Hereditary motor and sensor neuropathy: A cause of acute stridor

Emergency Medicine Journal

Volumn 22, Issue 9, 2005, Pages 666-667

  Jaiganesh, T ^a   Bentley, A M ^a,b  

^a NORTH MANCHESTER GENERAL HOSPITAL   (United Kingdom)

^b WYTHENSHAWE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE DISEASE; ADULT; AIRWAY OBSTRUCTION; AREFLEXIA; ASTHMA; CASE REPORT; COUGHING; DEMYELINATING NEUROPATHY; DYSPNEA; EMERGENCY WARD; ENDOTRACHEAL INTUBATION; FAMILY HISTORY; FEMALE; FLU LIKE SYNDROME; HEREDITARY MOTOR SENSORY NEUROPATHY; HOSPITAL DISCHARGE; HUMAN; INTENSIVE CARE UNIT; LARYNGOSCOPY; LARYNX EDEMA; MUSCLE ATROPHY; NEUROLOGIC EXAMINATION; PRIORITY JOURNAL; REVIEW; STRIDOR; TRACHEOSTOMY; VOCAL CORD PARALYSIS;

ACUTE DISEASE; CHARCOT-MARIE-TOOTH DISEASE; FEMALE; HUMANS; MIDDLE AGED; RESPIRATORY SOUNDS; VOCAL CORD PARALYSIS;

EID: 23944520396     PISSN: 14720205     EISSN: None     Source Type: Journal    
DOI: 10.1136/emj.2003.009886     Document Type: Review

References (4)

1. Charcot JM, Marie P. On a specific form of frequently familial progressive muscular atrophy beginning in the feet and legs and later affecting the hands (in French). Rev Med 1886; 6:97-138.
2. Tooth H. The peroneal type of progressive muscular atrophy. London: Lewis HK Publishers, 1886.
3. Sulcia L, Blitzer A, Lovelace RE, et al. Vocal fold paresis of charcot-marie-tooth disease. Ann Otol Rhinol Laryngol 2001;110:1072-76.
4. Dyck PJ, Litchy WJ, Minnerath S, et al. Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis. Ann Neurol 1994;35:608-15.