Kei Shinoda Department of Brain and Neuroscience Division of Sensory and Locomotive Science, Ophthalmology Oita University Faculty of. PubMed journal article Presumed solitary circumscribed retinal astrocytic proliferatio were found in PRIME PubMed. Download Prime PubMed App to iPhone or. Angio-OCT en hamartoma astrocíticos retiniano solitario Astrocitoma subependimario de células gigantes en el complejo de esclerosis tuberosa.

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De excrescentals verrucosa cristois in intestinis crassis astroccitoma passi observatis. La esclerosis tuberosa tiene una incidencia de 1 cada Sulindac for periampullary polyps in FAP patients.

Subscribe to our Newsletter. Optical coherence tomography showed the mass with a snowball configuration and a smooth surface. Glial tumor of the retina.

Hamartoma retiniano en esclerosis tuberosa

World J Surg ; Relationship between APC genotype, polyp distribution, and oral sulindac treatment in the colon and rectum of patients with familial adenomatous polyposis. Autofluorescence disclosed moderate hyperautofluorescence.


Are you a health professional able to prescribe or dispense drugs? Ultrasound showed no calcification.

The King Khaled Memorial Lecture. Familial polyposis coli; family studies, histopathology, differential diagnosis and results of treatment.

Lal G, Gallinger S. Presumed solitary circumscribed retinal astrocytic proliferation. Epidermoid cysts, polyposis coli and Gardner’s syndrome.

Hamartoma retiniano en esclerosis tuberosa – PDF Free Download

The genomic landscape of tuberous sclerosis complex. Other extracolonic manifestations were represented by upper digestive adenomas, epidermoid cysts, desmoid tumor seven eachgastric cancer three and tireoid cancer two.

Desmoid tumors in familial adenomatous polyposis. Isolated, unilateral astrocytic hamartomas found in healthy individuals usually occur spontaneously.

[Retinal hamartoma in tuberous sclerosis]. – PDF Download Free

TSC is an autosomal dominant, multisystem disorder connected to aberrant regulation. Predictive value of congenital hypertrophy of the retinal pigment epithelium as a clinical marker for familial adenomatous polyposis.

Despite the isolated single nature of the astrocytic hamartoma in this case, given that this is a rare condition and there are potential systemic associations, referral to a retinal specialist for confirmation of diagnosis and management is recommended. Malignant renal angiomyolipoma without tuberous sclerosis.


Am J Genet ;3: The tuberous sclerosis complex gets fatter. Br J Ophthalmol ; Eur J Hum Genet ;8: Familial risk and colorectal cancer [review].

SNIP measures contextual citation impact by wighting citations based on the refiniano number of citations in a subject field. Am J Ophthalmol ; Aggressive retinal astrocytomas in patients with tuberous sclerosis complex. Incidence and predictive value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients. Sem Colon Rectal Surg ;2: