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[Hereditary cerebro-oculo-renal syndromes]. / Arvelige cerebrookulorenale syndrome.
Sessa, Galina; Hjortshøj, Tina Duelund; Egfjord, Martin.
Afiliação
  • Sessa G; Nefrologisk klinik P, Rigshospitalet, Blegdamsvej 9, 2100 København Ø. sessa.mg@gmail.com.
Ugeskr Laeger ; 176(8A): V07130452, 2014 Feb 17.
Article em Da | MEDLINE | ID: mdl-25350305
Although many congenital diseases present disturbances of the central nervous system, eyes and renal function, only few of these have a defined genetic basis. The first clinical features of cerebro-oculo-renal diseases usually develop in early childhood and deterioration of kidney function and even end-stage kidney disease may occur in a young age. The syndromes should be considered in patients with retarded growth and development, central nervous system abnormalities, impaired vision or blindness and progressive renal failure.
Assuntos
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Base de dados: MEDLINE Assunto principal: Síndrome Oculocerebrorrenal Idioma: Da Ano de publicação: 2014 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Síndrome Oculocerebrorrenal Idioma: Da Ano de publicação: 2014 Tipo de documento: Article