Congenital and developmental myasthenia

Myasthenia gravis: Myasthenia gravis (MG) is a rare, clinically heterogeneous, autoimmune disorder of the neuromuscular junction characterized by fatigable weakness of voluntary muscles.

Endpoint definition

Name G6_CONDEVMYA
Long name Congenital and developmental myasthenia
Hospital Discharge registry ICD-10: G702
Cause of Death registry ICD-10: G702
Level in the ICD-hierarchy 3
First defined in version DF2

Summary Statistics

Key figures

All Female Male
Number of individuals 14 8 6
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 56.51 47.93 67.95
Case fatality at 5-years (%) 7.14 0.00 16.67

Longitudinal metrics

All Female Male
Median nb. of events per indiv. 1.0 1.0 1.5
Recurrence at 6 months (%) 14.29 - 33.33

Survival analyses between endpoints

Plot

before Congenital and developmental myasthenia
after Congenital and developmental myasthenia

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Drugs most likely to be purchased after Congenital and developmental myasthenia