Tuberous sclerosis: Ocular manifestations

Angelo Maria Minnella, M. Borgioli, G. Calogero, E. Merendino, B. Bagolini

Risultato della ricerca: Contributo in rivistaArticolo in rivista

Abstract

Tuberous sclerosis is a rare clinical entity, commonly considered as a phakomatosis, characterized by multiple tumors (hamartomas) of the brain, skin, eye and many organs as kidney, heart, spleen and•lung. It is inherited in an irregular authosomal dominant fashion. Ocular findings are multiple retinal astrocytic hamartomas and more rarely non retinal fibrous tumors. Authors consider clinical and diagnostic features of tuberous sclerosis and describe a case of vitreous hemorrhage complicating retinal astrocytic hamartomas
Titolo tradotto del contributo[Autom. eng. transl.] Tuberous sclerosis: Ocular manifestations
Lingua originaleItalian
pagine (da-a)1147-1156
Numero di pagine10
RivistaAnnali di Ottalmologia e Clinica Oculistica
Volume118
Stato di pubblicazionePubblicato - 1992

Keywords

  • Sclerosi tuberosa, malattia di Bourneville, astrocitoma retinico
  • Tuberous sclerosis, Bourneville's disease, retinal astrocytic hamartoma

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