retinal ischemia

Sickle Cell Anemia

Clinical Characteristics
Ocular Features: 

The majority of serious ocular manifestations in sickle cell anemia are secondary to red blood cell sickling under conditions of relative hypoxia or dehydration resulting in thrombosis of retinal vessels with secondary ischemia.  Thrombosis of the central retinal artery and vein may also occur.  Other vessels of the orbit tissue and orbital walls when involved can result in acute proptosis with restrictions to globe motion and severe vascular congestion.

The conjunctival vessels are often comma-shaped and sludging or boxcaring of vascular flow is evident in a majority (70-90%) of patients.  Anterior uveitis of a granulomatous nature and frank anterior segment ischemia may occur.  Hyphemas are sometimes seen and an associated elevated intraocular pressure is a major risk.

The retina and its responses to small vessel occlusive disease constitute a major threat to vision and the risk is higher in patients with SC disease.  In early disease only arteriolar occlusions are seen but the localized ischemia stimulates the formation of arteriovenous anastomoses.  The involvement of larger areas of ischemia results in frank neovascularization, often in a formation known as retinal sea fans.  Intravitreal bleeding results in vitreal fibrosis with retinal traction that may result in a detachment.

Retinal imaging reveals general thinning.  SD-OCT imaging shows this to be especially visible in the macula and is present early in the disease.  The temporal retina likewise has significant thinning and microperimetry may demonstrate decreased function in these areas.

Systemic Features: 

The term sickle cell anemia as generally used refers to the disease caused by homozygous mutations in the HBB gene in which both beta chains contain a change in the 6th position from glutamic acid to valine yielding hemoglobin S.  These cells are susceptible to distortion into a sickle shape under certain conditions such as relative dehydration or anoxia and, as a result, form microthrombi with downstream ischemia.

The term sickle cell disease is commonly used to refer to sickling disorders in which only one beta chain contains the S change and the other chain has another variant such as Hb C (Hb SC disease), beta thalassemia (Hb S beta thalassemia) or some other more rare change in the beta chain.  Symptoms of the variant diseases generally have a later onset and cause a less severe disease.

Hb SS disease accounts for 60-70% of sickle cell disease and often leads to symptoms in the first month of life.  The diagnosis is usually made through newborn screening programs and should be followed by confirmatory testing using genotyping within 6 weeks.

The major early symptom is intermittent pain which can be incapacitating.  This can occur in virtually any organ and results from vascular occlusion, especially in small vessels such as arterioles and capillaries with downstream microinfarctions and hemolysis.  These vasoocclusive episodes can eventually lead to organ failure, especially in adults in which the major causes of death by midlife are pulmonary hypertension, cerebrovascular events, and acute chest syndrome.  Children are more likely to die of infections and organ sequestration.  In particular, the spleen is damaged as early as 3 months of age leaving infants vulnerable to recurrent septicemia and meningitis.  Severe bone pain with osteomyelitis can be debilitating.  Priapism, anemia, and ischemic strokes can occur at any age but are especially worrisome in young children.

Sickle cell disease can damage any part of the body and global evaluations are recommended when the diagnosis is under consideration. 

Genetics

Sickle cell disease and sickle cell anemia are autosomal recessive disorders resulting from homozygous or compound heterozygous mutations in the genes that code for hemoglobin molecules.  Usually at least one beta chain contains the amino acid substitution of valine for glutamic acid at the 6 position.  The HBB gene is located at 11p15.4.

Pedigree: 
Autosomal recessive
Treatment
Treatment Options: 

In general, patients with SS and S-variant disease should avoid strenuous exercise, low oxygen environments, extreme cold, and dehydration. Avoidance of contact with others who may have infectious disease is always recommended.  Hydroxyurea therapy may lessen or prevent chronic pain but it has little value in the treatment of acute painful crises.  Specific organ treatment should be applied as indicated for acute episodes.  All patients with sickle disease need to be under lifelong surveillance.

Epsilon aminocaproic acid is especially useful in the management of hyphemas and reduces the risk of recurrence.  The usual treatment for subretinal neovascularization and retinal detachment may be applied.  Anterior segment disease must be appropriately treated.

More recent approaches that show some promise include stem-cell transplantation.

References
Article Title: 

Familial Exudative Vitreoretinopathy, EVR3

Clinical Characteristics
Ocular Features: 

Abnormal retinal angiogenesis with retinal ischemia is the development defect that leads to the clinical features of the familial exudative vitreoretinopathies.  It is usually bilateral.  There is considerable clinical heterogeneity in the appearance of both the retina and the vitreous but common to all is the presence of peripheral areas of avascularity in the retina that may be seen in newborns.  This may only be visible using fluorescein angiography in mild cases.  The vessels may be hyperpermeable resulting in patchy exudates in the retina.  Neovascularization often develops with retinal and vitreous bleeding and eventually retinal traction resulting in retinal folds and detachments. Severe disease with early onset may result in blindness in infants but milder disease may be asymptomatic even as adults.  Cataracts may result.

The ocular disease may be confused with retinal dysplasia (as seen in pseudogliomas and Norrie disease [310600]) or retinopathy of prematurity.

Systemic Features: 

 No systemic features have been reported in EVR3.

Genetics

This is likely an autosomal dominant disorder based on pedigree evidence but no specific mutation has been found.  A disease locus at 11p13-p12 has been identified by linkage studies, located near the FZD4 gene containing the mutation responsible for EVR1.

Pedigree: 
Autosomal dominant
Treatment
Treatment Options: 

Appropriate vitreoretinal surgery to release vitreous traction and to repair retinal detachments should be considered.  Cataract removal may be beneficial.  Low vision aids could be helpful in milder cases with residual vision.

References
Article Title: 

Familial Exudative Vitreoretinopathy, EVR2

Clinical Characteristics
Ocular Features: 

The basis for many of the ocular complications likely begins with incomplete development of the retinal vasculature.  Resulting retinal ischemia leads to neovascularization, vitreous hemorrhage and traction, and retinal folds, with some 20% going on to develop rhegmatogenous or traction detachments.  There is, however, considerable clinical variability, even within families, with some infants blind from birth whereas some (41%) adults have only areas of remaining avascularity or evidence of macular dragging.  In fact, some affected individuals are asymptomatic and diagnosed only as part of extensive family studies.  Intraretinal lipid is often seen.  Considerable asymmetry in the two eyes is common.  Secondary cataracts often occur and phthisis bulbi results in some patients.  The clinical picture is sometimes confused with retinopathy of prematurity.

Systemic Features: 

No consistent systemic abnormalities have been identified in EVR2.

Genetics

Familial exudative vitreoretinopathy is the name given to a clinically and genetically heterogeneous group of disorders caused by mutations in several genes.  Autosomal dominant (e.g., EVR1; 133780), and X-linked inheritance (this condition) have been reported with the former much more common. 

The X-linked form of FEVR (EVR2 described here) results from mutations in the NDP gene (Xp11.3) and is allelic to Norrie disease (310600).

Retinopathy of prematurity can be called a phenocopy of FEVR.

Pedigree: 
X-linked recessive, carrier mother
X-linked recessive, father affected
Treatment
Treatment Options: 

Retinal, vitreal, and cataract surgery are indicated in appropriate cases.

References
Article Title: 

Familial Exudative Vitreoretinopathy, EVR4

Clinical Characteristics
Ocular Features: 

The basis for many of the ocular complications likely begins with incomplete development of the retinal vasculature.  Resulting retinal ischemia leads to neovascularization, vitreous hemorrhage and traction, and retinal folds with some 20% going on to develop rhegmatogenous or traction detachments.  There is, however, considerable clinical variability, even within families, with some infants blind from birth whereas some (41%) adults have only areas of remaining avascularity or evidence of macular dragging.  In fact, some affected individuals are asymptomatic and diagnosed only as part of extensive family studies.  Intraretinal lipid is often seen.  Considerable asymmetry in the two eyes is common. Secondary cataracts often occur and phthisis bulbi results in some patients.  The clinical picture is sometimes confused with retinopathy of prematurity.

Systemic Features: 

Osteoporosis and endosteal hyperostosis has been reported among individuals with mutations in LRP5.

Genetics

The EVR4 form of FEVR results from mutations in the LRP5 gene (11q13.4) and the clinical features may be seen in both heterozygotes and homozygotes.  Thus the disease is inherited in both autosomal dominant and autosomal recessive patterns.  The osteoporosis-pseudoglioma syndrome (259770) is allelic to this condition.

Mutations in the FZD4 gene cause a phenotypically indistinguishable condition (EVR1; 133780) but is always inherited in an autosomal dominant pattern.  There is also an X-linked form (EVR2) caused by a mutation in NDP (305390).

Retinopathy of prematurity can be called a phenocopy of FEVR.

Pedigree: 
Autosomal dominant
Autosomal recessive
Treatment
Treatment Options: 

Retinal, vitreal, and cataract surgery are indicated in appropriate cases.

References
Article Title: 

Familial Exudative Vitreoretinopathy, EVR1

Clinical Characteristics
Ocular Features: 

The basis for many of the ocular complications likely begins with incomplete development of the retinal vasculature.  Resulting retinal ischemia leads to neovascularization, vitreous hemorrhage and traction, and retinal folds, with some 20% going on to develop rhegmatogenous or traction detachments.  There is, however, considerable clinical variability, even within families, with some infants blind from birth whereas some (41%) adults have only areas of remaining avascularity or evidence of macular dragging.  In fact, some affected individuals are asymptomatic and diagnosed only as part of extensive family studies.  Intraretinal lipid is often seen.  Considerable asymmetry in the two eyes is common.  Secondary cataracts often occur and phthisis bulbi results in some patients.  The clinical picture is sometimes confused with retinopathy of prematurity.

Systemic Features: 

No systemic features have been associated with EVR1 disease.

Genetics

Familial exudative vitreoretinopathy is the name given to a clinically and genetically heterogeneous group of disorders caused by mutations in several genes.  Both autosomal dominant (EVR1 described here) plus EVR4 (601813) and X-linked inheritance (EVR2; 305390) have been reported with the former much more common.  Similarities in the clinical presentation of Congenital Nonattachment of the Retina may cause diagnotic confusion. 

Mutations in the frizzled-4 gene FZD4 (11q14-q21) have been associated with the EVR1 form of this disease inherited in an autosomal dominant pattern.  Retinopathy of prematurity can be called a phenocopy of FEVR.

Pedigree: 
Autosomal dominant
Treatment
Treatment Options: 

Retinal, vitreal, and cataract surgery are indicated in appropriate cases.

References
Article Title: 
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