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Pigmented paravenous retinochoroidal atrophy(PPCRA)

MedGen UID:
401413
Concept ID:
C1868310
Disease or Syndrome
Synonym: Pigmented paravenous chorioretinal atrophy
SNOMED CT: Pigmented paravenous retinochoroidal atrophy (723450004); Pigmented paravenous chorioretinal atrophy (723450004); PPRCA - pigmented paravenous retinochoroidal atrophy (723450004)
Modes of inheritance:
Autosomal dominant inheritance
MedGen UID:
141047
Concept ID:
C0443147
Intellectual Product
Source: Orphanet
A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.
Not genetically inherited
MedGen UID:
988794
Concept ID:
CN307044
Finding
Source: Orphanet
clinical entity without genetic inheritance.
 
Gene (location): CRB1 (1q31.3)
 
Monarch Initiative: MONDO:0008246
OMIM®: 172870
Orphanet: ORPHA251295

Definition

Pigmented paravenous chorioretinal atrophy is a stationary disease of the ocular fundus in which bone corpuscle pigmentation is seen in a paravenous distribution. Patients are usually asymptomatic; diagnosis is based on the characteristic fundus appearance. Most cases have been reported in males (summary by Traboulsi and Maumenee, 1986). [from OMIM]

Clinical features

From HPO
Esotropia
MedGen UID:
4550
Concept ID:
C0014877
Disease or Syndrome
A form of strabismus with one or both eyes turned inward ('crossed') to a relatively severe degree, usually defined as 10 diopters or more.
Hypermetropia
MedGen UID:
43780
Concept ID:
C0020490
Disease or Syndrome
An abnormality of refraction characterized by the ability to see objects in the distance clearly, while objects nearby appear blurry.
Vitreoretinopathy
MedGen UID:
87480
Concept ID:
C0344290
Disease or Syndrome
Ocular abnormality characterized by premature degeneration of the vitreous and the retina that may be associated with increased risk of retinal detachment.
Bone spicule pigmentation of the retina
MedGen UID:
323029
Concept ID:
C1836926
Finding
Pigment migration into the retina in a bone-spicule configuration (resembling the nucleated cells within the lacuna of bone).
Paravenous chorioretinal atrophy
MedGen UID:
893102
Concept ID:
C4072868
Disease or Syndrome
Chorioretinal atrophy along the retinal veins.

Recent clinical studies

Etiology

Takagi S, Hirami Y, Takahashi M, Yamamoto S, Goto S, Yamamoto M, Fujihara M, Tomita G, Kurimoto Y
Ophthalmol Retina 2018 Jan;2(1):79-81. Epub 2017 Jul 26 doi: 10.1016/j.oret.2017.05.004. PMID: 31047313
Choi JY, Sandberg MA, Berson EL
Am J Ophthalmol 2006 Apr;141(4):763-5. doi: 10.1016/j.ajo.2005.11.009. PMID: 16564825
Yanagi Y, Okajima O, Mori M
Acta Ophthalmol Scand 2003 Feb;81(1):60-7. doi: 10.1034/j.1600-0420.2003.00003.x. PMID: 12631022
Murray AT, Kirkby GR
Eye (Lond) 2000 Oct;14 Pt 5:711-6. doi: 10.1038/eye.2000.189. PMID: 11116690

Diagnosis

Castaño Silos JC, Sanchez-Guillen I, Almorín-Fernández-Vigo I, Jerez Fidalgo M, Fernández-Vigo JI
Arch Soc Esp Oftalmol (Engl Ed) 2023 Apr;98(4):233-237. Epub 2023 Feb 15 doi: 10.1016/j.oftale.2022.12.003. PMID: 36801254
Ranjan R, Jain M A, Verghese S, Manayath GJ, Narendran V
Eur J Ophthalmol 2022 Jan;32(1):NP125-NP129. Epub 2020 Oct 23 doi: 10.1177/1120672120965489. PMID: 33092398
Jung I, Lee Y, Kang S, Won J
Medicina (Kaunas) 2021 Dec 19;57(12) doi: 10.3390/medicina57121382. PMID: 34946327Free PMC Article
Deshmukh S, Das D, Deka H, Bhattacharjee H, Upadhyay A, Gupta K
Indian J Ophthalmol 2019 Feb;67(2):271-273. doi: 10.4103/ijo.IJO_1202_18. PMID: 30672488Free PMC Article
Lenci LT, Parke DW 3rd, Almeida DR
Ophthalmology 2016 Oct;123(10):2112. doi: 10.1016/j.ophtha.2016.04.052. PMID: 27664911

Therapy

Figueiredo R, Morais Sarmento T, Garrido J, Ramalho A
BMJ Case Rep 2019 Aug 10;12(8) doi: 10.1136/bcr-2019-230633. PMID: 31401582Free PMC Article

Prognosis

Castaño Silos JC, Sanchez-Guillen I, Almorín-Fernández-Vigo I, Jerez Fidalgo M, Fernández-Vigo JI
Arch Soc Esp Oftalmol (Engl Ed) 2023 Apr;98(4):233-237. Epub 2023 Feb 15 doi: 10.1016/j.oftale.2022.12.003. PMID: 36801254
Jung I, Lee Y, Kang S, Won J
Medicina (Kaunas) 2021 Dec 19;57(12) doi: 10.3390/medicina57121382. PMID: 34946327Free PMC Article
Murray AT, Kirkby GR
Eye (Lond) 2000 Oct;14 Pt 5:711-6. doi: 10.1038/eye.2000.189. PMID: 11116690
Brooks DN, Potter JW, Bartlett JD, Nowakowski R
J Am Optom Assoc 1980 Dec;51(12):1097-1101. PMID: 7204821
Miller SA, Stevens TS, Myers F, Nieder M
Ann Ophthalmol 1978 Jul;10(7):867-71. PMID: 677665

Clinical prediction guides

Menteş J, Değirmenci C
Turk J Ophthalmol 2022 Dec 28;52(6):432-435. doi: 10.4274/tjo.galenos.2022.39032. PMID: 36578225Free PMC Article
Oh JK, Nuzbrokh Y, Lee W, Lima de Carvalho JR Jr, Wang NK, Sparrow JR, Allikmets R, Tsang SH
Eur J Ophthalmol 2022 Jan;32(1):NP235-NP239. Epub 2020 Sep 14 doi: 10.1177/1120672120957599. PMID: 32927963Free PMC Article
Jung I, Lee Y, Kang S, Won J
Medicina (Kaunas) 2021 Dec 19;57(12) doi: 10.3390/medicina57121382. PMID: 34946327Free PMC Article
Murray AT, Kirkby GR
Eye (Lond) 2000 Oct;14 Pt 5:711-6. doi: 10.1038/eye.2000.189. PMID: 11116690
Brooks DN, Potter JW, Bartlett JD, Nowakowski R
J Am Optom Assoc 1980 Dec;51(12):1097-1101. PMID: 7204821

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