Unilateral Retinitis Pigmentosa Sine Pigmento

Retinitis Pigmentosa Sine Pigmento Masquerading as Normal Tension Glaucoma

“…RP is usually a bilateral disease, but unilateral cases have been reported. 1,2 We have also documented, from our patient, that progression from "normal" fundal appearance to a phase with vessel attenuation, disk pallor and rapid visual field progression can occur within a year's time for unilateral RP sine pigmento.…”

Retinitis Pigmentosa Sine Pigmento Masquerading as Normal Tension Glaucoma

“…RP is usually a bilateral disease, but unilateral cases have been reported. 1,2 We have also documented, from our patient, that progression from "normal" fundal appearance to a phase with vessel attenuation, disk pallor and rapid visual field progression can occur within a year's time for unilateral RP sine pigmento.…”

Glare sensitivity and professional drivers' safety: a case of rod‐cone dystrophy with negative electroretinogram

“…A special form of rod-cone dystrophy or retinitis pigmentosa sine pigmento like the one found in our patient, without the typical bone spicule-like deposits, has been described by Gordon (1953) and a unilateral form by Jacobson & Stephens 1962). The diagnosis of these changes is often complicated and delayed by the absence of fundus changes and initially mild relative scotomata in the midperiphery.…”

Unilateral pigmentary retinopathy: a retrospective case series

“…Three patients had unilateral hypopigmentation similar to that described in older literature as 'RP sine pigmento' (Jacobson & Stephens 1962;Pearlman et al 1976), but which is unlikely to be a distinct diagnostic entity. Fundus examination and/or FAF imaging revealed restricted abnormality in 6 cases, none with a definite diagnosis.…”

“…Three patients had unilateral hypopigmentation similar to that described in older literature as ‘RP sine pigmento’ (Jacobson & Stephens ; Pearlman et al. ), but which is unlikely to be a distinct diagnostic entity.…”

Retinitis Pigmentosa Sine Pigmento Masquerading as Normal Tension Glaucoma

“…RP is usually a bilateral disease, but unilateral cases have been reported. 1,2 We have also documented, from our patient, that progression from "normal" fundal appearance to a phase with vessel attenuation, disk pallor and rapid visual field progression can occur within a year's time for unilateral RP sine pigmento.…”

Glare sensitivity and professional drivers' safety: a case of rod‐cone dystrophy with negative electroretinogram

“…A special form of rod-cone dystrophy or retinitis pigmentosa sine pigmento like the one found in our patient, without the typical bone spicule-like deposits, has been described by Gordon (1953) and a unilateral form by Jacobson & Stephens 1962). The diagnosis of these changes is often complicated and delayed by the absence of fundus changes and initially mild relative scotomata in the midperiphery.…”

Unilateral pigmentary retinopathy: a retrospective case series

“…Three patients had unilateral hypopigmentation similar to that described in older literature as 'RP sine pigmento' (Jacobson & Stephens 1962;Pearlman et al 1976), but which is unlikely to be a distinct diagnostic entity. Fundus examination and/or FAF imaging revealed restricted abnormality in 6 cases, none with a definite diagnosis.…”

“…Three patients had unilateral hypopigmentation similar to that described in older literature as ‘RP sine pigmento’ (Jacobson & Stephens ; Pearlman et al. ), but which is unlikely to be a distinct diagnostic entity.…”

Retinitis Pigmentosa Sine Pigmento Masquerading as Normal Tension Glaucoma

“…RP is usually a bilateral disease, but unilateral cases have been reported. 1,2 We have also documented, from our patient, that progression from "normal" fundal appearance to a phase with vessel attenuation, disk pallor and rapid visual field progression can occur within a year's time for unilateral RP sine pigmento.…”

Glare sensitivity and professional drivers' safety: a case of rod‐cone dystrophy with negative electroretinogram

“…A special form of rod-cone dystrophy or retinitis pigmentosa sine pigmento like the one found in our patient, without the typical bone spicule-like deposits, has been described by Gordon (1953) and a unilateral form by Jacobson & Stephens 1962). The diagnosis of these changes is often complicated and delayed by the absence of fundus changes and initially mild relative scotomata in the midperiphery.…”

Unilateral pigmentary retinopathy: a retrospective case series

“…Three patients had unilateral hypopigmentation similar to that described in older literature as 'RP sine pigmento' (Jacobson & Stephens 1962;Pearlman et al 1976), but which is unlikely to be a distinct diagnostic entity. Fundus examination and/or FAF imaging revealed restricted abnormality in 6 cases, none with a definite diagnosis.…”

“…Three patients had unilateral hypopigmentation similar to that described in older literature as ‘RP sine pigmento’ (Jacobson & Stephens ; Pearlman et al. ), but which is unlikely to be a distinct diagnostic entity.…”