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Cornea plana 1 information


Cornea plana 1
Other namesAutosomal Dominant Cornea Plana, CNA1.
Cornea plana 1 is inherited in an autosomal dominant manner.
SpecialtyOphthalmology

Cornea plana 1 (CNA1) is a congenital disorder that causes the cornea to flatten and the angle between the sclera and cornea to shrink.[1] This could result in the early development of arcus lipoides, hazy corneal limbus, and hyperopia.[2] Cornea plana 1 is an autosomal dominant disorder.[3]

  1. ^ Sutton, Gerard; Lawless, Michael A; Rogers, Christopher M (1995). "Cornea plana". Australian and New Zealand Journal of Ophthalmology. 23 (1). Wiley: 74–75. doi:10.1111/j.1442-9071.1995.tb01651.x. ISSN 0814-9763. PMID 7619462.
  2. ^ Tahvanainen, E; Forsius, H; Kolehmainen, J; Damsten, M; Fellman, J; de la Chapelle, A (February 1, 1996). "The genetics of cornea plana congenita". Journal of Medical Genetics. 33 (2). BMJ: 116–119. doi:10.1136/jmg.33.2.116. ISSN 1468-6244. PMC 1051836. PMID 8929947.
  3. ^ Forsius, Henrik; Damsten, Margareta; Eriksson, Aldur W.; Fellman, Johan; Lindh, Sinikka; Tahvanainen, Esa (1998). "Autosomal recessive cornea plana. A clinical and genetic study of 78 cases in Finland". Acta Ophthalmologica Scandinavica. 76 (2). Wiley: 196–203. doi:10.1034/j.1600-0420.1998.760215.x. ISSN 1395-3907. PMID 9591953.

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