Coat’s like vasculopathy in leber congenital amaurosis secondary to homozygous mutations in CRB1: a case report and discussion of the management options

Background Mutations in the CRB1 gene are associated with variable phenotypes of severe retinal dystrophies, and retinal dystrophies resulting from CRB1 mutations may be accompanied by specific fundus features such as coat’s like vasculopathy in retinitis pigmentosa patients. This is the first report of the occurrence of coat’s like vasculopathy in a patient diagnosed with Leber congenital amaurosis caused by a CRB1 mutation. Case presentation An 18-year old Syrian female patient presented with bilateral gradual loss of vision since early childhood, with recent deterioration in her left eye. She appeared to have an asymmetric bilateral coat’s like vasculopathy which was more severe in the left eye. The diagnosis of Leber congenital amaurosis was suggested, and a genetic CRB1 sequencing for the patient and her two younger siblings, who also had severe vision loss, was done, upon which the diagnosis of Leber congenital amaurosis associated with exudative retinal detachment due to coat’s like vasculopathy was made. Treatment with panretinal photocoagulation was attempted in the worse left eye, but with no improvement. As the disease suddenly progressed in both eyes, pars plana vitrectomy with endolaser and silicone oil tamponade was performed in the better right eye which led to anatomical stabilization of the case without improvement in the visual acuity. Conclusion Leber congenital amaurosis is reported to be associated with multiple systemic and ocular findings, none of which is coat’s like vasculopathy. CRB1 gene mutations are associated with remarkable retinal findings in patients with retinitis pigmentosa and other fundus dystrophies. In this unique case we are reporting the incidence of coat’s like vasculopathy in a patient diagnosed with Leber congenital amaurosis caused by CRB1 gene mutation, and its management. CRB1 mutant patients should be followed up closely as sudden progression can have permanent poor outcomes and as early management is vital in such cases.


Background
Originally described by Theodore Leber in 1869 [1], Leber congenital amaurosis (LCA; MIM# 204000) is the earliest and most severe form of all hereditary retinal dystrophies, responsible for congenital blindness [1].
LCA accounts for at least 5 % of all retinal dystrophies and is one of the main causes of blindness in children [2].
The clinical features of LCA patients usually include roving eye movements/nystagmus, digito-ocular signs (eye poking or rubbing), an apparently normal or saltand-pepper pigmented fundus and severely reduced or absent scotopic and photopic electroretinogram (ERG), Although it is an early-onset and severe disease, LCA has a variable expression, which may reflect, at least in part, its high genetic heterogeneity [3].

BMC Research Notes
*Correspondence: somerh@gmail.com 1 Department of Ophthalmology, Damascus University, Almouassat University Hospital, Damascus, Syria Full list of author information is available at the end of the article Mutations in the CRB1 gene are one of the at least 17 known gene mutations that are accused to cause LCA, and CRB1 mutations are associated with variable phenotypes of severe retinal dystrophies, ranging from LCA to rod-cone dystrophy [also called retinitis pigmentosa (RP)]. Moreover, RP resulting from CRB1 mutations may be accompanied by specific fundus features: preservation of the para-arteriolar retinal pigment epithelium (PPRPE) and retinal telangiectasia with exudation (also referred to as coats-like vasculopathy) [4], which is a well-known, although rare, complication of RP [5].
In severe cases this disorder may progress to total retinal detachment and visual loss in the context of longstanding RP [5]. CRB1 mutations were reported in a significant proportion of patients with coat's like RP as high as 55 % [6].
In this case, we report the (first) occurrence of coat's like vasculopathy in a patient diagnosed with LCA caused by a CRB1 mutation.

Case presentation
An 18 year old Syrian female, daughter of first-cousins parents, presented with recent deterioration of visual acuity in her left eye, she reported a history of decreased vision bilaterally that started many (undefined) years ago. Visual acuity was (OD: 0.16) and (OS: Perception of light), examination revealed marked relative afferent pupillary defect (RAPD) in the left eye, cycloplegic refraction was OD: +8.00(−1.50X70) and OS: +10.50(−1.25X15), Axial length measurements were: OD: 18.80 mm and OS: 19.10 mm. Cornea and anterior segment examination was within normal limits and dilated fundus examination revealed: OD: abnormal foveal reflex (Fig. 1a), peripheral nummular pigmentations in the superior attached retina (Fig. 1b) and infero-temporal exudative retinal detachment not threatening the macula, with severe telangiectasia and very dense hard exudates all over the inferior detached retina. Fluorescein angiography (FA) (Fig. 1c, d) revealed areas of capillary non-perfusion with diffuse capillary and focal leakage in the areas of abnormal vessels with extensive leakage in late phases.
OS: mildly elevated subtotal exudative retinal detachment with extensive hard exudates and telangiectatic vessels all over the detached retina, with the same pigmented patches noted in the right eye ( Fig. 2a, b). FA revealed extensive leakage beginning from the early phases and continuing during the whole study time (Fig. 2c, d).
ERG revealed severely reduced scotopic and photopic responses; suggestive of a severe form of rod-cone dystrophy consistent with LCA. Ocular coherence tomography (OCT) revealed serous retinal detachment involving the fovea in left eye.
Examination of family members revealed two younger male siblings (12 years old, and 2 years old) having profound visual loss. The clinical presentation of the two siblings is presented in Table 1, and it was suggestive of LCA, one more sibling (8 years old male) and the two parents revealed no ocular abnormalities.
CRB1 mutation was suspected to be responsible for the pathologic presentations of the patients, and gene sequencing was performed searching for mutations in the entire coding sequence of the CRB1 gene using fluorescent sequencing, which revealed that the three siblings share the same variant c.2555T >C (p.I852T) in the homozygous state. Accordingly, diagnosis of LCA8 was confirmed in the three siblings.
As there are no definitive guidelines for the management of coat's like vasculopathy associated with retinal dystrophies, decision was made to perform pan-retinal photocoagulation (PRP) over the inferior detached retina in the left eye with close follow up, and only close follow up in the right eye as the parents refused any type of management in the better seeing eye. The retinal detachment remained stable over the following 6 weeks. On the eighth week post laser the patient complained of sudden decrease of visual acuity in her better right untreated eye to perception of light (PL) with no right projection, and to no perception of light (NPL) in the left previously treated eye. The decision to perform pars plana vitrectomy (PPV) for the right eye was made, advantages and disadvantages of surgical treatment were explained to the patient and parents and informed consent was taken. Standard PPV with extensive intraoperative PRP was done with the use of silicone oil tamponade at the end of surgery. No surgical treatment was done for the left eye as the patient refused surgery for this eye.
Over 6 months follow up period, the retina of the right eye remained attached with no improvement in visual acuity (perception of light with no light projection), while the left eye continued to have subtotal retinal detachment, which appeared to increase in height and finally developed neovascular glaucoma.

Discussion
LCA is the earliest and most severe form of all inherited retinal dystrophies, characterized by blindness or severe visual impairment from birth [2]. LCA has a variable expression which may reflect, at least in part, its high genetic heterogeneity, disease-associated mutations have been reported in at least seventeen genes including: GUCY2D, CRB1, RPE65, RPGRIP1, AIPL1, TULP1 and CRX [6]. Crumbs homologue 1 (CRB1) is homologous to the Drosophila Crumbs protein and Drosophila Crumbs is essential for establishing and maintaining apico-basal polarity in embryonic epithelia derived from the ectoderm. In particular, Crumbs is required for the biogenesis of the zonula adherens, a belt-like structure encircling the apex of epithelial cells [2].
CRB1 mutations are the second most common gene mutations found among LCA patients, accounting for 7.4-10 % of all LCA patients [7,8], and mutations in the CRB1 gene are associated with variable phenotypes of severe retinal dystrophies, ranging from LCA to RP.
The association of coat's like vasculopathy and RP is extensively studied, a complication that is estimated to be found in 1.2-3.6 % of all RP patients [5]. CRB1 mutations were found in about 55 % of these patients [6], suggesting that CRB1 mutations should be considered an important risk factor for the coats-like reaction in RP patients, although its development may require additional genetic or environmental factors [6]. On the other hand, the presence of coat's like vasculopathy is highly suggestive of a CRB1 mutation, and CRB1 sequencing may be warranted in these patients.
Our patient presented with bilateral asymmetric coat's like picture, high hyperopia, posterior microphthalmos and severely reduced scotopic and photopic ERG responses which was suggestive of a severe retinal dystrophy. This presentation suggested that CRB1 may be the responsible gene. CRB1 gene sequencing for the patient and her affected siblings revealed a homozygote state of the variant c.2555T >C (p.I852T).
This same mutation was mentioned in the literature by Francesca Simonelli et al. [8] who thoroughly studied 95 patients with LCA, and found CRB1 mutations in 7.4 % of them, with the same p.I852T mutation (of our patients) in two patients of Italian ancestry, who were 40 and 45 years old and had severe loss of vision: perception of light in the first and hand movement in the second. In addition both patients had cycloplegic refraction of about +4.00 diopters and ERG responses compatible with Rod-Cone dystrophy. The two patients in Simonelli study were described to have "retinitis pigmentosa fundus findings", Searching the literature for suggested management of patients having coat's like disease and RP revealed multiple management plans including: vitrectomy and endolaser [9], cryotherapy, scleral buckling with subretinal fluid  drainage and laser photocoagulation of the telangiectatic and neovascular lesions [10] and intravitreal dexamethasone implant [11]. Our patient was managed initially with PRP over the detached retina in the worse (left) eye as the detachment was not involving the macula. Later as the case progressed to total retinal detachment in both eyes with the right eye being the better one, a PPV, endolaser and silicone oil tamponade was done for the right eye trying to reattach the retina with resultant anatomical stabilization defined by maintaining attached retina and prevention of neovascular glaucoma in this eye, which was encountered in the other non-operated eye. Retinal reattachment was not accompanied with any improvement in visual function or restoring the previous vision.
We suggest PPV with extensive endolaser to be considered early in the course of such patients as the severe

Conclusion
CRB1 gene mutation is a very well known risk factor for the development of coat's like vasculopathy in RP patients, and our case presents the co-existence of the coat's like reaction and LCA in a patient with CRB1 mutation, it is not obvious whether this mutation is responsible for the coat's reaction as it was also described in other patients without causing the coat's exudate.
LCA has a very guarded prognosis, but it can be even worse when a complication such as coat's like vasculopathy accompanies the case. We suggest close follow up for all LCA patients who have CRB1 mutations, especially the c.2555T >C (p.I852T) homozygote variant searching for any vascular abnormality and managing it as soon as it is diagnosed with PPV and endolaser in an attempt to halt the complete loss of the already severely affected visual function, preserve the eye and prevent neovascular glaucoma and painful blind eye.