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MRI and ¹H-MRS findings of three patients with Sjögren-Larsson syndrome Síndrome de Sjögren-Larsson: achados à ressonância magnética e espectroscopia de prótons em três pacientes

Sjögren-Larsson syndrome (SLS) is a rare autosomal recessive neurocutaneous disorder caused by deficiency of the microsomal enzyme fatty aldehyde dehydrogenase. Patients present the classical triad of congenital ichthyosis, mental retardation and spastic di- or tetraplegia. Magnetic resonance imagin...

Ausführliche Beschreibung

Gespeichert in:
Bibliografische Detailangaben
Hauptverfasser: Mauro Nakayama, Daniel G.F. Távora, Thereza C.L. Alvim, Alexandre C.B. Araújo, Rômulo L. Gama
Format: Artigo
Sprache:Inglês
Veröffentlicht: Thieme Revinter Publicações 2006-06-01
Schriftenreihe:Arquivos de Neuro-Psiquiatria
Schlagworte:
Online-Zugang:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2006000300009
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