The pathogenesis of retinal dysplasia.

نویسندگان

  • A M Silverstein
  • B I Osburn
  • R A Prendergast
چکیده

The term retinal dysplasia has been em­ ployed with two connotations in the ophthal­ mic literature. Its early usewas the more general, referring to abnormalities in the histogenesis of the developing retina. The term was used more restrictively by Reese and Blodi and Reese and Straatsma to desig­ nate a specific syndrome consisting of multi­ ple congenital anomalies, including bilateral ocular abnormalities, presenting a more or less typical histopathologic picture. The wide­ spread application of karyologic analysis during the past decade has made it clear that most of the cases of this syndrome described by Reese and coworkers' were probably re­ lated to a trisomy in the D group of chromo­ somes (13-15 trisomy).

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Ocular abnormalities in the myopathic hamster (UM-X7.1 strain).

Eyes from cardiomyopathic hamsters (UM-X7.1 strain) were examined histologically for evidence of ocular defects. Changes observed included microphthalmia, scleral ectasia, scleral rupture, keratoconus, retinal detachment, retinal dysplasia, retinal fragmentation, retinal thinning, fibrosis of iris and ciliary body, ectopia lentis, and cataract formation. Lesions characteristic of cardiomyopathi...

متن کامل

گزارش یک مورد سندروم نادر Susac از بخش نورولوژی بیمارستان امام خمینی، سال 1378

This syndrome is a very rare neurological presentation which was first reported by Susac in 1975, and usually involves the young women with triad of: (1) Visual loss due to occlusion of retinal artery branches. (2) Subacute encephalopathy with psychic manifestation, personality disorders, involvement of the cortico-spianal tracts, pseudo-bulbar, focal or generalized seizures and myoclonic jerks...

متن کامل

معرفی یک بیمار مبتلا به Giant cell tumor استخوان کشکک همراه با متاستازی ریوی

This syndrome is a very rare neurological presentation which was first reported by Susac in 1975, and usually involves the young women with triad of: (1) Visual loss due to occlusion of retinal artery branches. (2) Subacute encephalopathy with psychic manifestation, personality disorders, involvement of the cortico-spianal tracts, pseudo-bulbar, focal or generalized seizures and myoclonic jerks...

متن کامل

Origin of fundus hyperautofluorescent spots and their role in retinal degeneration in a mouse model of Goldmann-Favre syndrome

Goldmann-Favre syndrome, also known as enhanced S-cone syndrome, is an inherited retinal degeneration disease in which a gain of photoreceptor cell types results in retinal dysplasia and degeneration. Although microglia have been implicated in the pathogenesis of many neurodegenerative diseases, the fundamental role of these cells in this disease is unknown. In the current study, sequential ana...

متن کامل

Differential mitochondrial DNA and gene expression in inherited retinal dysplasia in miniature Schnauzer dogs.

PURPOSE To investigate the molecular basis of inherited retinal dysplasia in miniature Schnauzers. METHODS Retina and retinal pigment epithelial tissues were collected from canine subjects at the age of 3 weeks. Total RNA isolated from these tissues was reverse transcribed to make representative cDNA pools that were compared for differences in gene expression by using a subtractive hybridizat...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • American journal of ophthalmology

دوره 72 1  شماره 

صفحات  -

تاریخ انتشار 1971