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Last Updated: 03/06/2025
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Found 84 publications
Dermatological Enigma Unveiled: A Rare Case Report on Dowling-Degos Disease.
Journal: International journal of applied & basic medical research
Published: April 10, 2024
Uncovering a new SASH1 mutation associated with dyschromatosis universalis hereditaria using whole-exome-sequencing: A case report.
Journal: Medicine
Published: August 06, 2023
An algorithmic approach towards diagnosis of patients with hereditary reticulate pigmentary disorders: a narrative review.
Journal: Clinical and experimental dermatology
Published: May 12, 2023
Dyschromatosis universalis hereditaria.
Journal: International journal of dermatology
Published: April 27, 2023
The role of ATP-binding Cassette subfamily B member 6 in the inner ear.
Journal: Nature communications
Published: March 14, 2023
Retyping and molecular pathology diagnosis of dyschromatosis universalis hereditaria.
Journal: Experimental dermatology
Published: March 03, 2023
Dermoscopic patterns of dyschromatosis universalis hereditaria with acral involvement.
Journal: Clinical and experimental dermatology
Published: January 20, 2023
The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria.
Journal: Journal of molecular medicine (Berlin, Germany)
Published: August 17, 2022
A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family.
Journal: JAAD case reports
Published: January 13, 2022
Dyschromatosis Universalis Hereditaria.
Journal: Kathmandu University medical journal (KUMJ)
Published: November 23, 2021
Last Updated: 03/06/2025