Leukoencephalopathy, intracranial calcifications, and cysts (LCC) is a very rare cerebral disorder, first described in 3 children in 1996. It has subsequently been reported in adults and children from Europe and America, but has not so far been reported from Asia. We report an adult patient with pathologically proven LCC from a tertiary care hospital in South India. He presented with features of ataxia and raised intracranial pressure. Magnetic resonance imaging of the brain showed multiple bilateral cerebral cystic lesions along with diffuse white matter lesions in the cerebral and cerebellar white matter, and computed tomography of brain showed multiple calcifications in the white matter and basal ganglia. A large right cerebellar cyst ca...
Extensive intracranial calcifications and leukoencephalopathy are seen in both Coats plus and leukoe...
We present a clinical, neuro-radiological and genetic study on a family with members suffering from ...
Labrune’s syndrome, or leukoencephalopathy with brain calcifications and cysts (LCC), is a rare gene...
Association of leukoencephalopathy, cerebral calcifications, and cysts (LCC) is a rare disorder that...
Although basal ganglia calcifications were described a long time ago,1,3,11 the association of leuko...
Background: Leukoencephalopathy with cerebral calcifications and cysts (LCC) is a recently described...
The association of leukoencephalopathy with cerebral cal-cifications and cysts (LCC), Labrune syndro...
Objective With the identification of mutations in the conserved telomere maintenance component 1 (CT...
Objective With the identification of mutations in the conserved telomere maintenance component 1 (CT...
Leukoencephalopathy with calcifications and cysts (LCC) is a neurological syndrome recently associat...
Abstract Background Leukoencephalopathy with brain ca...
The patient is a 20-year-old woman with an unremarkable family history who began to have focal seizu...
Leukoencephalopathy, cerebral calcifications, and cysts (LCC) form a very rare association which is ...
Syndrome is characterized by cerebral calcification andcyst formation (CRMCC), as defined in recent ...
A 37-year-old man was referred for a 1-year history of word naming difficulties and progressive exec...
Extensive intracranial calcifications and leukoencephalopathy are seen in both Coats plus and leukoe...
We present a clinical, neuro-radiological and genetic study on a family with members suffering from ...
Labrune’s syndrome, or leukoencephalopathy with brain calcifications and cysts (LCC), is a rare gene...
Association of leukoencephalopathy, cerebral calcifications, and cysts (LCC) is a rare disorder that...
Although basal ganglia calcifications were described a long time ago,1,3,11 the association of leuko...
Background: Leukoencephalopathy with cerebral calcifications and cysts (LCC) is a recently described...
The association of leukoencephalopathy with cerebral cal-cifications and cysts (LCC), Labrune syndro...
Objective With the identification of mutations in the conserved telomere maintenance component 1 (CT...
Objective With the identification of mutations in the conserved telomere maintenance component 1 (CT...
Leukoencephalopathy with calcifications and cysts (LCC) is a neurological syndrome recently associat...
Abstract Background Leukoencephalopathy with brain ca...
The patient is a 20-year-old woman with an unremarkable family history who began to have focal seizu...
Leukoencephalopathy, cerebral calcifications, and cysts (LCC) form a very rare association which is ...
Syndrome is characterized by cerebral calcification andcyst formation (CRMCC), as defined in recent ...
A 37-year-old man was referred for a 1-year history of word naming difficulties and progressive exec...
Extensive intracranial calcifications and leukoencephalopathy are seen in both Coats plus and leukoe...
We present a clinical, neuro-radiological and genetic study on a family with members suffering from ...
Labrune’s syndrome, or leukoencephalopathy with brain calcifications and cysts (LCC), is a rare gene...