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[Corneal disorders in Wilson's disease].
Orv Hetil 2019; 160(14):555-557OH

Abstract

Wilson's disease is an autosomal recessive hereditary metabolic disease with a pathological accumulation of copper in tissues. This study presents the case of a family, where two females and one male from among six siblings had this disease. While in the case of the two women only the liver was affected, the young man presented with both psychiatric and ophthalmic disorders. Modern examination methods (anterior segment optical coherence tomography, corneal topography, endothelial specular microscopy) were used to gather data on the corneal disorder that manifested with the classic Kayser-Fleischer ring. We underline the importance of ophthalmological checkup which may help to diagnose this disease. Orv Hetil. 2019; 160(14): 555-557.

Authors+Show Affiliations

Szemészeti Osztály, Kenézy Gyula Egyetemi Oktató Kórház Debrecen, Bartók Béla u. 2-26., 4031.Szemészeti Osztály, Kenézy Gyula Egyetemi Oktató Kórház Debrecen, Bartók Béla u. 2-26., 4031.Szemészeti Tanszék, Debreceni Egyetem, Általános Orvostudományi Kar Debrecen.

Pub Type(s)

English Abstract
Journal Article

Language

hun

PubMed ID

30931597

Citation

Sohajda, Zoltán, et al. "[Corneal Disorders in Wilson's Disease]." Orvosi Hetilap, vol. 160, no. 14, 2019, pp. 555-557.
Sohajda Z, Hódos M, Módis L. [Corneal disorders in Wilson's disease]. Orv Hetil. 2019;160(14):555-557.
Sohajda, Z., Hódos, M., & Módis, L. (2019). [Corneal disorders in Wilson's disease]. Orvosi Hetilap, 160(14), pp. 555-557. doi:10.1556/650.2019.31363.
Sohajda Z, Hódos M, Módis L. [Corneal Disorders in Wilson's Disease]. Orv Hetil. 2019;160(14):555-557. PubMed PMID: 30931597.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Corneal disorders in Wilson's disease]. AU - Sohajda,Zoltán, AU - Hódos,Márta, AU - Módis,László, PY - 2019/4/2/entrez KW - Wilson-kór KW - Wilson’s disease KW - anterior segment optical coherence tomography KW - az elülső szegmentum optikaikoherencia-tomográfiája KW - pachymetry KW - szaruhártya-vastagság SP - 555 EP - 557 JF - Orvosi hetilap JO - Orv Hetil VL - 160 IS - 14 N2 - Wilson's disease is an autosomal recessive hereditary metabolic disease with a pathological accumulation of copper in tissues. This study presents the case of a family, where two females and one male from among six siblings had this disease. While in the case of the two women only the liver was affected, the young man presented with both psychiatric and ophthalmic disorders. Modern examination methods (anterior segment optical coherence tomography, corneal topography, endothelial specular microscopy) were used to gather data on the corneal disorder that manifested with the classic Kayser-Fleischer ring. We underline the importance of ophthalmological checkup which may help to diagnose this disease. Orv Hetil. 2019; 160(14): 555-557. SN - 1788-6120 UR - https://www.unboundmedicine.com/medline/citation/30931597/[Corneal_disorders_in_Wilson's_disease] L2 - http://www.akademiai.com/doi/full/10.1556/650.2019.31363?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub=pubmed DB - PRIME DP - Unbound Medicine ER -