Results 71 to 80 of about 434 (146)

Analysis of genotype/phenotype correlations in Japanese patients with dyschromatosis symmetrica hereditaria

Dyschromatosis symmetrica hereditaria (DSH) is one of the genetic pigmentation disorders and shows characteristic mixture of hyper- and hypo-pigmented small macules on the extremities. Heterozygous mutations in the adenosine deaminase acting on RNA1 gene
Kobayashi, Tomoko, Kono, Michihiro, Tsutsui, Kiyohiro, Takeichi, Takuya, Takai, Ayaka, Suganuma, Mutsumi, Akita, Hirotaka, Inasaka, Yu, Muro, Yoshinao, Akiyama, Masashi   +9 more
core  

Hyper- and Hypo-pigmented Small Macules on Face, Neck and Extremities: A Quiz. [PDF]

Acta Derm Venereol, 2023
Zhang J, Lai Y, Shi Z.
europepmc   +1 more source

Dyschromatosis Symmetrica Hereditaria

Nishi Nihon Hifuka, 1973
openaire   +1 more source

<i>Adar</i>-associated Aicardi Goutières syndrome in a child with bilateral striatal necrosis and recurrent episodes of transaminitis. [PDF]

BMJ Case Rep, 2023
van Toorn R, van Niekerk M, Moosa S, Goussard P, Solomons R.   +4 more
europepmc   +1 more source

Dermoscopic and Onychoscopic Features of Dyskeratosis Congenita. [PDF]

Indian Dermatol Online J, 2022
Vasani R, Baddireddy K.
europepmc   +1 more source

A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family. [PDF]

JAAD Case Rep, 2022
Aldokhayel S, Nouf A, Khalid A, Faisal A, Maram A, Ahmed A, Fahad A.   +6 more
europepmc   +1 more source

Sporadic Dyschromatosis Universalis Hereditaria: A Second Case Report From Iran. [PDF]

Cureus, 2021
Dogohar S, Alirezaei P, Ghasemi Basir H, Jamshidi M, Etaee F.   +4 more
europepmc   +1 more source

A novel deletion mutation in the adenosine deaminase RNA-specific gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria

Dermatologica Sinica, 2011
Yi-An Chen, Sheau-Chiou Chao, Julia Yu-Yun Lee   +2 more
doaj   +1 more source

Follicular Dowling-Degos Disease Camouflaged as Comedones: A Case Report and Literature Review. [PDF]

Cureus, 2022
S A, Rajagopal P, Gopinath H, Rupa Ramani J.   +3 more
europepmc   +1 more source

Chronic arsenicosis. [PDF]

BMJ Case Rep, 2021
Bhanja DB, Sil A, Sen SS, Chandra A.
europepmc   +1 more source