نتایج جستجو برای: neuroacanthocytosis

تعداد نتایج: 95  

Journal: :Current opinion in hematology 2014
Lucia De Franceschi Giel J C G M Bosman Narla Mohandas

PURPOSE OF REVIEW This review discusses the mechanisms involved in the generation of thorny red blood cells (RBCs), known as acanthocytes, in patients with neuroacanthocytosis, a heterogenous group of neurodegenerative hereditary disorders that include chorea-acanthocytosis (ChAc) and McLeod syndrome (MLS). RECENT FINDINGS Although molecular defects associated with neuroacanthocytosis have be...

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 2014

Journal: :International Journal of Case Reports and Images 2013

Journal: :iranian journal of neurology 0
mohammad rohani department of neurology, school of medicine, rasoul akram hospital, iran university of medical sciences, tehran, iran. gholamali shahidi department of neurology, school of medicine, rasoul akram hospital, iran university of medical sciences, tehran, iran.

no abstract

Journal: :Annals of neurology 2001
A Danek J P Rubio L Rampoldi M Ho C Dobson-Stone F Tison W A Symmans M Oechsner W Kalckreuth J M Watt A J Corbett H H Hamdalla A G Marshall I Sutton M T Dotti A Malandrini R H Walker G Daniels A P Monaco

McLeod syndrome is caused by mutations of XK, an X-chromosomal gene of unknown function. Originally defined as a peculiar Kell blood group variant, the disease affects multiple organs, including the nervous system, but is certainly underdiagnosed. We analyzed the mutations and clinical findings of 22 affected men, aged 27 to 72 years. Fifteen different XK mutations were found, nine of which wer...

2007
R. H. Walker

Neuroacanthocytosis syndromes are characterized by the presence of “thorny” red blood cells and neurodegeneration of the basal ganglia, along with peripheral neuromuscular findings, seizures, and a variety of neuropsychiatric features. In recent years significant progress has been made in understanding the molecular pathophysiology of these disorders; cases are now identified as autosomal reces...

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