Hereditary neuropathy with liability to pressure palsies in children

Pediatric Neurology

Volumn 21, Issue 5, 1999, Pages 818-821

  Felice, Kevin J ^a,c   Leicher, Carol R ^b,c   Dimario Jr, Francis J ^b,c  

^a UNIVERSITY OF CONNECTICUT SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CONNECTICUT   (United States)

^c Div Pediat Neurol Connecticut C   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; DEMYELINATING NEUROPATHY; DNA DETERMINATION; FEMALE; GENE DELETION; HUMAN; MALE; MUSCLE ATROPHY; MUSCLE WEAKNESS; NERVE CONDUCTION; NEUROPATHY; PRIORITY JOURNAL; SHOULDER;

EID: 0032696811     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(99)00086-7     Document Type: Article

References (12)

1. Chance P.F., Pleasure D. Charcot-Marie-Tooth syndrome. Arch Neurol. 50:1993;1180-1184.
2. Nelis E., Haites N., Van Broeckhoven C. Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies. Hum Mutat. 13:1999;11-28.
3. Stewart JD. The nerves arising from the brachial plexus. In: Focal peripheral neuropathies, 2nd ed. New York: Raven Press, 1993:150-2.
4. Felice K.J., Poole R.M., Blaivas M., Albers J.W. Hereditary neuropathy with liability to pressure palsies masquerading as slowly progressive polyneuropathy. Eur Neurol. 34:1994;173-176.
5. Gabreëls-Festen A.A.W.M., Gabreëls F.J.M., Joosten E.M.G., Vingerhoets H.M., Renier W.O. Hereditary neuropathy with liability to pressure palsies in childhood. Neuropediatrics. 23:1992;138-143.
6. Cruz-Martinez A., Arpa J. Carpal tunnel disease in childhood Study of 6 cases . Electroencephalogr Clin Neurophysiol. 109:1998;304-308.
7. Van Wensen P.J.M. Hereditary neuropathy with liability to pressure palsies. Vinken P.J., Bruyn G.W., Klawans H.L., Vianney DeJong J.M.B. Handbook of clinical neurology. 1991;61-70 Elsevier Science, Amsterdam.
8. Felice K.J. Acute anterior interosseous neuropathy in a patient with hereditary neuropathy with liability to pressure palsies a clinical and electromyographic study . Muscle Nerve. 18:1995;1329-1331.
9. Pareyson D., Solari A., Taroni F., et al. Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy. Muscle Nerve. 21:1998;1686-1691.
10. Cruz-Martinez A., Bort S., Arpa J., Duarte J., Palau F. Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2. Eur J Neurol. 4:1997;274-286.
11. Jones H.J. Mononeuropathies. Pediatric clinical electromyography. 1996;171-250 Lippincott-Raven, Philadelphia.
12. Pellegrino J.E., Rebbeck T.R., Brown M.J., Bird T.D., Chance P.F. Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17q. Neurology. 46:1996;1128-1132.