지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2017.1
- 수록면
- 71 - 75 (5page)
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초록· 키워드
오류제보하기
Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant disorder characterized by recurrent entrapment neuropathies following an episode of compression or trauma. Reports on bilateral brachial plexopathy of HNPP are rare. We report on a case of a 21-year-old female patient with no past medical history, who presented with sudden paralysis and hypoesthesia of bilateral upper extremities after undergoing liposuction. Clinical and electrodiagnostic tests were consistent with brachial plexopathy. Genetic study for the peripheral myelin protein-22 (PMP22) gene confirmed the diagnosis of HNPP presenting with bilateral brachial plexopathy. This case indicates that HNPP should be suspected in patients with brachial plexopathy when it develops after pressure-leading events such as a minor surgical procedure.
목차
등록된 정보가 없습니다.
참고문헌 (10)
참고문헌 신청
Bulusu S / 2011 / A report of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy: The value of complete electrodiagnostic testi
Infante J / 2001 / Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion / Muscle Nerve 24 : 1149 ~ 1155
Kim KE / 2014 / Characteristic features of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy in soldiers / J Neurol Sci 346 :
Li J / 2013 / The PMP22 gene and its related diseases / Mol Neurobiol 47 : 673 ~ 698
Mouton P / 1999 / Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion / Neurology 52 : 1440 ~ 1446
Infante J / 2001 / Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion / Muscle Nerve 24 : 1149 ~ 1155
Kim KE / 2014 / Characteristic features of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy in soldiers / J Neurol Sci 346 :
Li J / 2013 / The PMP22 gene and its related diseases / Mol Neurobiol 47 : 673 ~ 698
Mouton P / 1999 / Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion / Neurology 52 : 1440 ~ 1446
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