Results 91 to 100 of about 1,435 (174)

Piebaldismo en un recién nacido. Leucodermia rara Piebaldism in a newborn child. A rare leukoderma

Revista de Ciencias Médicas de Pinar del Río, 2013
El piebaldismo es un defecto genético infrecuente donde las anomalías en la pigmentación de la piel se restringen al pelo y a la piel, aunque se han hallado ciertas similitudes con fenotipos de otras enfermedades.
Noemí Bárbara Cabrera Domínguez, Gloria Breto Rodríguez, Marelis Castro Márquez, Mirka Rosa Torres, Rita Inés Milián Casanova   +4 more
doaj  

Molecular Basis of Human Piebaldism

Journal of Investigative Dermatology, 1994
Piebaldism is an autosomal dominant genetic disorder of pigmentation characterized by congenital patches of white skin and hair that lack melanocytes. Piebaldism results from mutations of the KIT proto-oncogene, which encodes the cell-surface receptor transmembrane tyrosine kinase for an embryonic growth factor, Steel factor.
openaire   +2 more sources

Abstract

JPGN Reports, Volume 6, Issue S2, Page S1-S814, September 2025.
wiley   +1 more source

Sustained Repigmentation in Vitiligo and Leukodermas Using Melanocyte–Keratinocyte Transplantation: 7 Years of Data

Clinical, Cosmetic and Investigational Dermatology
Nuttaporn Nuntawisuttiwong,* Punyanut Yothachai,* Teerapat Paringkarn, Chayada Chaiyabutr, Chanisada Wongpraparut, Narumol Silpa-archa Department of Dermatology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand&ast ...
Nuntawisuttiwong N, Yothachai P, Paringkarn T, Chaiyabutr C, Wongpraparut C, Silpa-archa N   +5 more
doaj  

Ultrastructural studies distinguish skin diversities among Galápagos iguanas

Biology Direct
Iguanas exhibit diverse colors and behaviors reflecting evolutionarily adaptation to various habitats; in particular, the Galápagos iguanas represent unique color morphologies with distinct ecological niches.
Manuel Scimeca, Rita Bonfiglio, Giuliano Colosimo, Eleonora Candi, Glenn P. Gerber, Gregory A. Lewbart, Alessandro Mauriello, Gerry Melino, Christian Sevilla, Yufang Shi, Ying Wang, Gabriele Gentile   +11 more
doaj   +1 more source

Diagnosing congenital hypochromic patches. [PDF]

BMJ Case Rep, 2023
De Brito Garcia Sousa Ferro I, Girbal I, Lopes M.   +2 more
europepmc   +1 more source

Distribution record of a xanthic Zambezi Flap-shelled Terrapin Cycloderma frenatum at the Rufiji River, Tanzania [PDF]

, 2016
This paper reports the discovery of the Zambezi Flap-shelled Terrapin Cycloderma frenatum in the Selous Game Reserve along the Rufiji River, Tanzania.
Jubber, Walter R, Leyendecker, Martin
core   +1 more source

Piebaldism with café-au-lait macules resulting from a novel mutation of KIT gene in a three-generation Chinese family. [PDF]

Skin Res Technol, 2023
Li X, Xing X, Liang X, Song C, Yang J, Ren D, Zhou Y.   +6 more
europepmc   +1 more source

A piebald family.

Indian journal of dermatology, venereology and leprology, 2012
Piebaldism is an uncommon congenital hypomelanotic disorder characterized by a white forelock and vitiligo like amelanotic macules. We report a family with piebaldism affecting four successive generations. The disease was present in 16 members of the family.
L K, Gupta, S, Maru, A, Mittal, B L, Masuria, M, Sharma, N K, Bansal   +5 more
openaire   +1 more source

Piebaldism [PDF]

, 2020
openaire   +3 more sources