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Literature DB >> 3420560

Diaphragm weakness in Charcot-Marie-Tooth disease.

C M Laroche¹, N Carroll, J Moxham, N N Stanley, R J Evans, M Green.
1. Brompton Hospital, London.

Abstract

Two patients are described with Charcot-Marie-Tooth disease and chronic peripheral neuropathy. Both had dyspnoea, orthopnoea, and evidence of severe diaphragm weakness. Expiratory muscle function was well preserved and abnormalities of gas exchange during sleep were only minor.

Entities: Disease Species

Mesh：

Year: 1988 PMID： 3420560 PMCID： PMC461315 DOI： 10.1136/thx.43.6.478

Source DB: PubMed Journal: Thorax ISSN： 0040-6376 Impact factor: 9.139

7 in total

1. Alveolar gas tensions, pulmonary ventilation and blood pH during physiologic sleep in normal subjects.

Authors: E D ROBIN; R D WHALEY; C H CRUMP; D M TRAVIS
Journal: J Clin Invest Date: 1958-07 Impact factor: 14.808

2. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.

Authors: P J Dyck; E H Lambert
Journal: Arch Neurol Date: 1968-06

3. Assessment of diaphragm weakness.

Authors: A Mier-Jedrzejowicz; C Brophy; J Moxham; M Green
Journal: Am Rev Respir Dis Date: 1988-04

4. Predicted normal values for maximal respiratory pressures in caucasian adults and children.

Authors: S H Wilson; N T Cooke; R H Edwards; S G Spiro
Journal: Thorax Date: 1984-07 Impact factor: 9.139

5. Phrenic nerve stimulation in normal subjects and in patients with diaphragmatic weakness.

Authors: A Mier; C Brophy; J Moxham; M Green
Journal: Thorax Date: 1987-11 Impact factor: 9.139

6. Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease).

Authors: C K Chan; V Mohsenin; J Loke; J Virgulto; M L Sipski; R Ferranti
Journal: Chest Date: 1987-04 Impact factor: 9.410

7. Diaphragm function and alveolar hypoventilation.

Authors: J Davis; M Goldman; L Loh; M Casson
Journal: Q J Med Date: 1976-01

7 in total

8 in total

Diaphragm weakness in Charcot-Marie-Tooth disease.

1. Alveolar gas tensions, pulmonary ventilation and blood pH during physiologic sleep in normal subjects.

2. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.

3. Assessment of diaphragm weakness.

4. Predicted normal values for maximal respiratory pressures in caucasian adults and children.

5. Phrenic nerve stimulation in normal subjects and in patients with diaphragmatic weakness.

6. Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease).

7. Diaphragm function and alveolar hypoventilation.

Review 1. Diaphragmatic paresis: pathophysiology, clinical features, and investigation.

2. Diaphragmatic weakness in hereditary motor and sensory neuropathy.

3. Anaesthesia for Charcot-Marie-Tooth disease: a review of 86 cases.

4. Charcot-marie-tooth disease as a disabling disorder.

5. Respiratory dysfunction in Charcot-Marie-Tooth disease type 1A.

6. Neuromuscular disease, respiratory failure and cor pulmonale.

7. Oral health, temporomandibular disorder, and masticatory performance in patients with Charcot-Marie-Tooth type 2.

8. Multiple respiratory complications in a patient with Charcot-Marie-Tooth disease with MFN2 mutation.