Autozomálně recesivní
Caused by changes in both copies of PROM1 (prominin-1). Recessive variants cause a more severe panretinal dystrophy than dominant PROM1 variants, which mainly affect the macula.
Příznaky a projevy
Reduced vision with early macular involvement and panretinal dystrophy is typical in the recessive form, and a severe form of recessive retinitis pigmentosa has been described.
Co se diagnózou změní
Regular eye review, low-vision aids and educational support. Carrier testing of relatives and genetic counselling are available.
Analyzované geny
Zahrnuje 1 příbuzný podtyp ↓Skrýt podtypy ↑
- retinitis pigmentosa 41
