Sandhoff disease is a severe form of GM, gangliosidosis that is caused by the deficiency of both hexosaminidase A and B, Startle reaction, hypotonia, psychomotor retardation, and blindness are the main clinical features. Presented are computed tomography and magnetic resonance imaging findings of four patients with Sandhoff disease diagnosed by enzymatic analyses, Bilateral homogeneous thalamic hyperdensity was evident on computed tomography, Magnetic resonance imaging scans revealed mild cortical atrophy, a thin corpus callosum, and abnormal signal intensities in the caudate nucleus, globus pallidum, putamen, cerebellum, and brainstem, No correlation was evident between the severity of the central nervous system imaging findings and the cl...
BACKGROUND AND PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine...
Sandhoff disease is a lysosomal storage disease caused by a deficiency of beta-hexosaminidase. Affec...
Purpose: Mowat-Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial featur...
Sandhoff disease is a lipid-storage disorder caused by a defect in ganglioside metabolism. It is cau...
A case of GM2 gangliosidosis is reported: the diagnosis has been made by clinical findings showing m...
In 13 patients, the GM2 gangliosidoses, Sandhoff disease and Tay-Sachs disease, were found to be con...
Abstract Background Infantile Sandhoff disease (ISD) is a GM2 gangliosidosis that is classified as a...
Sandhoff disease (SD) is a fatal, autosomal recessive lysosomal storage disease. Mutations in HEXB g...
Sandhoff disease, one of the GM2 gangliosidoses, is a lysosomal storage disorder characterized by th...
Variant B1 is a rare type of GM2 gangliosidosis. Clinically, it shows a wide spectrum of forms rangi...
Late infantile GM1 gangliosidosis is a rare lysosomal disorder characterized by mental deterioration...
A case of juvenile type Sandhoff disease presenting with mental retardation and local panatrophy was...
GM2 gangliosidosis type Sandhoff is caused by a defect of beta-hexosaminidase, an enzyme involved in...
Purpose:Mowat-Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial feature...
BACKGROUND AND PURPOSE: Leukoencephalopathies of unknown origin constitute a considerable problem in...
BACKGROUND AND PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine...
Sandhoff disease is a lysosomal storage disease caused by a deficiency of beta-hexosaminidase. Affec...
Purpose: Mowat-Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial featur...
Sandhoff disease is a lipid-storage disorder caused by a defect in ganglioside metabolism. It is cau...
A case of GM2 gangliosidosis is reported: the diagnosis has been made by clinical findings showing m...
In 13 patients, the GM2 gangliosidoses, Sandhoff disease and Tay-Sachs disease, were found to be con...
Abstract Background Infantile Sandhoff disease (ISD) is a GM2 gangliosidosis that is classified as a...
Sandhoff disease (SD) is a fatal, autosomal recessive lysosomal storage disease. Mutations in HEXB g...
Sandhoff disease, one of the GM2 gangliosidoses, is a lysosomal storage disorder characterized by th...
Variant B1 is a rare type of GM2 gangliosidosis. Clinically, it shows a wide spectrum of forms rangi...
Late infantile GM1 gangliosidosis is a rare lysosomal disorder characterized by mental deterioration...
A case of juvenile type Sandhoff disease presenting with mental retardation and local panatrophy was...
GM2 gangliosidosis type Sandhoff is caused by a defect of beta-hexosaminidase, an enzyme involved in...
Purpose:Mowat-Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial feature...
BACKGROUND AND PURPOSE: Leukoencephalopathies of unknown origin constitute a considerable problem in...
BACKGROUND AND PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine...
Sandhoff disease is a lysosomal storage disease caused by a deficiency of beta-hexosaminidase. Affec...
Purpose: Mowat-Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial featur...