Neuroferritinopathy: missense mutation in FTL causing early-onset bilateral pallidal involvement.

Article Details

Citation

Maciel P, Cruz VT, Constante M, Iniesta I, Costa MC, Gallati S, Sousa N, Sequeiros J, Coutinho P, Santos MM

Neuroferritinopathy: missense mutation in FTL causing early-onset bilateral pallidal involvement.

Neurology. 2005 Aug 23;65(4):603-5.

PubMed ID
16116125 [ View in PubMed
]
Abstract

The authors identified a missense mutation in the FTL gene (474G>A; A96T) in a 19-year-old man with parkinsonism, ataxia, corticospinal signs, mild nonprogressive cognitive deficit, and episodic psychosis. This mutation was also present in his asymptomatic mother and younger brother, who had abnormally low levels of ferritin in the serum. The patient and his mother displayed bilateral involvement of the pallidum.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Ferritin light chainP02792Details