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Last Updated: 10/31/2025
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Found 88 publications
Dyschromatosis universalis hereditaria: Dermoscopic insights in a patient with intellectual disability.
Journal: JAAD case reports
Published: October 13, 2025
SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature.
Journal: Pigment cell & melanoma research
Published: April 26, 2025
Dyschromatosis universalis hereditaria with SASH1 mutation improved with picosecond laser treatment.
Dyschromatosis universalis hereditaria with SASH1 mutation improved with picosecond laser treatment.
Journal: Skin health and disease
Published: March 05, 2025
Dermatological Enigma Unveiled: A Rare Case Report on Dowling-Degos Disease.
Journal: International journal of applied & basic medical research
Published: April 10, 2024
Case report: Clinicopathological characteristics of SASH1 mutation-related dyschromatosis: a rethinking of the classification of dyschromatosis.
Journal: Frontiers in genetics
Published: April 08, 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
Last Updated: 10/31/2025