A rare genetic disorder in the differential diagnosis of the entrapment neuropathies: Hereditary neuropathy with liability to pressure palsies

Journal of Clinical Rheumatology

Volumn 12, Issue 2, 2006, Pages 78-82

  Koc, Filiz ^a,b   Güzel, Rengin ^a   Benliday, Ilke Coskun ^a   Yerdelen, Deniz ^a   Güzel, Irfan ^a   Sarca, Yakup ^a  

^a CUKUROVA UNIVERSITY   (Turkey)

^b NONE   (Turkey)

Author keywords

Clinical; Electrophysiological findings; Genetic; Hereditary neuropathy with liability to pressure palsies (HNPP)

Indexed keywords

ADULT; ANAMNESIS; ARTICLE; CARPAL TUNNEL SYNDROME; CHROMOSOME DELETION; CLINICAL ARTICLE; DIFFERENTIAL DIAGNOSIS; ELECTROPHYSIOLOGY; FEMALE; FINGER; GENE DELETION; GENETIC DISORDER; HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY; HISTOPATHOLOGY; HUMAN; MALE; MUSCLE ATROPHY; MUSCLE WEAKNESS; MUSCULOSKELETAL DISEASE; NERVE COMPRESSION; NEUROLOGIC EXAMINATION; NEUROMUSCULAR DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PARESTHESIA; PHYSICAL EXAMINATION; PHYSICIAN; POINT MUTATION; PRIORITY JOURNAL;

ADULT; DIAGNOSIS, DIFFERENTIAL; FEMALE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MALE; MIDDLE AGED; NEURAL CONDUCTION; NEUROLOGIC EXAMINATION; PEDIGREE;

EID: 33748167813     PISSN: 10761608     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.rhu.0000208634.26253.17     Document Type: Article

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