Hereditary neuropathy with liability to pressure palsies: A case report

Clinical Orthopaedics and Related Research

Volumn 385, Issue , 2001, Pages 253-255

  Jafarnia, Kourosh ^a   Sullivan, Michael J ^a   Hildreth, David H ^a,b  

^a HOUSTON METHODIST HOSPITAL   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 17P; CHROMOSOME DELETION; DEMYELINATION; FEMALE; HEREDITARY NEUROPATHY; HUMAN; MUSCLE WEAKNESS; NEUROPATHY; PARALYSIS; PARESTHESIA; PRIORITY JOURNAL;

EID: 0035082937     PISSN: 0009921X     EISSN: 15281132     Source Type: Journal    
DOI: 10.1097/00003086-200104000-00036     Document Type: Article

References (10)

1. Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies
2. DNA deletion associated with hereditary neuropathy with liability to pressure palsies
3. Molecular cytogenetics of contiguous gene syndromes: Mechanisms and consequences of gene dosage imbalance
4. 17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1
5. Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients
6. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease Type 1 and hereditary neuropathy with liability to pressure palsies: A European collaborative study
7. A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies
8. Deletions of chromosomes 17p11.2 in multifocal neuropathies
9. Hereditary neuropathy with liability to pressure palsies: A clinical, electrophysiological and morphologic study