Frequent somatic reversion of KRT1 mutations in ichthyosis with confetti. - Abstract - Europe PMC
Woman has 'burning' skin which leaves her red and turns eyelids 'inside out' - World News - Mirror Online
ski on X: "9. Ichthyosis en confetti https://t.co/dcA8A4NbhK" / X
JAMA Dermatology on X: "Novel classification of #ichthyosis with confetti as a syndrome @esdrgva http://t.co/Aq16GnFD7r http://t.co/0JxXr6UYkZ" / X
IAMA person with a severe form of ichthyosis, often talked about on r/WTF. Pictures of my skin inside. AMA. : r/IAmA
![PDF] The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3 ′ End of KRT 10 FromDisease to a Syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/2b0e30964d4315dc2c26e44d10fedab455564f0d/4-Figure1-1.png "PDF] The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3 ′ End of KRT 10 FromDisease to a Syndrome | Semantic Scholar")
PDF] The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3 ′ End of KRT 10 FromDisease to a Syndrome | Semantic Scholar
Ocular manifestation of Ichthyosis - ScienceDirect
Ichthyoses, Erythrokeratodermas, and Related Disorders | Plastic Surgery Key
Major and minor clinical features of ichthyosis with confetti.... | Download Scientific Diagram
Mitotic recombination in patients with ichthyosis causes reversion of dominant mutations in KRT10. - Abstract - Europe PMC
Ichthyosis with confetti: MedlinePlus Genetics
Epidermolytic ichthyosis | DermNet
Ichthyosis: En Confetti - Positive Exposure
Ichthyosis with confetti - Wikipedia
I | SpringerLink
Confetti' skin disease spoils the party for bad genes
Ichthyosis (overview) - Altmeyers Encyclopedia - Department Dermatology
IJMS | Free Full-Text | First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses
![PDF] Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/df57d3d36e0bf795aa5f738c0a297409279f4609/4-Figure3-1.png "PDF] Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis. | Semantic Scholar")
PDF] Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis. | Semantic Scholar
Coexistence of mutations in keratin 10 (KRT10) and the mitochondrial genome in a patient with ichthyosis with confetti and Leber's hereditary optic neuropathy - Kalinska‐Bienias - 2017 - American Journal of Medical
Ichthyosis with confetti: clinics, molecular genetics and management | Orphanet Journal of Rare Diseases | Full Text
Ichthyoses, Erythrokeratodermas, and Related Disorders | Plastic Surgery Key
