by Gregor Kuhlenbäumer
Hereditary Peripheral Neuropathies deals with the Charcot-Marie-Tooth group and related primary hereditary neuropathies and integrates the clinical features with the current knowledge about the molecular genetics and biology of these diseases.
Contents
General Part
- Architecture of the Peripheral Nerve
Approach to the Patient with Suspected Hereditary Neuropathy
- Clinical Evaluation and Differential Diagnosis
- Electrodiagnosis Evaluation of Hereditary Polyneuropathies
- Principles of Pathology and Nerve Biopsy
Specific Neuropathies, Treatment and Counseling
- Overview of the Classification and Genetics of Hereditary Peripheral Neuropathies and Rare Unclassified Forms
- Charcot-Marie-Tooth Disease Type 1 (CMT1) and Hereditary Neuropathy with Liability to Pressure Palsy (HNPP)
- CMT2, Dominant Intermediate CMT and CMTX
- Distal Hereditary Motor Neuropathies (dHMN)
- Hereditary Sensory and Autonomic Neuropathies (HSAN)
- Hereditary Neuralgic Amyotrophy (HNA)
- Molecular Genetic Diagnosis of Hereditary Neuropathies
- Genetic Counseling
- Medical Treatment of Hereditary Neuropathies
- Orthopedic Aspects in Diagnosis, Clinical Management and Therapy of CMT Patients
- Animal Models of Hereditary Neuropathies
Index