Pseudoxanthoma Elasticum Clinical Trial
Official title:
Evolution of Visual Impairment During Pseudoxanthoma Elasticum
Pseudoxanthoma elasticum is a disease whom frequency is estimated about 1/50000 to 1/100
000. There is a female preponderance with a sex-ratio of 2:1. PXE is transmitted according
either to an autosomal dominant mode or to an autosomal recessive one. Mutations in the
ABCC6 gene on chromosome 16p13.1 have recently been identified causing PXE. The elastic
fibers slowly become mineralized mainly in the skin, the eyes, and the cardiovascular
system. PXE is a multisystem disease that includes a spectrum of clinical manifestations
affecting the skin, the eye or the cardiovascular system as well as other tissues. It can be
responsible for severe and life threatening complications. Skin changes are usually the
first manifestations and begin in early childhood. The vital prognosis of PXE depends on the
severity of the cardiovascular lesions that could be responsible for sudden death in
children and young adults.
Ocular manifestations are quite constant and include chorioretinal scarring, pigmentary
changes or angioid streaks. The natural evolution of the angioid streaks leads to their
enlargement or to the occurrence of subfoveal choroidal neovascularizations and hemorrhages
leaving macular scares. A self-monitoring is recommended since early treatment of subfoveal
CNV is the only way to minimize their pejorative consequences. The gold standard treatment
of the CNV consists in the photocoagulation. New therapeutics has been developed including
photodynamic therapy or intravitreal injection of anti-angiogenic agents and they seems to
be effective to reduce the immediate complications of a limited CNV. This evolution explains
that 50 to 70 % of the patients have a poor vision or legal blindness of one or both eyes.
However, little is known about the age of occurrence of visual impairment in PXE patients.
That is the reason why we decided to review the ophthalmologic status and visual history of
our population of PXE patients according to their age.
A retrospective review of all cases of PXE patients referred by the Department of Genetics
should be performed. This ophthalmologic examination has been conducted as part of the usual
follow up for such PXE patients or for the needs of a treatment of complications of angioid
streaks such as CNV complications.
As we studied the age of poor vision occurrence, we propose to take in account the first
examination when a best-corrected visual acuity (BCVA) under 20/50 was observed. All past
medical events obtains from the data of the patients will be recorded, especially
ophthalmologic ones.
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Observational Model: Cohort, Time Perspective: Retrospective
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