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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1997 Nov;34(11):889–892. doi: 10.1136/jmg.34.11.889

Atypical hereditary neuropathy with liability to pressure palsies (HNPP): the value of direct DNA diagnosis.

M Sessa 1, R Nemni 1, A Quattrini 1, U Del Carro 1, L Wrabetz 1, N Canal 1
PMCID: PMC1051114  PMID: 9391880

Abstract

We report two patients with suspected hereditary liability to pressure palsies. Neurophysiological studies showed a mixed axonal-demyelinating sensory-motor polyneuropathy with focal slowing of conduction velocities at the common sites of entrapment. Morphological studies on sural nerve biopsy from the proband showed active axonal regeneration without typical tomacula. Molecular analysis confirmed the presence of a deletion of chromosome 17p11.2 in both patients. Our observation confirms the heterogeneity of hereditary liability to pressure palsies and the relevance of DNA testing for the diagnosis of this hereditary neuropathy.

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