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Your search keyword '"J. Meuleman"' showing total 3 results
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3 results on '"J. Meuleman"'

1. [Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis]

Author

F, Stögbauer, P, Young, G, Kuhlenbäumer, J, Meuleman, V, Timmerman, C, van Broeckhoven, G, Kurlemann, and E B, Ringelstein

Subjects
Electrophysiology, Genotype, Brachial Plexus Neuritis, Humans, Family, Amyloid Neuropathies, Molecular Biology, Chromosomes, Human, Pair 17, Pedigree
Abstract

Hereditary neuralgic amyotrophy (HNA) and hereditary neuropathy with liability to pressure palsies (HNPP) are hereditary focal neuropathies. In this study we describe three families suffering from HNA. These families were examined clinically and electrophysiologically. Linkage analysis with markers from distal chromosome 17 was performed in a three-generation family. HNA could be separated from HNPP in all three families based on clinical and electrophysiological findings. HNA was characterised by recurrent episodes of painful brachial plexus lesions. In contrast to HNPP, no evidence for generalised neuropathy was found in the HNA families. Linkage analysis confirmed the HNA locus on distal chromosome 17. Additionally, we were able to refine the HNA locus to a 16 cM region on chromosome 17q24-q25.

Published
1998

2. Hereditäre neuralgische Amyotrophie (HNA): klinische und molekulargenetische Befunde

Author

Vincent Timmerman, Gerd Kurlemann, Gregor Kuhlenbäumer, C. Van Broeckhoven, Peter Young, Erich Bernd Ringelstein, Florian Stögbauer, and J. Meuleman

Subjects
Pathology, medicine.medical_specialty, Brachial plexus lesions, business.industry, Locus (genetics), Hereditary neuralgic amyotrophy, medicine.disease, Chromosome 17 (human), Psychiatry and Mental health, Neurology, Genetic linkage, medicine, Neurology (clinical), business
Abstract

Hereditary neuralgic amyotrophy (HNA) and hereditary neuropathy with liability to pressure palsies (HNPP) are hereditary focal neuropathies. In this study we describe three families suffering from HNA. These families were examined clinically and electrophysiologically. Linkage analysis with markers from distal chromosome 17 was performed in a three-generation family. HNA could be separated from HNPP in all three families based on clinical and electrophysiological findings. HNA was characterised by recurrent episodes of painful brachial plexus lesions. In contrast to HNPP, no evidence for generalised neuropathy was found in the HNA families. Linkage analysis confirmed the HNA locus on distal chromosome 17. Additionally, we were able to refine the HNA locus to a 16 cM region on chromosome 17q24-q25.

Published
1998

3. [Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis].

Author

Stögbauer F, Young P, Kuhlenbäumer G, Meuleman J, Timmerman V, van Broeckhoven C, Kurlemann G, and Ringelstein EB

Subjects
Amyloid Neuropathies physiopathology, Amyloid Neuropathies psychology, Brachial Plexus Neuritis physiopathology, Chromosomes, Human, Pair 17, Electrophysiology, Family, Genotype, Humans, Molecular Biology, Pedigree, Amyloid Neuropathies genetics, Brachial Plexus Neuritis genetics
Abstract

Hereditary neuralgic amyotrophy (HNA) and hereditary neuropathy with liability to pressure palsies (HNPP) are hereditary focal neuropathies. In this study we describe three families suffering from HNA. These families were examined clinically and electrophysiologically. Linkage analysis with markers from distal chromosome 17 was performed in a three-generation family. HNA could be separated from HNPP in all three families based on clinical and electrophysiological findings. HNA was characterised by recurrent episodes of painful brachial plexus lesions. In contrast to HNPP, no evidence for generalised neuropathy was found in the HNA families. Linkage analysis confirmed the HNA locus on distal chromosome 17. Additionally, we were able to refine the HNA locus to a 16 cM region on chromosome 17q24-q25.

Published
1998
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