Disease: Dyschromatosis universalis hereditaria
- A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
- A Case of Sporadic Dyschromatosis Universalis Hereditaria
- A Case Report of Dyschromatosis Universalis Hereditaria (DUH) with Primary Ovarian Failure (POF)
- A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family
- A novel P53/POMC/Gαs/SASH1 autoregulatory feedback loop activates mutated SASH1 to cause pathologic hyperpigmentation
- A Rare Case of Foveal Hypoplasia With Dyschromatosis Universalis
- ABCB6 Resides in Melanosomes and Regulates Early Steps of Melanogenesis Required for PMEL Amyloid Matrix Formation
- Abrupt onset of dyschromatosis universalis hereditaria with macromelanosomes
- An Algorithmic Approach Towards Diagnosis of Patients with Hereditary Reticulate Pigmentary Disorders- A narrative review
- Atypical cases of Dowling-Degos disease
- Atypical presentation of dyschromatosis universalis hereditaria with a novel ABCB6 mutation
- Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders
- Dermoscopic patterns of dyschromatosis universalis hereditaria with acral involvement
- Differential Diagnosis of Two Chinese Families with Dyschromatoses by Targeted Gene Sequencing
- Dowling-Degos disease
- Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family
- Dyschromatosis
- Dyschromatosis universalis hereditaria
- Dyschromatosis universalis hereditaria
- Dyschromatosis Universalis Hereditaria
- Dyschromatosis universalis hereditaria
- Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family
- Dyschromatosis universalis hereditaria in a young Nigerian female
- Dyschromatosis universalis hereditaria in an African American male
- Dyschromatosis Universalis Hereditaria with Hypospadias: A Rare Association
- Dyschromatosis universalis hereditaria with involvement of palms
- Dyschromatosis Universalis Hereditaria with Oral Leukokeratosis--A Case of Mistaken Identity and Review of the Literature
- Dyschromatosis universalis hereditaria with renal failure
- Dyschromatosis universalis hereditaria: a case report
- Dyschromatosis universalis hereditaria: a case report
- Dyschromatosis universalis hereditaria: a rare entity
- Dyschromatosis universalis hereditaria: a unique disorder
- Dyschromatosis universalis hereditaria: an electron microscopic examination
- Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23
- Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation
- Dyschromatosis universalis hereditaria: Infrequent genodermatoses in India
- Dyschromatosis universalis hereditaria: report of a case
- Dyschromatosis universalis hereditaria: report of a case and review of the literature
- Dyschromatosis universalis hereditaria: report of six cases from a family
- Dyschromatosis universalis hereditaria: two cases
- Dyschromatosis universalis hereditaria: two cases in a Chinese family
- Dyschromatosis universalis hereditaria. An unusually rare clinical picture
- Dyschromatosis Unwersalis Hereditaria
- Dyschromias: A Series of Five Interesting Cases from India
- Effects of idebenone on color vision in patients with leber hereditary optic neuropathy
- ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis
- Generalized Dowling-Degos disease
- Generalized reticulated hyperpigmented patches interspersed with hypopigmented macules
- Genetical studies on skin diseases. VII. Dyschromatosis universalis hereditaria in 5 generations
- Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria
- Hereditary pigmentary disorders: light from the East
- Identification of a Novel Mutation in <em>SASH1</em> Gene in a Chinese Family With Dyschromatosis Universalis Hereditaria and Genotype-Phenotype Correlation Analysis
- Identification of a Novel Mutation in SASH1 Gene in a Chinese Family With Dyschromatosis Universalis Hereditaria and Genotype-Phenotype Correlation Analysis
- Inherited Reticulate Pigmentary Disorders
- KITLG mutations cause familial progressive hyper- and hypopigmentation
- Localized form of dyschromatosis universalis hereditaria in a 14-year-old girl
- Mutated SASH1 promotes Mitf expression in a heterozygous mutated SASH1 knock‑in mouse model
- Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis
- Mutations in ABCB6 cause dyschromatosis universalis hereditaria
- Novel missense mutation of SASH1 in a Chinese family with dyschromatosis universalis hereditaria
- Novel missense mutations of ABCB6 in two chinese families with dyschromatosis universalis hereditaria
- Novel mutations in <em>SASH1</em> associated with dyschromatosis universalis hereditaria
- Novel mutations in SASH1 associated with dyschromatosis universalis hereditaria
- Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria
- p53 regulates ERK1/2/CREB cascade via a novel SASH1/MAP2K2 crosstalk to induce hyperpigmentation
- Photoletter to the editor: Dyschromatosis universalis hereditaria: an infrequently occurring entity in Europe
- Removal of facial and labial lentigines in dyschromatosis universalis hereditaria with a Q-switched alexandrite laser
- Removal of forearm lentigines in dyschromatosis universalis hereditaria with a 755-nm Q-switched alexandrite laser
- Retyping and molecular pathology diagnosis of dyschromatosis universalis hereditaria
- SASH1 promotes melanin synthesis and migration via suppression of TGF-β1 secretion in melanocytes resulting in pathologic hyperpigmentation
- Sporadic Dyschromatosis Universalis Hereditaria: A Second Case Report From Iran
- The PER3(rs772027021) SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- The PER3<sup>rs772027021</sup> SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Thrombocytopenia in dyschromatosis universalis hereditaria
- Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria
- Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria
- Two Taiwanese siblings with dyschromatosis universalis hereditaria
- Ultrastructural Investigations in an Autosomal Recessively Inherited Case of Dyschromatosis Universalis Hereditaria
- Uncovering a new SASH1 mutation associated with dyschromatosis universalis hereditaria using whole-exome-sequencing: A case report
- Updated review of genetic reticulate pigmentary disorders