Wilson disease | Menke disease |
1. Autosomal recessive | 1. X linked recessive |
2. Mutation in the ATP7B gene | 2. Mutation in the ATP7A gene |
3. Defective copper excretion (Copper overload in body) | 3. Impaired copper absorption (Copper deficiency in body) |
Wilson disease | Menke disease |
1. Autosomal recessive | 1. X linked recessive |
2. Mutation in the ATP7B gene | 2. Mutation in the ATP7A gene |
3. Defective copper excretion (Copper overload in body) | 3. Impaired copper absorption (Copper deficiency in body) |
