Hereditary neuropathy with liability to pressure palsies: case report and discussion
- PMID: 18751796
- PMCID: PMC2504259
- DOI: 10.1007/s11420-007-9056-1
Hereditary neuropathy with liability to pressure palsies: case report and discussion
Abstract
Hereditary neuropathy with liability to pressure palsies (HNPP) is an uncommon diagnosis that should be considered in patients with multiple compressive neuropathies. We present the case of a woman who presented with bilateral hand numbness and weakness. Electrodiagnostic testing revealed bilateral carpal tunnel syndrome, bilateral ulnar neuropathy at the elbow, left peroneal neuropathy at the fibular head, and a primarily demyelinating generalized sensorimotor neuropathy. Subsequent genetic testing identified a deletion at chromosome 17p11.2 to confirm the diagnosis of HNPP. Treatment of this largely self-limiting disease is controversial, and this patient suffered minimal disability with treatment including splinting and surgical releases.
Figures


Similar articles
-
Unusual presentation of hereditary neuropathy with liability to pressure palsies.J Brachial Plex Peripher Nerve Inj. 2008 Jan 24;3:2. doi: 10.1186/1749-7221-3-2. J Brachial Plex Peripher Nerve Inj. 2008. PMID: 18218131 Free PMC article.
-
Overview of hereditary neuropathy with liability to pressure palsies.Ann N Y Acad Sci. 1999 Sep 14;883:14-21. Ann N Y Acad Sci. 1999. PMID: 10586225 Review.
-
Heterogeneous Presentation of Hereditary Neuropathy With Liability to Pressure Palsies: Clinical and Electrodiagnostic Findings in Three Patients.Cureus. 2022 Dec 7;14(12):e32296. doi: 10.7759/cureus.32296. eCollection 2022 Dec. Cureus. 2022. PMID: 36628033 Free PMC article.
-
Overview of Hereditary Neuropathy with Liability to Pressure Palsies.Ann N Y Acad Sci. 1999 Oct;883(1):14-21. doi: 10.1111/j.1749-6632.1999.tb08562.x. Ann N Y Acad Sci. 1999. PMID: 29086948
-
Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.Neuromolecular Med. 2006;8(1-2):159-74. doi: 10.1385/NMM:8:1:159. Neuromolecular Med. 2006. PMID: 16775374 Review.
Cited by
-
New evidence for secondary axonal degeneration in demyelinating neuropathies.Neurosci Lett. 2021 Jan 23;744:135595. doi: 10.1016/j.neulet.2020.135595. Epub 2020 Dec 24. Neurosci Lett. 2021. PMID: 33359733 Free PMC article. Review.
-
DTI Study of Cerebral Normal-Appearing White Matter in Hereditary Neuropathy With Liability to Pressure Palsies (HNPP).Medicine (Baltimore). 2015 Oct;94(43):e1909. doi: 10.1097/MD.0000000000001909. Medicine (Baltimore). 2015. PMID: 26512614 Free PMC article.
-
Anesthetic Considerations for Patients with Hereditary Neuropathy with Liability to Pressure Palsies: A Narrative Review.Healthcare (Basel). 2024 Apr 19;12(8):858. doi: 10.3390/healthcare12080858. Healthcare (Basel). 2024. PMID: 38667620 Free PMC article. Review.
-
Rapid genetic screening of Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies patients.Neural Regen Res. 2012 Nov 15;7(32):2522-7. doi: 10.3969/j.issn.1673-5374.2012.32.006. Neural Regen Res. 2012. PMID: 25337104 Free PMC article.
-
Literature review of clinical analysis of hereditary neuropathy with liability to pressure palsies.J Neurol. 2024 Dec 12;272(1):41. doi: 10.1007/s00415-024-12839-7. J Neurol. 2024. PMID: 39666198 Free PMC article. Review.
References
-
- {'text': '', 'ref_index': 1, 'ids': [{'type': 'PubMed', 'value': '12682341', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/12682341/'}]}
- Koehler PJ (2003) Hereditary neuropathy with liability to pressure palsies: the first publication (1947). Neurology 60(7):1211–1213 - PubMed
-
- {'text': '', 'ref_index': 1, 'ids': [{'type': 'DOI', 'value': '10.1016/S0960-8966(97)00100-4', 'is_inner': False, 'url': 'https://doi.org/10.1016/s0960-8966(97)00100-4'}, {'type': 'PubMed', 'value': '9447611', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/9447611/'}]}
- Mertogja P, Silander K, Kalimo H et al (1997) Epidemiology of hereditary neuropathy with liability to pressure palsies in south western Finland. Neuromuscul Disord 7(8):529–532 - PubMed
-
- {'text': '', 'ref_index': 1, 'ids': [{'type': 'DOI', 'value': '10.1097/01.rhu.0000208634.26253.17', 'is_inner': False, 'url': 'https://doi.org/10.1097/01.rhu.0000208634.26253.17'}, {'type': 'PubMed', 'value': '16601541', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/16601541/'}]}
- Koc F, Guzel R, Benliday IC et al (2006) A rare genetic disorder in the differential diagnosis of the entrapment neuropathies: hereditary neuropathy with liability to pressure palsies. J Clin Rheumatol 12(2):78–82 - PubMed
-
- {'text': '', 'ref_index': 1, 'ids': [{'type': 'PubMed', 'value': '10227632', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/10227632/'}]}
- Mouton P, Tardieu S, Gouider R et al (1999) Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion. Neurology 52(7):1440–1446 - PubMed
-
- {'text': '', 'ref_index': 1, 'ids': [{'type': 'DOI', 'value': '10.1016/S0960-8966(99)00103-0', 'is_inner': False, 'url': 'https://doi.org/10.1016/s0960-8966(99)00103-0'}, {'type': 'PubMed', 'value': '10734269', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/10734269/'}]}
- Dubourg O, Mouton P, Brice A, et al (2000) Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies. Neuromuscul Disord 10:206–208 - PubMed
LinkOut - more resources
Full Text Sources