रेटिनाइटिस पिगमेंटोसा

विवरण

Retinitis pigmentosa is a group of related eye disorders that cause progressive vision loss. These disorders affect the retina, which is the layer of light-sensitive tissue at the back of the eye. In people with retinitis pigmentosa, vision loss occurs as the light-sensing cells of the retina gradually deteriorate.

The first sign of retinitis pigmentosa is usually a loss of night vision, which becomes apparent in childhood. Problems with night vision can make it difficult to navigate in low light. Later, the disease causes blind spots to develop in the side (peripheral) vision. Over time, these blind spots merge to produce tunnel vision. The disease progresses over years or decades to affect central vision, which is needed for detailed tasks such as reading, driving, and recognizing faces. In adulthood, many people with retinitis pigmentosa become legally blind.

The signs and symptoms of retinitis pigmentosa are most often limited to vision loss. When the disorder occurs by itself, it is described as nonsyndromic. Researchers have identified several major types of nonsyndromic retinitis pigmentosa, which are usually distinguished by their pattern of inheritance: autosomal dominant, autosomal recessive, or X-linked.

Less commonly, retinitis pigmentosa occurs as part of syndromes that affect other organs and tissues in the body. These forms of the disease are described as syndromic. The most common form of syndromic retinitis pigmentosa is Usher syndrome, which is characterised by the combination of vision loss and hearing loss beginning early in life. Retinitis pigmentosa is also a feature of several other genetic syndromes, including Bardet-Biedl syndrome; Refsum disease; and neuropathy, ataxia, and retinitis pigmentosa (NARP).

Inheritance patterns

The source lists the following possible inheritance patterns: Autosomal recessive; Autosomal dominant; X-linked recessive. More than one pattern can apply in different cases.

Related genes

• USH2A

• CLRN1

• PRPH2

• BEST1

• CRB1

• RPE65

• RHO

• RPGR

• RP2

• ABCA4

• PDE6B

• WDR19

• CRX

• CA4

• CNGB1

• CNGA1

• GUCA1B

• IDH3B

• IMPDH1

• MT-TS2

• NRL

• PDE6A

• PDE6G

• RBP3

• RGR

• RLBP1

• ROM1

• RP9

• RP1

• SAG

• TULP1

• PROM1

• PRPF3

• LRAT

• NR2E3

• TOPORS

• MERTK

• SEMA4A

• PRPF8

• SNRNP200

• FSCN2

• PRPF31

• IMPG2

• SPATA7

• KLHL7

• FAM161A

• TTC8

• ZNF513

• RDH12

• EYS

• CERKL

• PCARE

• PRCD

Other names

Pigmentary retinopathy

Rod-cone dystrophy

RP

Tapetoretinal degeneration