Version May 2024
| Disorder | Inheritance | Chromosome (gene) | Clinical features |
| Hereditary neuropathy with pressure palsy | AD | 17p11.2-12 (PMP22) | Usual onset in second decade Isolated nerve palsies after trivial trauma Palsies resolve in days to months Cranial nerve involvement Nerve deafness Scoliosis |
| Hereditary brachial plexopathy | AD | 17q25 (SEPT9) | Onset in childhood Pain followed by paresis of brachial plexus muscles Resolves spontaneously and recurs at irregular intervals Winging of the scapula Facial weakness Autonomic nervous system dysfunction Short stature Hypertelorism Small palpebral fissures Small face |
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