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119 Possible Causes for Prominent Schwalbe Line

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  • Familial Isolated Trichomegaly

    Patients with Hermansky-Pudlak syndrome have various anterior segment abnormalities that include the following: a prominent Schwalbe line, iris transillumination, and presenile[emedicine.medscape.com] Schwalbe line, iris transillumination, foveal hypoplasia, and albinotic retinal mid periphery, as shown in the image below. [32] Photo showing light brown eyes and a red[emedicine.medscape.com] […] syndrome Ocular findings in Hermansky-Pudlak syndrome include poor visual acuity, refractive errors associated with with-the-rule astigmatism, strabismus, congenital nystagmus, prominent[emedicine.medscape.com]

  • Axenfeld-Rieger Syndrome Type 3

    Features include posterior corneal embryotoxon, prominent Schwalbe line and iris adhesion to the Schwalbe line, hypertelorism, hypodontia, sensorineural deafness, redundant[uniprot.org] The most prominent eye defects in ARS include (1) Axenfeld anomaly, characterized by a prominent Schwalbe’s line and adherence of the iris to the cornea and trabecular meshwork[genedx.com] Gonioscopically, the features were similar in both the eyes and included a prominent anteriorly shifted Schwalbe's line with prominent iridocorneal tissue strands, anterior[ijo.in]

  • De Hauwere Syndrome

    Schwalbe's line , an opaque ring around the cornea known as posterior embryotoxon, and hypoplasia of the iris can occur.[research.omicsgroup.org] Glaucoma develops during adolescence or late-childhood, but often occurs in infancy. [5] [9] In addition, a prominent Schwalbe's line , an opaque ring around the cornea known[ipfs.io] Glaucoma develops during adolescence or late childhood, but often occurs in infancy. [8] [9] In addition, a prominent Schwalbe's line , an opaque ring around the cornea known[en.wikipedia.org]

  • RAPADILINO Syndrome

    Schwalbe's lines, absence of mesodermal layer of iris, tilted optic discs, tempo-retinal degeneration, pigment deposits over cornea and conjunctiva), skeletal abnormalities[ijdvl.com] […] features include short stature, sparse scalp hair, sparse/absent eyelashes and/or eyebrows, ophthalmic abnormalities (juvenile cataract, keratoconus, exophthalmos, glaucoma, prominent[ijdvl.com]

  • Axenfeld Syndrome

    RESULTS The patient had prominent Schwalbe's line in all quadrants, iris atrophy, and secondary glaucoma in both eyes.[unboundmedicine.com] […] bridging the angle from the peripheral iris to the prominent Schwalbe's line). [2] Nearly 50% of the subjects present with secondary glaucoma. [2] In A-R syndrome, Schwalbe's[ijo.in] Features include posterior corneal embryotoxon, prominent Schwalbe line and iris adhesion to the Schwalbe line, hypertelorism, hypodontia, sensorineural deafness, redundant[uniprot.org]

  • Goniodysgenesis

    Schwalbe's line, the membranes were vascularized and their appearance changed over time.[ncbi.nlm.nih.gov] Schwalbe line * Iris adhesions * Eye abnormality * Premature birth * Infant feeding problems * Respiratory distress * Tricuspid valve anomaly * Absent iris Causes - Goniodysgenesis[checkorphan.org] Schwalbe’s line.[healio.com]

  • Blepharophimosis-Epicanthus Inversus-Ptosis Syndrome

    Gonioscopically, the features were similar in both the eyes and included a prominent anteriorly shifted Schwalbe's line with prominent iridocorneal tissue strands, anterior[ijo.in] Figure 2: Goniophotograph showing a prominent Schwalbe's line with peripheral broad based anterior synechiae and iris hole Click here to view Discussion Since its original[ijo.in] […] anteriorly displaced Schwalbe's line, iridocorneal tissue strands with high insertion of iris into the posterior trabecular meshwork, iris abnormalities including corectopia[ijo.in]

  • Iridocorneal Endothelial Syndrome

    line.[ncbi.nlm.nih.gov] This primordial endothelium also produces excessive and atypical basement membrane, especially near the corneolimbal junction, which accounts for the prominent Schwalbe's[ncbi.nlm.nih.gov]

  • Sclerocornea

    , anteriorly displaced Schwalbe's line at the corneal limbus or edge), retinal vascular tortuosity, eyelid hooding, strabismus, and astigmatism.[ncbi.nlm.nih.gov] 22q11.2 deletion syndrome (which encompasses the phenotypes of DiGeorge, velocardiofacial, and Takao (conotruncal-anomaly-face) syndromes) have included posterior embryotoxon (prominent[ncbi.nlm.nih.gov]

  • Crandall Syndrome

    AXENFELD-RIEGER SPECTRUM Characteristics and Genetics The Axenfeld-Rieger spectrum (ARS) is characterized by an anteriorly displaced, prominent Schwalbe line (posterior embryotoxon[glaucomatoday.com]

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