Heredity and in vivo confocal microscopy of punctiform and polychromatic pre-Descemet dystrophy

Purpose To describe and analyze the biomicroscopic features and in vivo confocal microscopy of the crystalline form of pre-Descemet corneal dystrophy (PDCD). Methods We examined two non-related families using biomicroscopy, in vivo confocal microscopy, and a genetic study using a gene panel test, lo...

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Bibliographic Details
Published in:Graefe's archive for clinical and experimental ophthalmology 2018-09, Vol.256 (9), p.1661-1667
Main Authors: Recine, María Angélica Henríquez, Lima, Kelly Sonia Marquina, García, Elena Vallespín, García-Miñaur, Sixto, Del Castillo, José Manuel Benitez, de los Bueis, Ana Boto
Format: Article
Language:English
Subjects:
Adult
Aged
Autosomal dominant inheritance
Child
Cornea
Corneal Dystrophies, Hereditary - diagnosis
Corneal Dystrophies, Hereditary - genetics
Corneal Dystrophies, Hereditary - metabolism
Corneal Stroma - pathology
Descemet Membrane - pathology
DNA - genetics
DNA Mutational Analysis
Female
Heredity
Humans
Male
Medicine
Medicine & Public Health
Microscopy, Confocal - methods
Middle Aged
Mutation
Ophthalmology
Pedigree
Phosphatidylinositol 3-Kinases - genetics
Phosphatidylinositol 3-Kinases - metabolism
Young Adult
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Summary:Purpose To describe and analyze the biomicroscopic features and in vivo confocal microscopy of the crystalline form of pre-Descemet corneal dystrophy (PDCD). Methods We examined two non-related families using biomicroscopy, in vivo confocal microscopy, and a genetic study using a gene panel test, looking for mutations in the PIKFYVE gene. Results A slit-lamp examination of the first family revealed polychromatic crystalline punctiform opacities distributed all over the stroma in 8 of 11 family members in three generations with an autosomal dominant inheritance. The second family showed in three of four members in two generations the same opacities located in the pre-Descemet region. It was also a hint for autosomal dominant inheritance. The in vivo confocal microscopy identified numerous rounded and hyperreflective stromal particles measuring 10–15 μm in diameter, with the highest density in the posterior stroma and with normal keratocytes. No systemic disease was diagnosed. No variants or mutations were identified in PIKFYVE gene. Conclusions Polychromatic deposits in patients with Punctiform and Polychromatic Pre-Descemet corneal dystrophy can be located not only in the deep stroma but also in the anterior and middle stroma. Our presentation reveals the possibility of considering this characteristic corneal disorder as a corneal dystrophy of its own and not as a subtype of pre-Descemet corneal dystrophy.
ISSN:0721-832X
1435-702X
DOI:10.1007/s00417-018-3993-x