نتایج جستجو برای: hypopigmentation

تعداد نتایج: 865  

Journal: :Contact dermatitis 2010
Murugusundram Sundaram

1941
S. B. Das Gupta

Journal: :Investigative ophthalmology & visual science 2017
Ryoko Oki Kisaburo Yamada Satoko Nakano Kenichi Kimoto Ken Yamamoto Hiroyuki Kondo Toshiaki Kubota

Purpose We report the clinical characteristics of a Japanese family with autosomal dominant oculocutaneous albinism and a SLC45A2 gene mutation. Methods A total of 16 members of a Japanese family with general hypopigmentation and foveal hypoplasia underwent detailed clinical examinations. We evaluated the severity of foveal hypoplasia using spectral-domain optical coherence tomography (SD-OCT...

Journal: :Clinical and experimental dermatology 2008
J Mashiah S Brenner

The pathogenesis of vitiligo was examined for clues to the pigmentary changes that may occur after treatment with topical imiquimod. The literature varies on the pigmentary changes induced by topical use of imiquimod. The US Food and Drugs Administration lists 68 reports of pigmentary changes out of a total of 1257 reports related to imiquimod lodged from 1997 to 2003. Some studies describe vit...

2014
Genji Imokawa Koichi Ishida

Few anti-pigmenting agents have been designed and developed according to their known hyperpigmentation mechanisms and corresponding intracellular signaling cascades. Most anti-pigmenting agents developed so far are mechanistically involved in the interruption of constitutional melanogenic mechanisms by which skin color is maintained at a normal and unstimulated level. Thus, owing to the difficu...

Journal: :Mechanisms of Development 2006
Ramin Mollaaghababa Hakami Ling Hou Laura L. Baxter Stacie K. Loftus E. Michelle Southard-Smith Arturo Incao Jun Cheng William J. Pavan

Mutations in the transcription factor Sox10 or Endothelin Receptor B (Ednrb) result in Waardenburg Syndrome Type IV (WS-IV), which presents with deficiencies of neural crest derived melanocytes (hypopigmentation) and enteric ganglia (hypoganglionosis). As Sox10 and Ednrb are expressed in mouse migratory neural crest cells and melanoblasts, we investigated the possibility that SOX10 and EDNRB fu...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Amanda L Blasius Katharina Brandl Karine Crozat Yu Xia Kevin Khovananth Philippe Krebs Nora G Smart Antonella Zampolli Zaverio M Ruggeri Bruce A Beutler

The classical recessive coat color mutation misty (m) arose spontaneously on the DBA/J background and causes generalized hypopigmentation and localized white-spotting in mice, with a lack of pigment on the belly, tail tip, and paws. Here we describe moonlight (mnlt), a second hypopigmentation and white-spotting mutation identified on the C57BL/6J background, which yields a phenotypic copy of m/...

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