central core myopathy: An inherited congenital myopathic condition characterized by weakness and hypotonia in infancy and delayed motor development. Muscle biopsy reveals a condensation of myofibrils and myofibrillar material in the central portion of each muscle fiber. (Adams et al., Principles of Neurology, 6th ed, p1452)
| Name | G6_CONMYOP |
|---|---|
| Long name | Congenital myopathies |
| Hospital Discharge registry | ICD-10: G712, ICD-9: 3590A |
| Cause of Death registry | ICD-10: G712, ICD-9: 3590A |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
| Latin name | Myopathiae congenitae |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 25 | 15 | 10 |
| Unadjusted prevalence (%) | 0.01 | 0.01 | 0.01 |
| Mean age at first event (years) | 38.43 | 35.56 | 42.74 |
| Case fatality at 5-years (%) | 12.00 | 13.33 | 10.00 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 2.0 | 1.0 | 2.0 |
| Recurrence at 6 months (%) | 36.00 | 40.00 | 30.00 |
before Congenital myopathies
after Congenital myopathies
Loading survival analyses plot…
Loading survival analyses table…