نتایج جستجو برای: leukodystrophy

تعداد نتایج: 2650  

Journal: :Radiographics : a review publication of the Radiological Society of North America, Inc 2002
Jung-Eun Cheon In-One Kim Yong Seung Hwang Ki Joong Kim Kyu-Chang Wang Byung-Kyu Cho Je Geun Chi Chong Jai Kim Woo Sun Kim Kyung Mo Yeon

Dysmyelinating diseases, or leukodystrophies, encompass a wide spectrum of inherited neurodegenerative disorders affecting the integrity of myelin in the brain and peripheral nerves. Most of these disorders fall into one of three categories-lysosomal storage diseases, peroxisomal disorders, and diseases caused by mitochondrial dysfunction-and each leukodystrophy has distinctive clinical, bioche...

Journal: :Einstein 2012
Tatiana Suemi Sano

Krabbe disease (globoid cell leukodystrophy) is an inherited recessive autosomal leukodystrophy caused by deficiency of the enzyme galactocerebrosidase. The lack of this enzyme leads to the build-up of galactolipids that will promote the death of oligodendrocytes and the demyelination of the central and peripheral nervous systems. There are two clinical forms: early onset and late onset. This a...

Journal: :JAMA neurology 2013
Rita Guerreiro Eleanna Kara Isabelle Le Ber Jose Bras Jonathan D Rohrer Ricardo Taipa Tammaryn Lashley Céline Dupuits Nicole Gurunlian Fanny Mochel Jason D Warren Didier Hannequin Frédéric Sedel Christel Depienne Agnès Camuzat Véronique Golfier Foucaud Du Boisguéheneuc Lucia Schottlaender Nick C Fox Jonathan Beck Simon Mead Martin N Rossor John Hardy Tamas Revesz Alexis Brice Henry Houlden

IMPORTANCE The leukodystrophies comprise a clinically and genetically heterogeneous group of progressive hereditary neurological disorders mainly affecting the myelin in the central nervous system. Their onset is variable from childhood to adulthood and presentation can be with a variety of clinical features that include mainly for adult-onset cases cognitive decline, seizures, parkinsonism, mu...

Journal: :Archives of neurology 1995
A T Hageman F J Gabreëls J G de Jong A A Gabreëls-Festen C J van den Berg B A van Oost R A Wevers

OBJECTIVE To determine the clinical symptoms in adult metachromatic leukodystrophy and in adult pseudodeficiency for arylsulfatase A. DESIGN Case series. SETTING University hospital. PATIENTS Twenty-five adult patients with very low arylsulfatase A activity. RESULTS In 13 patients, a diagnosis of adult metachromatic leukodystrophy was made. The main symptoms were dementia, behavioral ab...

2001
Harpreet S. Duggal Vinod K. Sinha S.Haque Nizamie

Leukodystrophies are rare dysmyelinating disorders of the nervous system, which occasionally have an initial psychiatric presentation. This report describes a case of a 9-year-old boy whose initial presentation resembled a bipolar disorder but subsequent work-up revealed an underlying leukodystrophy, most likely Alexander's disease. The course of this rare disease along with the implications of...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1983
P L Chang R G Davidson

Metachromatic leukodystrophy is a hereditary neurodegenerative disorder in man associated with deficient arylsulfatase-A activity (aryl-sulfate sulfohydrolase, EC 3.1.6.1). The same enzyme deficiency has been noted in clinically normal individuals, a condition known as pseudo arylsulfatase-A deficiency. With a nonselective method, somatic cell hybrids were obtained from cultured fibroblasts of ...

2015
Marie Meyer-Ohlendorf Anne Braczynski Omar Al-Qaisi Florian Gessler Saskia Biskup Lutz Weise Joachim P. Steinbach Marlies Wagner Michel Mittelbronn Oliver Bähr

BACKGROUND Hereditary diffuse leukodystrophy with spheroids is a rare type of leukoencephalopathy. Mutations in the colony stimulating factor 1 receptor have recently been identified to be the cause of this microgliopathy. Clinical and radiological presentation can often misguide physicians during the diagnosis of patients with this underdiagnosed disease. CASE PRESENTATION We present a 29 ye...

2015
Isabelle Thiffault Nicole I Wolf Diane Forget Kether Guerrero Luan T Tran Karine Choquet Mathieu Lavallée-Adam Christian Poitras Bernard Brais Grace Yoon Laszlo Sztriha Richard I Webster Dagmar Timmann Bart P van de Warrenburg Jürgen Seeger Alíz Zimmermann Adrienn Máté Cyril Goizet Eva Fung Marjo S van der Knaap Sébastien Fribourg Adeline Vanderver Cas Simons Ryan J Taft John R Yates Benoit Coulombe Geneviève Bernard

A small proportion of 4H (Hypomyelination, Hypodontia and Hypogonadotropic Hypogonadism) or RNA polymerase III (POLR3)-related leukodystrophy cases are negative for mutations in the previously identified causative genes POLR3A and POLR3B. Here we report eight of these cases carrying recessive mutations in POLR1C, a gene encoding a shared POLR1 and POLR3 subunit, also mutated in some Treacher Co...

Journal: :Archives of neurology 1998
D Kidd J Nelson F Jones H Dusoir I Wallace S McKinstry V Patterson

W e describe a 16-year-old boy with juvenile metachromatic leukodystrophy who was treated with bone marrow transplantation. Follow-up over 8 years showed no increase in symptoms, no progression of neurological signs, and no neuropsychological deterioration. We conclude that bone marrow transplantation may increase brain levels of arylsulfatase A enough to prevent deterioration in patients with ...

Journal: :American journal of ophthalmology 1980
J J Weiter M Feingold E H Kolodny S S Raghaven

A family exhibiting a leukocytic arylsulfatase A deficiency, probably inherited in an autosomal recessive manner, differed from patients with typical metachromatic leukodystrophy in that sulfatiduria was absent and there was readily detectable cerebroside sulfatase activity. To our knowledge, this family was unique in that there were no known members with metachromatic leukodystrophy and the on...

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