Hereditary neuropathy with liability to pressure palsies in childhood: Case series and literature update

Neuromuscular Disorders

Volumn 25, Issue 9, 2015, Pages 693-698

  Chrestian, Nicolas ^a   McMillan, Hugh ^b   Poulin, Chantal ^c   Campbell, Craig ^d   Vajsar, Jiri ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^c MONTREAL CHILDREN S HOSPITAL   (Canada)

^d CHILDREN S HEALTH RESEARCH INSTITUTE   (Canada)

Author keywords

Childhood; Hereditary; HNPP; Mononeuropathies; PMP22 protein

Indexed keywords

ACROPARESTHESIA; ACUTE DISEASE; ADOLESCENT; ARTICLE; BRACHIAL PLEXUS PALSY; CARPAL TUNNEL SYNDROME; CASE STUDY; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; CONVALESCENCE; DEMYELINATION; ELECTROMYOGRAPHY; ELECTROPHYSIOLOGY; FAMILY HISTORY; FEMALE; FOLLOW UP; FOOT MALFORMATION; GENE; GENE DELETION; GENERALIZED DEMYELINATING SENSORY-MOTOR POLYNEUROPATHY; GENETIC SCREENING; HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY; HEREDITY; HUMAN; LIMB WEAKNESS; MALE; MEDIAN NERVE ENTRAPMENT; MONONEUROPATHY; NERVE COMPRESSION; NERVE CONDUCTION; NEUROPATHY; PARALYSIS; PARESTHESIA; PERONEUS NERVE PARALYSIS; PES CAVUS; PMP22 GENE; POLYNEUROPATHY; PRESCHOOL CHILD; PRIORITY JOURNAL; RARE DISEASE; RUCKSACK SYNDROME; SCHOOL CHILD; ARTHROGRYPOSIS; CASE REPORT; GENETICS; HEREDITARY SENSORY AND MOTOR NEUROPATHY; PATHOPHYSIOLOGY;

MYELIN PROTEIN; PMP22 PROTEIN, HUMAN;

ADOLESCENT; ARTHROGRYPOSIS; CHILD; CHILD, PRESCHOOL; FEMALE; GENE DELETION; HEREDITARY SENSORY AND MOTOR NEUROPATHY; HUMANS; MALE; MYELIN PROTEINS; NEURAL CONDUCTION;

EID: 84939505018     PISSN: 09608966     EISSN: 18732364     Source Type: Journal    
DOI: 10.1016/j.nmd.2015.06.463     Document Type: Article

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