Niemman Pick type C (NPC) is a treatable neurodegenerative lysosomal disorder characterized by the widespread age of onset and clinical presentation. The adult NPC phenotype frequently includes ataxia, supranuclear gaze palsy, and cognitive and behavioral problems.1 Movement disorders are also often observed in these patients. Among them, chorea has been rarely described as a dominant sign.1, 2 On the other hand, a phenotype dominated by chorea and cognitive and behavioral manifestations is suggestive of Huntington's disease (HD).3, 4 The rare cases showing this phenotype proved to be negative for the CAG expansion in HTT and are categorized as Huntington-like disorders (HDL).5 Although the list of HDL genetic etiologies has grown considera...
INTRODUCTION: Chorea-acanthocytosis (ChAc) and Huntington's disease (HD) are neurodegenerative condi...
BACKGROUND Chorea may be present in a number of diseases including hereditary disorders. Major ad...
BACKGROUND: Niemann-Pick Disease Type C (NPC) is an autosomal recessive rare disease characterised b...
NKX2-1 mutations have been usually associated with a non-progressive neurological disease. Recent re...
Background: Niemann-Pick disease type C (NPC) is a lysosomal storage disease caused by mutations in ...
The presence of peripheral blood film acanthocytes can help narrow the differential diagnosis of a f...
Copyright © 2014 Raul E. Piña-Aguilar et al. This is an open access article distributed under the C...
The presence of peripheral blood film acanthocytes can help narrow the differential diagnosis of a f...
The early onset of gait akinesia should not rule out the diagnosis of hereditary chorea. It would be...
Chorea can be caused by a multitude of etiologies: neurodegenerative, pharmacological, structural, m...
Niemann-Pick disease type C is a rare hereditary disorder caused by mutation-disrupted metabolism of...
Copyright © 2015 Ryo Suzuki et al. This is an open access article distributed under the Creative Com...
BACKGROUND : Niemann-Pick disease type C (NP-C) is a rare, inherited neurodegenerative disease of im...
Background Niemann-Pick disease type C (NP-C) is a rare autosomal recessive disorder of lysosomal ch...
Differential diagnosis of familial chorea encompasses Huntington’s disease along with a group of co...
INTRODUCTION: Chorea-acanthocytosis (ChAc) and Huntington's disease (HD) are neurodegenerative condi...
BACKGROUND Chorea may be present in a number of diseases including hereditary disorders. Major ad...
BACKGROUND: Niemann-Pick Disease Type C (NPC) is an autosomal recessive rare disease characterised b...
NKX2-1 mutations have been usually associated with a non-progressive neurological disease. Recent re...
Background: Niemann-Pick disease type C (NPC) is a lysosomal storage disease caused by mutations in ...
The presence of peripheral blood film acanthocytes can help narrow the differential diagnosis of a f...
Copyright © 2014 Raul E. Piña-Aguilar et al. This is an open access article distributed under the C...
The presence of peripheral blood film acanthocytes can help narrow the differential diagnosis of a f...
The early onset of gait akinesia should not rule out the diagnosis of hereditary chorea. It would be...
Chorea can be caused by a multitude of etiologies: neurodegenerative, pharmacological, structural, m...
Niemann-Pick disease type C is a rare hereditary disorder caused by mutation-disrupted metabolism of...
Copyright © 2015 Ryo Suzuki et al. This is an open access article distributed under the Creative Com...
BACKGROUND : Niemann-Pick disease type C (NP-C) is a rare, inherited neurodegenerative disease of im...
Background Niemann-Pick disease type C (NP-C) is a rare autosomal recessive disorder of lysosomal ch...
Differential diagnosis of familial chorea encompasses Huntington’s disease along with a group of co...
INTRODUCTION: Chorea-acanthocytosis (ChAc) and Huntington's disease (HD) are neurodegenerative condi...
BACKGROUND Chorea may be present in a number of diseases including hereditary disorders. Major ad...
BACKGROUND: Niemann-Pick Disease Type C (NPC) is an autosomal recessive rare disease characterised b...