Peters plus syndrome and Chorioretinal findings associated with B3GLCT gene mutation - a case report

Peters plus syndrome (PPS, also known as Krause-Kivlin or Krause-van Schooneveld-Kivlin syndrome) is characterized by eye abnormalities, characteristic facial features, cleft lip/palate, short limbs with brachydactyly, and developmental delay with intellectual disability [1].

PPS is usually inherited in an autosomal recessive pattern due to biallelic mutations in B3GLCT (also known as B3GALTL), which is associated with an increased risk for miscarriages and stillbirth of affected fetuses [2‐4]. Systemic abnormalities may include congenital heart defects, genitourinary anomalies, structural brain malformations, congenital hypothyroidism, and conductive hearing loss [1, 3, 4].

Eye abnormalities in PPS predominantly involve the anterior segment, including corneal clouding, posterior cornea thinning, and iridocorneal adhesions. Based on the anatomic pathology, Peters anomaly may be classified as type I (without keratolenticular adhesion), or type II (with lens abnormalities) [4]. Other ophthalmological defects include iris coloboma and retrolental cyst, although no optical tomographic characterization of chorioretinal findings has been described [1, 5]. In this report, we characterize the chorioretinal findings in a patient with PPS with homozygous pathogenic B3GLCT mutation.

The patient is a 22-month-old Caucasian boy, born at 36 weeks by spontaneous vaginal delivery with normal prenatal care. He had no family history of glaucoma or anterior segment dysgenesis. At birth, he was noted to have bilateral cloudy corneas with no epiphora nor photophobia. He was started on presumptive treatment of topical dorzolamide 2% and hypertonic sodium chloride ophthalmic solution 5% prior to his presentation at the Bascom Palmer Eye Institute. A bedside eye exam revealed a “corneal opacity centrally sparing the periphery” and he was diagnosed with possible congenital glaucoma associated with Peters anomaly. Extraocular findings included short extremities and brachydactyly, cleft palate, characteristic facial features, developmental delay, and pulmonary stenosis (Table 1).

An exam under anesthesia (EUA) was performed the same day. Intraocular pressures (IOP) were 32 mmHg and 27 mmHg in the right eye (OD) and left eye (OS), respectively (Tono-Pen XL, Reichert Inc. Depew, NY). Bright red reflexes were noted prior to dilation in both eyes (OU). Other ocular abnormalities included iridocorneal adhesion superiorly OS and posterior capsular cataract OU. Given the absence of limbal enlargement, normal axial lengths, and an intact red reflex prior to dilation, glaucoma surgery was deferred. Phenylephrine 2.5% OU was added for optical dilation and visual rehabilitation, and topical dorzolamide 2% was continued.

In the subsequent serial EUA, more adhesions between the iris and cornea OS were noted despite the generally improved corneal opacities OU. Posterior segment improved as the media opacity cleared. Fluorescein angiography (FA) was performed (RetCam3, Ophthalmic Imaging System, Natus Medical), and spectral-domain optical coherence tomography (SD-OCT) images were obtain (Spectralis flex module, Heidelberg Engineering). The optic discs were noted to have morning glory-like appearances suggestive of colobomatous changes, with a cup to disc ratio of approximately 0.7 OU. Diffuse chorioretinal atrophies were noted [Fig. 1a-b]. The right eye had a well-defined white-yellowish, comet shaped lesion along the superotemporal arcade [Fig. 1 a]. A similar lesion that was well-circumscribed, oval-shaped and atrophic was seen in the central macula of the left eye [Fig. 1 b]. FA demonstrated early hyperfluorescence of the lesion with no leakage in the right eye, and early hyperfluorescence secondary to a window defect corresponding to the macular lesion in the left eye. Late frames of the FA showed hyperfluorescence of the atrophic lesions [Fig. 1 c-d]. There were neither leakage from the optic disc, nor vascular abnormalities in the peripheral retina. Intraoperative SD-OCT of the macula showed severe diffuse thinning of the retina and choroid in the atrophic lesions. Additionally, in the left eye oval shaped atrophic lesion, a complete loss of retinal structure was noted [Fig. 1E-F]. Written informed consent to publish the acquired images were obtained from the patient’s guardians.

In this case report, we used multimodal imaging to characterize the bilateral chorioretinal lesions in a young patient with PPS associated with a homozygous B3GLCT mutation. Both eyes had diffuse chorioretinal atrophy, with very well-defined areas of thinning/absence of the retina layers located in the posterior pole. Reis et al. described a retinal coloboma-like lesion in a premature PPS patient with B3GLCT mutation [6]. However, the lesion was not further characterized in their report [6]. Weh and colleagues reported one patient with chorioretinal changes in their cohort of 9 PPS patients with B3GLCT mutations, but a detailed description of the lesion was similarly not presented [7].

The B3GLCT gene (chromosome 13) was identified by Heinonen et al. and encodes a glucosyltransferase protein which catalyzes glycosylation of other proteins [8]. This protein mediates the non-canonical endoplasmic reticulum quality-control mechanism, which involves identifying and stabilizing properly folded proteins through glycosylation [9]. As of 2019, all 15 B3GLCT mutations reported in the literature (including c.660 + 1G > A, the most common allele) were predicted to cause truncated protein products that result in complete loss of function [6, 10]. The B3GLCT gene transcripts have been found in various human tissues including the heart, kidney, and brain [8, 11]. A loss of function mutation in B3GLCT gene likely causes malfunctioning in protein glycosylation resulting in anomalies of multiple organ systems [8, 11]. The mechanism resulting in the chorioretinal findings remain uncertain.