Sección: Congenital Defects

Methylmalonic Acidemia with Homocystinuria Type CbLC

Methylmalonic acidemia with homocystinuria is a congenital error in metabolism, consisting of an inability to convert vitamin B12 (cobalamin) into its

Retinal dystrophy associated with mutation in the HK1 gene

Retinitis pigmentosa is a diffuse and hereditary retinal dystrophy that affects photoreceptors, initially rods and later cones (rod-cone dystrophy). T