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Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu

Year 2006, Volume: 23 Issue: 1, 33 - 38, 30.12.2009

Abstract

Hereditary neuropathy with liability to pressure palsy (HNPP) is a rare autosomal dominant disorder characterized by mononeuropathies at sites subject to compression. It causes recurrent, painless and transitory acute nerve palcies and rarely presents in two extremities. In this report, we describe a case of HNPP presenting as isolated, bilateral, acute, painless ulnar palsy. Neurologic examination revealed atrophy and weakness limited in intrinsic hand muscles bilaterally. Electrophysiological examination exhibited mild sensorimotor p o lyn e uro p a thy, bilateral conduction block of the ulnar nerve at the elbow and mild partial acute denervation findings on the abductor digiti minimi and first dorsal interosseus muscles. The diagnosis was based on clinical and electrophysiological features. This case is reported to emphasize the importance of exploring subclinic polyneuropathy in the patients who admit with multiple, acute, painless neuropathies and the value of electrophysiological examination in the diagnosis of HNPP.


Basınca hassas herediter nöropati (BHHN) basıya maruz kalan bölgelerde mononöropatiler-le karakterize nadir görülen otozomal dominant geçiş gösteren bir hastalıktır. Ağrısız, tekrar-layıcı ve geçici akut sinir parezilerine neden olur ve nadiren iki ekstremitede meydana gelir. Biz; izole, bilateral, akut, ağrısız ulnar parezi ile ortaya çıkan bir BHHN vakası sunduk. Nörolojik muayenesinde bilateral tenar kaslar hariç olmak üzere, intrensek el kaslarında sınırlı atrofi ve güçsüzlük tespit edildi. Elektrofizyolojik incelemede hafif bir sensorimotor polinö-ropati, dirsekte iki yanlı ulnar sinirin tam ileti bloğu ile abduktor digiti minimi ve birinci dorsal interosseus kaslarında hafif parsiyel akut denervasyon bulguları mevcuttu. Tanı elektro-fizyolojik ve klinik özelliklere dayanılarak konuldu. Bu olgu birden fazla sayıda, akut, ağrısız nöropatilerle başvuran hastalarda subklinik polinöropati varlığını göstermenin önemini ve BHHN tanısında elektrofizyolojik incelemenin değerini vurgulamak için sunulmuştur.

References

  • Orstavik K, Skard Heier M, Young P, Stogbauer F. Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies. Muscle Nerve. 2001;24: 1093–1096.
  • Kaneko S, Ito H, Kusaka H, Imai T, Nishimura T, Yoshikawa H. Peripheral myelin protein-22 gene deletion in two unrelated Japanese pedigrees with hereditary neuropathy with liability to pressure palsies. Muscle Nerve. 1996;19: 675–676.
  • Shaibani A, Gooch C, Harati Y. Moving toes and myoclonus associated with hereditary neuropathy with liability to pressure palsy (HNPP). Muscle Nerve. 1997;20: 881–883.
  • Pareyson D, Solari A, Taroni F, Botti S, Fallica E, Scaioli V, Ciano C, Sghirlanzoni A. Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy. Muscle Nerve. 1998;21: 1686–1691.
  • Li J, Krajewski K, Shy ME, Lewis RA. Hereditary n e u r o p a t h y with liability to pressure palsy: the e l e ctrophysiology fits the name. Neurology. 2002; 25: 1769–1773.
  • Goikhman I, Meer J, Zelnik N. Hereditary neuropathy with liability to pressure palsies in infancy. Pediatr Neurol. 2003; 28: 307–309.
  • Infante J, Garcia A, Combarros O, Mateo JI, Berciano, J, Sedano MJ, Gutierrez-Rivas EJ, Palau F. Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion. Muscle Nerve. 2001; 24: 1149–1155.
  • Amato AA, Dumitru D. Hereditary Neuropathies. Dumitru D, Amato AA, Zwarts MJ. Electrodiagnostic Medicine. Philadelphia: Hanley & Belfus, Inc. 2002. second edition; 899–936.
  • Crum, BA, Sorenson EJ, Abad GA, Dyck PJ. Fulminant case of hereditary neuropathy with l i a b i l i t y to pressure palsy. Muscle Nerve. 2000; 23: 979–983.
  • Horowitz SH, Spollen LE, Yu W. Hereditary neuropathy with liability to pressure palsy: fulminant development with axonal loss during military t r a i n i n g . J Neurol Neurosurg Psychiatry. 2004; 75: 1629–1631.
  • Uncini A, Di Guglielmo G, Di Muzio A, Gambi D, Sabatelli M, Mignogna T, Tonali P, Marzella R, Finelli P, Archidiacono N, et al. Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication. Muscle Nerve. 1995; 18: 628–635.
  • Gonnaud PM, Sturtz F, Fourbil Y, Bonnebouche C, Tranchant C, Warter JM, sChazot G, Bady B, Vial C, Brechard AS, et al. DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations. Acta Neurol Scand. 1995; 92: 313–318.
Year 2006, Volume: 23 Issue: 1, 33 - 38, 30.12.2009

Abstract

References

  • Orstavik K, Skard Heier M, Young P, Stogbauer F. Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies. Muscle Nerve. 2001;24: 1093–1096.
  • Kaneko S, Ito H, Kusaka H, Imai T, Nishimura T, Yoshikawa H. Peripheral myelin protein-22 gene deletion in two unrelated Japanese pedigrees with hereditary neuropathy with liability to pressure palsies. Muscle Nerve. 1996;19: 675–676.
  • Shaibani A, Gooch C, Harati Y. Moving toes and myoclonus associated with hereditary neuropathy with liability to pressure palsy (HNPP). Muscle Nerve. 1997;20: 881–883.
  • Pareyson D, Solari A, Taroni F, Botti S, Fallica E, Scaioli V, Ciano C, Sghirlanzoni A. Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy. Muscle Nerve. 1998;21: 1686–1691.
  • Li J, Krajewski K, Shy ME, Lewis RA. Hereditary n e u r o p a t h y with liability to pressure palsy: the e l e ctrophysiology fits the name. Neurology. 2002; 25: 1769–1773.
  • Goikhman I, Meer J, Zelnik N. Hereditary neuropathy with liability to pressure palsies in infancy. Pediatr Neurol. 2003; 28: 307–309.
  • Infante J, Garcia A, Combarros O, Mateo JI, Berciano, J, Sedano MJ, Gutierrez-Rivas EJ, Palau F. Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion. Muscle Nerve. 2001; 24: 1149–1155.
  • Amato AA, Dumitru D. Hereditary Neuropathies. Dumitru D, Amato AA, Zwarts MJ. Electrodiagnostic Medicine. Philadelphia: Hanley & Belfus, Inc. 2002. second edition; 899–936.
  • Crum, BA, Sorenson EJ, Abad GA, Dyck PJ. Fulminant case of hereditary neuropathy with l i a b i l i t y to pressure palsy. Muscle Nerve. 2000; 23: 979–983.
  • Horowitz SH, Spollen LE, Yu W. Hereditary neuropathy with liability to pressure palsy: fulminant development with axonal loss during military t r a i n i n g . J Neurol Neurosurg Psychiatry. 2004; 75: 1629–1631.
  • Uncini A, Di Guglielmo G, Di Muzio A, Gambi D, Sabatelli M, Mignogna T, Tonali P, Marzella R, Finelli P, Archidiacono N, et al. Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication. Muscle Nerve. 1995; 18: 628–635.
  • Gonnaud PM, Sturtz F, Fourbil Y, Bonnebouche C, Tranchant C, Warter JM, sChazot G, Bady B, Vial C, Brechard AS, et al. DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations. Acta Neurol Scand. 1995; 92: 313–318.
There are 12 citations in total.

Details

Primary Language English
Journal Section Basic Medical Sciences
Authors

A.OYTUN Bayrak This is me

H. Erdem Tilki This is me

Publication Date December 30, 2009
Submission Date October 26, 2009
Published in Issue Year 2006 Volume: 23 Issue: 1

Cite

APA Bayrak, A., & Erdem Tilki, H. (2009). Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu. Journal of Experimental and Clinical Medicine, 23(1), 33-38. https://doi.org/10.5835/jecm.v23i1.56
AMA Bayrak A, Erdem Tilki H. Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu. J. Exp. Clin. Med. December 2009;23(1):33-38. doi:10.5835/jecm.v23i1.56
Chicago Bayrak, A.OYTUN, and H. Erdem Tilki. “Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu”. Journal of Experimental and Clinical Medicine 23, no. 1 (December 2009): 33-38. https://doi.org/10.5835/jecm.v23i1.56.
EndNote Bayrak A, Erdem Tilki H (December 1, 2009) Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu. Journal of Experimental and Clinical Medicine 23 1 33–38.
IEEE A. Bayrak and H. Erdem Tilki, “Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu”, J. Exp. Clin. Med., vol. 23, no. 1, pp. 33–38, 2009, doi: 10.5835/jecm.v23i1.56.
ISNAD Bayrak, A.OYTUN - Erdem Tilki, H. “Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu”. Journal of Experimental and Clinical Medicine 23/1 (December 2009), 33-38. https://doi.org/10.5835/jecm.v23i1.56.
JAMA Bayrak A, Erdem Tilki H. Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu. J. Exp. Clin. Med. 2009;23:33–38.
MLA Bayrak, A.OYTUN and H. Erdem Tilki. “Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu”. Journal of Experimental and Clinical Medicine, vol. 23, no. 1, 2009, pp. 33-38, doi:10.5835/jecm.v23i1.56.
Vancouver Bayrak A, Erdem Tilki H. Bilateral Ulnar Palsi İle Ortaya Çıkan Basınca Hassas Herediter Nöropati Olgusu. J. Exp. Clin. Med. 2009;23(1):33-8.