We studied the scientific literature and disease guidelines in order to summarize the clinical utility of the genetic test for Sorsby's fundus dystrophy (SFD). SFD is caused by variations in the TIMP3 gene. Prevalence is, currently unknown. SFD has autosomal dominant inheritance. Clinical diagnosis is based on clinical findings, color vision testing, optical coherence tomography, ophthalmological examination and electroretinography. The genetic test is useful for confirming diagnosis, and for differential diagnosis, couple risk assessment and access to clinical trials
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
Interfamilial phenotypic variations in Sorsby fundus dystrophy (SFD) have given rise to controversy ...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
Sorsby's fundus dystrophy (SFD) has been mapped to a genetic interval of 8 cM between loci D22S275 a...
Sorsby's fundus dystrophy (SFD) is an autosomal dominant macular degeneration developing in the thir...
The hereditary macular dystrophies are progressive degenerations of the central retina and contribut...
Developments in genetics and technology are bringing with them incredible possibilities in the manag...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
Sorsby's fundus dystrophy (SFD) is a rare autosomal dominant macular disorder with age of onset usua...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
Interfamilial phenotypic variations in Sorsby fundus dystrophy (SFD) have given rise to controversy ...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
Sorsby's fundus dystrophy (SFD) has been mapped to a genetic interval of 8 cM between loci D22S275 a...
Sorsby's fundus dystrophy (SFD) is an autosomal dominant macular degeneration developing in the thir...
The hereditary macular dystrophies are progressive degenerations of the central retina and contribut...
Developments in genetics and technology are bringing with them incredible possibilities in the manag...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
Sorsby's fundus dystrophy (SFD) is a rare autosomal dominant macular disorder with age of onset usua...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...