Macular corneal dystrophy

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Macular corneal dystrophy
Macular corneal dystrophy hale colloidal iron stain.JPEG
Colloidal iron staining shows deposition of glycosaminoglycans in the cornea
Classification and external resources
ICD-10 Xxx.x
ICD-9-CM xxx

Macular corneal dystrophy, also known as Fehr corneal dystrophy named for German ophthalmologist Oskar Fehr (1871-1959), is a rare pathological condition affecting the stroma of cornea. The first signs are usually noticed in the first decade of life, and progress afterwards, with opacities developing in the cornea and attacks of pain. The condition was first described by Arthur Groenouw in 1890.[1][2]

Signs and symptoms[edit]

Onset occurs in the first decade, usually between ages 5 and 9. The disorder is progressive. Minute, gray, punctate opacities develop. Corneal sensitivity is usually reduced. Painful attacks with photophobia, foreign body sensations, and recurrent erosions occur in most patients. Macular corneal dystrophy is very common in Iceland and accounts for almost one-third of all corneal grafts performed there.[3]

Genetics[edit]

Macular corneal dystrophy is inherited in autosomal recessive fashion and is thought to be caused by the lack or abnormal configuration of keratan sulfate. Most cases of MCD are caused by mutations in CHST6 gene.[4]

The gene CHST6 is a carbohydrate sulfotransferase encoding an enzyme designated corneal N-acetylglucosamine-6-sulfotransferase. In MCD type I, various mutations lead to inactivation of the enzyme, in MCD type II, inactivation is caused by large deletions and/or replacements in the gene.[3]

Treatment[edit]

Corneal transplantation is often required.

See also[edit]

References[edit]

  1. ^ Groenouw A. Knötchenförmige Hornhauttrübungen (noduli corneae). Arch Augenheilkunde. 1890;21:281–289.
  2. ^ Natalie Afshari. "Macular corneal dystrophy". eMedicine. 
  3. ^ a b Online Mendelian Inheritance in Man (OMIM) 217800
  4. ^ Klintworth GK (2009). "Corneal dystrophies". Orphanet J Rare Dis. 4: 7. doi:10.1186/1750-1172-4-7. PMC 2695576Freely accessible. PMID 19236704.