Pellucid marginal degeneration




Input patient's signs and symptoms


Narrow down the case reports



Total: 45 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(29.4%)
15186210
Pellucid marginal degeneration and scleroderma.
Sii F, Lee GA, Sanfilippo P, Stephensen DC.
Clin Exp Optom. 2004;87(3):180-4.
Keratitis Keratoconjunctivitis sicca
Astigmatism Cornea Corneal Topography Differential Diagnosis Females Homo sapiens Middle Aged Pathological Dilatation Systemic Scleroderma
2
(17.5%)
23943692
(3740469)
Acute Corneal Hydrops following Post-keratoplasty Suture Removal in Pellucid Marginal Degeneration.
Fallahi Motlagh B, Mortazavi SZ.
J Ophthalmic Vis Res. 2013;8(2):172-4.
Corneal scarring
2
(17.5%)
10832988
Keratectasia induced by laser in situ keratomileusis in keratoconus.
Schmitt-Bernard CF, Lesage C, Arnaud B.
J Refract Surg. 2000;16(3):368-70.
Corneal scarring
Cornea Corneal Diseases Corneal Topography Homo sapiens Keratoconus Keratomileusis, Laser In Situ Male Middle Aged Pathological Dilatation Visual Acuity
4
(4.0%)
30729234
Corneal crosslinking in a case with Axenfeld-Rieger syndrome and unilateral pellucid marginal degeneration.
Koc M, Kosekahya P, Inanc M, Tekin K.
Ther Adv Ophthalmol. 2019;11:2515841418822288.
Posterior embryotoxon
4
(4.0%)
29653558
(5899354)
Acute hydrops with a 180-degree massive edematous cavern demonstrated by three dimensional view of anterior segment optical coherence tomography in a patient with pellucid marginal corneal degeneration, a case report.
Winegarner A, Oie Y, Nishida K.
BMC Ophthalmol. 2018;18(1):92.
Visual loss
Adult Corneal Diseases Females Homo sapiens Tomography, Optical Coherence
4
(4.0%)
27994396
(5141626)
Surgical Treatment of Corneal Ectasia with Motowa's Trephine and Selective Suturing Technique.
Al-Motowa S, Al-Harby M.
Middle East Afr J Ophthalmol. 2016;23(4):315-317.
Astigmatism
Adult Cornea Corneal Topography Homo sapiens Male Ophthalmologic Surgical Procedures Pathological Dilatation Suture Techniques Visual Acuity
4
(4.0%)
27146937
(4869465)
Corneal perforation during scleral indentation in a patient with pellucid marginal degeneration.
Mercieca K, Dharmasena A, Hopley C.
Indian J Ophthalmol. 2016;64(3):233-4.
Corneal perforation
Adult Cornea Corneal Perforation Corneal Topography Females Homo sapiens Sclera Visual Acuity
4
(4.0%)
23635856
Direct surgical repair of corneal perforation in pellucid marginal degeneration: a case series.
Chan E, Snibson GR, Poon A.
Cornea. 2013;32(7):1058-62.
Corneal perforation
Adult Corneal Diseases Corneal Perforation Corneal Topography Females Homo sapiens Keratoplasty, Penetrating Male Middle Aged Pathological Dilatation Suture Techniques Viscosupplements Visual Acuity
4
(4.0%)
23571261
(4061688)
Collagen cross-linking in the treatment of pellucid marginal degeneration.
Hassan Z, Nemeth G, Modis L, Szalai E, Berta A.
Indian J Ophthalmol. 2014;62(3):367-70.
Irregular astigmatism
Corneal Stroma Corneal Topography Cross-Linking Reagents Homo sapiens Male Middle Aged Photochemotherapy Photosensitizing Agents Visual Acuity
4
(4.0%)
23198069
(3498565)
Spontaneous corneal hydrops and perforation in pellucid marginal degeneration; a case report.
Gharebaghi D, Fallahi B, Javadzadeh A, Amiraslanzadeh G.
J Ophthalmic Vis Res. 2009;4(3):174-6.
Corneal perforation
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 13

HPO ID Term # of case reports
HP:0100583 Corneal perforation 7
HP:0000563 Keratoconus 6
HP:0031792 Irregular astigmatism 4
HP:0000483 Astigmatism 2
HP:0000545 Myopia 2
HP:0001119 Keratoglobus 2
HP:0000505 Visual impairment 1
HP:0000518 Cataract 1
HP:0000969 Edema 1
HP:0011003 High myopia 1
HP:0012804 Corneal ulceration 1
HP:0031789 Against the rule astigmatism 1
HP:0500041 Myopic astigmatism 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID