Title |
Contact lens fitting in a patient with Alport syndrome and posterior polymorphous corneal dystrophy: a case report
|
---|---|
Published in |
Arquivos Brasileiros de Oftalmologia, January 2016
|
DOI | 10.5935/0004-2749.20160012 |
Pubmed ID | |
Authors |
Juliana Maria da Silva Rosa, Marcelo Vicente de Andrade, César Lipener |
Abstract |
Alport Syndrome is a hereditary disease that is caused by a gene mutation and affects the production of collagen in basement membranes; this condition causes hemorrhagic nephritis associated with deafness and ocular changes. The X-linked form of this disease is the most common and mainly affects males. Typical ocular findings are dot-and-fleck retinopathy, anterior lenticonus, and posterior polymorphous corneal dystrophy. Some cases involving polymorphous corneal dystrophy and corneal ectasia have been previously described. Here we present a case report of a 33-year-old female with Alport syndrome, posterior polymorphous corneal dystrophy, and irregular astigmatism, whose visual acuity improved with a rigid gas permeable contact lens. |
X Demographics
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 1 | 100% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Practitioners (doctors, other healthcare professionals) | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Brazil | 1 | 4% |
Unknown | 26 | 96% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Bachelor | 6 | 22% |
Student > Doctoral Student | 4 | 15% |
Professor > Associate Professor | 3 | 11% |
Other | 2 | 7% |
Student > Master | 2 | 7% |
Other | 5 | 19% |
Unknown | 5 | 19% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 16 | 59% |
Nursing and Health Professions | 3 | 11% |
Pharmacology, Toxicology and Pharmaceutical Science | 1 | 4% |
Economics, Econometrics and Finance | 1 | 4% |
Agricultural and Biological Sciences | 1 | 4% |
Other | 0 | 0% |
Unknown | 5 | 19% |