 5th Edition 2006