Journal of Ophthalmology

Journal of Ophthalmology / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 5069765 | 7 pages |

Clinical and Ultrastructural Studies of Gelatinous Drop-Like Corneal Dystrophy (GDLD) of a Patient with TACSTD2 Gene Mutation

Academic Editor: Tomasz Zarnowski
Received01 May 2019
Accepted22 Jul 2019
Published20 Aug 2019


Purpose. To describe clinical, molecular genetics, histopathologic and ultrastructural findings of gelatinous drop-like corneal dystrophy (GDLD) (OMIM #204870) in a Sudanese patient. Method. An ocular examination revealed the onset of GDLD in a Sudanese patient (50 years old) at King Khalid Specialist Hospital, Riyadh. The 333 sequence variants in 13 GDLD genes of a DNA sample were screened by Asper Ophthalmics Ltd. It was further confirmed by sequencing. The patient had undergone a penetrating keratoplasty in the right eye. The corneal tissue was processed for histopathology and ultrastructural studies. Results. Slit-lamp observation showed grayish-white multiple superficial corneal nodules of various sizes in the left and right eye. Both corneas became clear after the surgery. The GDLD deposits in the subepithelial region and in the anterior stroma were confirmed by PAS staining and their apple-green birefringence under polarized light. Ultrastructurally, the amyloid fibrils were very thin and grouped in whorl-like structures, which caused splits between and within the stromal lamellae. Collagen fibrils (CFs) and keratocytes had degenerated. A homozygous c.355T > A mutation in exon 1 of the TACSTD2 (M1S1) gene was detected, and alteration of the amino acid (p.Cysl19Ser in NCBI entry NP_002344.2) was observed. Conclusion. In our patient with GDLD, a “c.355T > A” mutation in exon 1 of TACSTD2 was detected and believed to be responsible for the alteration of the amino acid leading to the formation of the amyloid deposits. The deposits caused the ultrastructural degeneration of epithelium, Bowman’s layer, stroma, and keratocytes of the GDLD cornea.

1. Introduction

Gelatinous drop-like corneal dystrophy (GDLD; OMIM #204870) is characterized by the presence of multiple, gelatinous-like deposits in the subepithelial and stromal region of the cornea. The formation of the gelatinous lesions is due to deposition of amyloid in the superficial cornea [1, 2]. The deposits spread within the stroma leading to the impairment of vision. GDLD is an inherited ocular disease, which manifests commonly within the first-second decade of life (8 to 18 years). Nakaizaumi [1] was the first to describe it as gelatinous drop-like dystrophy, in Japan.

GDLD is caused by a mutation in the tumor-associated calcium signal transductor 2 (TACTD2) gene which is located on the short-arm of chromosome 1 [3, 4]. The disease is relatively common in Japan (1 in 333,000) but also occurs in other parts of the world such as India, China, and Europe [38]. Markoff et al. [8] reported the occurrence of GDLD in one Turkish family. The authors investigated bilateral GDLD corneal amyloidosis in two teenage girls (8 and 13 year) and showed a novel TACSTD2 mutation, c.653delA, occurred in both patients. Alavi et al. [9] have investigated mutations in 13 Iranian families with GDLD and found an association with four mutations in TACSTD2 (C66X, F114C, L186, and E227) with GDLD. The mutations C66X, F114C, and L186 were novel, whereas E227K was common among the members of the 10 families.

There are few studies carried out on the ultrastructure of the lamellae, collagen fibrils, and proteoglycans of the GDLD cornea. It has been noted that, in the early stage of GDLD, the basal lamina and Bowman’s layer (BW) are intact, but in the later stages, basal epithelial cells and basal lamina degenerate [10]. Kinoshita et al. [11] reported the presence of amyloid deposits in between the collagen fibrils of the stroma causing degeneration and disorganization of stromal collagen fibrils (CFs). Büchi et al. [12] reported that the amyloid deposits were mostly rounded and contained irregularly running amyloid fibrils of various thicknesses ranging from nanometers to the several microns. There was a large amount of lactoferrin and keratoepithelin (βig-h3) observed in the ultrastructural nodular deposits in the cornea of a child diagnosed with GDLD [13].

In the present study, we investigated the genetic, histopathological, and ultrastructure features of a Sudanese patient affected by GDLD. The patient was diagnosed at King Khalid Specialist Eye Hospital, Riyadh (to our knowledge, this is the first case of GDLD diagnosed in Saudi Arabia).

2. Methods

2.1. Ethical Approval

The Local Ethical Committee King Saud University, Saudi Arabia, ethically approved the use of tissue procurement. All experiments were done in accordance with the guidelines of “Standing Committee for Research Ethics on Living Creatures (SCRELC)” Saudi Arabia. The policy is available at

2.2. Clinical Details (Figures 1(a)1(d))

A 50-year-old Sudanese patient was referred to King Khalid Specialist Hospital, Riyadh. The patient had been living alone in Riyadh, Saudi Arabia, since 1998. He complained of the sensation of having a foreign body in his eye and reported the gradual decline of vision in both his eyes which developed over many years. He was diagnosed with “typical mulberry-type” GDLD. There was no obvious history of similar ocular conditions in his family.

In August 1997, the patient had penetrating keratoplasty (PKP) in both the right (OD) and left eye (OS). Recurrent amyloid occurred on the PKP cornea. In March 1999, the superficial keratectomy was carried out to the OD, and in January 2005, lamellar keratoplasty (LKP) was carried out to the OS (left eye). The visual acuity in the right eye (OD) was 20/400 and in the left eye (OS) was 20/100 after the last surgery. The intraocular pressure was 18 mmHg in the right eye and 12 mmHg in the left eye.

In May 2011, both eyes presented with multiple superficial corneal nodules of various sizes, the whole cornea was involved including the graft (Figures 1(a) and 1(b)). The left (OS) lamellar corneal graft was still clear. He had mild cataract in both eyes.

In May 2011, the patient had another penetrating keratoplasty to the right eye (OD). Tissue was removed by penetrating keratoplasty of the right eye and was processed for light and electron microscopy. His vision improved without correction. The visual acuity (VA) was OD 20/40 and VA OS 20/50 (Figures 1(c) and 1(d)).

2.3. Genetic Analysis

A blood sample from the patient was sent to Asper Ophthalmics Ltd. for screening against 333 known sequence variants in 13 genes in the corneal dystrophy panel (COL8A, TGFBI, VSX1, CHST6, KRT3, KRT12, GSN, TACSTD2, CYP4V2, SOD1, ZEB1, SLC4A11, and UBIAD1). The mutation in TACSTD2 was further confirmed by sequencing, carried out by Asper Ophthalmics Ltd.

2.4. Light Microscopy and Electron Microscopy

Half of the cornea was fixed in 10% formalin overnight and then washed with phosphate buffer, followed by dehydration in ethanol (70% to 100%). The tissue was embedded in paraffin. Ten micron sections were cut and stained with the standard method of hematoxylin and eosin (H&E). The presence of GDLD was confirmed by classical staining for amyloid with PAS, Congo red, and polarizing Congo red.

For electron microscopy, half of the cornea was fixed in 2.5% glutaraldehyde containing 0.05% Cuprolinic blue in sodium acetate and magnesium chloride. The tissue was dehydrated in ethanol (70% to 100%) and embedded in Spurr resin at 70°C for 8 hrs [13]. Ultrathin sections were cut with RMC ultracut microtome and stained with uranyl acetate and lead citrate. The sections were observed under transmission electron microscope JOEL 1400. The digital images were taken with a bottom mounted Quamesa CCD camera.

3. Results

3.1. Genetic Analysis of GDLD Cornea

Our genetic analysis has shown that a homozygous c.355T > A mutation (rs80358227) in exon 1 of the TACSTD2 (M1S1) gene was present in our GDLA patient. As a result of this mutation, a pathogenic amino acid alteration (p.Cysl19Ser in NCBI entry NP_002344.2) had occurred (Table 1). This mutation has been reported previously in two families of Tunisian origin [14].

Sample IDGeneExonNucleotide changeAmino acid changeGenotype resultsZygosityType of variationVerified sequence

MaleTACSTD2Ex1c.355T > Ap.Cys119SerA/THOMMut+

SNP: single nucleotide polymorphism, HOM: homozygous, HET: heterozygous, and Mut: mutation.
3.2. Histopathological Observation of GDLD Cornea

In the GDLD cornea, the epithelium was very thick and had degenerated (Figures 2(a) and 2(b)). The aggregates of amyloid fibrils were present below the epithelial region and in various parts of the stroma. In some parts, the epithelium was elevated and thin due to the accumulation of the amyloid deposits (Figures 2(a) and 2(b)). Keratocytes had also degenerated. The deposits were Congo red- and PAS-positive and showed apple-green birefringence under polarized light (Figures 2(b)2(d)).

3.3. Electron Microscopy of GDLD Cornea

The epithelium contained numerous electron-dense vacuoles and apoptotic nuclei (Figures 3(a) and 3(b)). Most of the tight junctions had degenerated and appeared as electron-lucent vacuoles. There were some normal tight junctions with electron-dense material around them (Figures 3(a) and 3(b)). A thick band of amyloid deposits were present in the subepithelial region (Figure 3(b)), and these deposits consisted of very thin amyloid microfibrils running randomly (Figures 3(c) and 3(d)). Most parts of the epithelium had detached from the basement membrane and BW due to subepithelial growth of the amyloid deposits. In some places the amyloid microfibrils were closely attached to the surface of Bowman’s layer (Figure 3(c)). Bowman’s layer was thick and contained very long collagen fibrils and large deposits of amyloid fibrils (Figure 3(c)). These amyloid fibrils were densely merged with each other (Figure 3(d)).

The deposits of the amyloid fibrils were also observed in between the lamellae of the anterior stroma creating large lucent spaces and vacuoles (Figures 3(e) and 3(f)). The amyloid fibrils were also present within the lamella replacing the collagen fibrils and creating electron-lucent vacuoles (Figures 3(e) and 3(f)). In some parts of the stroma, the deposits of amyloid fibrils were whorl-like structures showing the emergence of the amyloid fibrils from the center of the whorl (Figures 4(a) and 4(b)). These whorl-like structures had electron-dense and electron-lucent areas (Figures 4(a) and 4(b)). The uniform distribution of the collagen fibrils had been disturbed, and collagen fibrils were of variable diameters (Figure 4(c)). The proteoglycans were very large and randomly distributed in between the longitudinally running collagen fibrils (Figures 4(d) and 4(e)). The keratocytes had degenerated and surrounded the amyloid fibrils (Figure 4(f)).

4. Discussion

Our present studies revealed that the gelatinous drop-like deposits in the cornea of a Sudanese patient (50-year-old) living in Saudi Arabia was caused by the occurrence of a homozygous c.355T > A mutation in exon 1 of the TACSTD2 (M1S1) gene. It has been predicted that the mutation in the gene causes pathogenic amino acid changes (Cl19S) in the thyroglobulin-like repeat region. Ren et al. [14] identified the same c.335T > A mutation in two families of Tunisian origin.

In our patient, the epithelium was full of electron-lucent spaces instead of tight junctions. We believed that the degenerated tight junctions coalesced to each other forming electron-lucent spaces (Figures 3(a) and 3(b)). The deposits in our patient were present below the epithelium and in the anterior stroma and showed apple-green birefringence under polarized light. These deposits were positive to Congo red and PAS staining. Ultrastructural studies showed that these deposits had a whorl-like structure in the stroma containing very thin electron-dense and electron-lucent amyloid fibrils. The lamellae of the stroma were spars and degenerated due to the presence of the deposits between the lamellae. The deposits were also present within the lamellae causing degeneration of the collagen fibrils and proteoglycans.

Nakaizumi [1] for the first time reported that GDLD is an autosomal recessive disease and occurs rarely. The important characteristic feature of the disease is the aggregation of the amyloid deposits at the subepithelial region of the cornea bilaterally. There are several other diseases such as Avellino corneal dystrophy (ACD) and lattice corneal dystrophy (LCD) which are caused by the aggregation of the amyloid fibrils. GDLD has been classified into 4 types: (1) band keratopathy, (2) stromal opacity, (3) kumquat-like, and (4) typical mulberry [2, 15]. According to the classification, our patient had “typical mulberry-type” GDLD. It has been reported that the clinical symptoms of GDLD appear as nodular deposits in the central part of the cornea in the first decade of life. In the later stages of life, these deposits increase in number and coalesce to produce a whitish-yellow mulberry appearance [9, 10].

The presence of amyloid deposits below the epithelial region and anterior stroma of a GDLD cornea have been reported by previous authors [3, 9]. Akhtar et al. [13] reported that the epithelium contained apoptotic nucleus and the BW was replaced by pannus connective tissue. The authors reported that the cause of the disease was the mutation in gene M1S1, in which substitution of aspartic acid to alanine had occurred [13]. In our patient, most parts of the epithelium were destroyed due to the development of amyloid deposits and the thickening of the BW. Similar to these previous observations [13], we also found the stromal collagen fibrils were sparse, degenerated, and disorganized, and the proteoglycans were large in between them. Very fine amyloid microfibrils were observed throughout the stroma and BW.

Tsujikawa et al. [16] suggested that the GDLD in Japanese families is caused by the mutation in the M1S1 (alias TROP-2) gene. Calabrese et al. [17] revised the location of the M1S1 in the gene nomenclature and renamed it as a tumor-associated calcium signal transducer 2 (TACSTD2) gene. The mutations in the tumor-associated calcium signal transducer 2 (TACSTD2) gene are located on chromosome 1 (ip32) which leads to the development of the GDLD disorder [3, 16]. In patients suffering with GDLD, 24 mutations have occurred in the TACSTD2 gene [3, 9, 18, 19]. The genetic heterogeneity of the GDLD was also reported when three mutations in the TACSTD2 were not found [6, 9, 13, 14]. A founder effect has been reported for GDLD-causing mutations in Iran and Japan identified Q118X mutations in TACSTD2 in 4 separate families from Japan [9, 16]. Investigation of additional genetic markers in the region confirmed a founder effect, despite extensive phenotypic variability that included family members who suffered from atypical amyloidosis not initially diagnosed as GDLD. Also, as mentioned above, in a study of 13 unrelated families from Iran diagnosed with GDLD, Alavi et al. [9] detected an E227K mutation in TACSTD2 in 10 patients, also finding evidence of a founder effect for this variant.

The TACSTD2 gene product is a multimodule transmembrane glycoprotein of 323 amino acids. It is 2.07 kB in length and has one exon encoding the tumor-associated antigen. This protein is a monomeric cell surface glycoprotein expressed in the cornea, trophoblast, and most carcinomas [3, 20]. The TACSTD2 protein plays an important role as an adhesion receptor between cancer cells and as a calcium signal transducer [9, 18, 21]. It is believed that, in the GDLD cornea, the abnormal secretion of the TACSTD2 protein causes a high permeability or perforation in the epithelium of GDLD that leads to the formation of amyloid deposits and pathogenicity of the disease [9, 11, 22].

Recently, Nakatukasa et al. [23] reported the direct binding of the TACSTD2 protein to CLDN1 (claudin protein) and CLDN7 proteins which protects them from degradation by the ubiquitin-proteasome system [24]. Claudin plays an important role in the formation of tight junctions between the epithelial cells through calcium-independent cell-adhesion activity. The tight junctions define the border between the apical and basolateral compartments of the epithelial cells and control the lateral diffusion of the lipids and proteins between the cells [25].

In our patient, a homozygous c.355T > A mutation in exon 1 of the TACSTD2 (M1S1) gene caused a lack of functional TACSTD2 protein. Perhaps due to the absence of the TACSTD2 protein, loss of tight junction integrity may have caused the formation of large vacuoles which led to the increased permeability of the corneal epithelium, ultimately leading to the subepithelial and stromal deposition of amyloid in the cornea. These amyloid deposits caused degeneration of the collagen fibrils and proteoglycans leading to corneal opacity.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The received funding did not lead to any conflicts of interest regarding the publication of this manuscript.


This work was supported by the Deanship of Scientific Research at King Saud University for funding this research (Grant no. RGP-VPP-219).


  1. G. Nakaizumi, “A rare case of corneal dystrophy,” Acta Society of Ophthalmology of Japan, vol. 18, pp. 949-950, 1914. View at: Google Scholar
  2. T. Ide, K. Nishida, N. Maeda et al., “A spectrum of clinical manifestations of gelatinous drop-like corneal dystrophy in Japan,” American Journal of Ophthalmology, vol. 137, no. 6, pp. 1081–1084, 2004. View at: Publisher Site | Google Scholar
  3. P. Paliwal, J. Gupta, R. Tandon et al., “Identification and characterization of a novel TACSTD2 mutation in gelatinous drop-like corneal dystrophy,” Molecular vision, vol. 16, pp. 729–739, 2010. View at: Google Scholar
  4. H. Kaza, M. R. Barik, M. M. Reddy, R. Mittal, and S. Das, “Gelatinous drop-like corneal dystrophy: a review,” British Journal of Ophthalmology, vol. 101, no. 1, pp. 10–15, 2017. View at: Publisher Site | Google Scholar
  5. H. Kawano, K. Fujiki, A. Kanai, and A. Nakajima, “Prevalence of gelatinous drop-like corneal dystrophy in Japan,” Atarashii Ganka, vol. 9, pp. 1879–1882, 1992. View at: Google Scholar
  6. K. Fujiki, K. Nakayasu, and A. Kanai, “Corneal dystrophies in Japan,” Journal of Human Genetics, vol. 46, no. 8, pp. 431–435, 2001. View at: Publisher Site | Google Scholar
  7. H. Pandrowala, A. Bansal, G. K. Vemuganti, and G. N. Rao, “Frequency, distribution, and outcome of keratoplasty for corneal dystrophies at a tertiary eye care center in South India,” Cornea, vol. 23, no. 6, pp. 541–546, 2004. View at: Publisher Site | Google Scholar
  8. A. Markoff, N. Bogdanova, C. E. Uhliq, M. Groppe, J. Horst, and I. Kennerknecht, “A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy,” Molecular vision, vol. 12, pp. 1473–1476, 2006. View at: Google Scholar
  9. A. Alavi, E. Elahi, M. H. Tehrani et al., “Four mutations (three novel, one founder) inTACSTD2 among Iranian GDLD patients,” Investigative Opthalmology & Visual Science, vol. 48, no. 10, pp. 4490–4497, 2007. View at: Publisher Site | Google Scholar
  10. Y. Ohnishi, Y. Shinoda, T. Ishibashi, and Y. Taniguchi, “The origin of amyloid in gelatinous drop-like corneal dystrophy,” Current Eye Research, vol. 2, no. 4, pp. 225–231, 1982. View at: Publisher Site | Google Scholar
  11. S. Konoshita, K. Nishida, A. Dota et al., “Epithelial barrier function and ultrastructure of gelatinous drop-like corneal dystrophy,” Cornea, vol. 19, no. 4, pp. 551–555, 2000. View at: Google Scholar
  12. E. R. Büchi, B. Daicker, S. Uffer, and F. Gudat, “Primary gelatinous drop-like corneal dystrophy in a white woman: a pathologic, ultrastructural, and immunohistochemical study,” Cornea, vol. 13, no. 2, pp. 190–194, 1994. View at: Publisher Site | Google Scholar
  13. S. Akhtar, A. J. Bron, X. Qin, R. C. Creer, J. A. Guggenheim, and K. M. Meek, “Gelatinous drop-like corneal dystrophy in a child with developmental delay: clinicopathological features and exclusion of the M1S1 gene,” Eye, vol. 19, no. 2, pp. 198–204, 2005. View at: Publisher Site | Google Scholar
  14. Z. Ren, P.-Y. Lin, G. K. Klintworth et al., “Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy,” Human Genetics, vol. 110, no. 6, pp. 568–577, 2002. View at: Publisher Site | Google Scholar
  15. B. Zhang and Y. F. Yao, “Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient,” Molecular Vision, vol. 16, pp. 1570–1575, 2010. View at: Google Scholar
  16. M. Tsujikawa, H. Kurahashi, T. Tanaka et al., “Identification of the gene responsible for gelatinous drop-like corneal dystrophy,” Nature Genetics, vol. 21, no. 4, pp. 420–423, 1999. View at: Publisher Site | Google Scholar
  17. G. Calabrese, C. Crescenzi, E. Morizio, G. Palka, E. Guerra, and S. Alberti, “Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization,” Cytogenetic and Genome Research, vol. 92, no. 1-2, pp. 164-165, 2001. View at: Publisher Site | Google Scholar
  18. E. Ripani, A. Sacchetti, D. Corda, and S. Alberti, “Human Trop-2 is a tumor associated calcium signal transducer,” International Journal of Cancer, vol. 76, pp. 671–676, 1998. View at: Publisher Site | Google Scholar
  19. Y. Jing, C. Liu, and L. Wang, “A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy,” Molecular Vision, vol. 15, pp. 1580–1588, 2009. View at: Google Scholar
  20. R. Stein, A. Basu, S. Chen, L. B. Shih, and D. M. Goldenberg, “Specificity and properties of MAb RS7–3G11 and the antigen defined by this pancarcinoma monoclonal antibody,” International Journal of Cancer, vol. 55, no. 6, pp. 938–946, 1993. View at: Publisher Site | Google Scholar
  21. M. M. Zutter, “Gastrointestinal carcinoma antigen GA733: target for immunodestruction and potential modifier of invasiveness and chemoresponsiveness,” JNCI: Journal of the National Cancer Institute, vol. 90, no. 9, pp. 642–644, 1998. View at: Publisher Site | Google Scholar
  22. S. Kinoshita, N. Yokoi, and A. Komuro, “Barrier function of ocular surface epithelium,” Advances in Corneal Research, vol. 5, no. 47–55, 1997. View at: Publisher Site | Google Scholar
  23. M. Nakatsukasa, S. Kawasaki, K. Yamasaki et al., “Two novel mutations of TACSTD2 found in three Japanese gelatinous drop-like corneal dystrophy families with their aberrant subcellular localization,” Molecular Vision, vol. 17, pp. 965–970, 2011. View at: Google Scholar
  24. M. Nakatsukasa, S. Kawasaki, K. Yamasaki et al., “Tumor-associated calcium signal transducer 2 is required for the proper subcellular localization of claudin 1 and 7: implications in the pathogenesis of gelatinous drop-like corneal dystrophy,” The American journal of pathology, vol. 177, no. 3, pp. 1344–1355, 2010. View at: Publisher Site | Google Scholar
  25. J.-Y. Zheng, D. Yu, M. Foroohar et al., “Regulation of the expression of the prostate-specific antigen by claudin-7,” Journal of Membrane Biology, vol. 194, no. 3, pp. 187–197, 2003. View at: Publisher Site | Google Scholar

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