Piebaldism is a rare autosomal dominant disorder of melanocyte development.: Common characteristics include a congenital white forelock, scattered. Abstract. AVINA FIERRO, Jorge Arturo and HERNANDEZ AVINA, Daniel Alejandro. Piebaldism, partial albinism in the hair and the skin. Rev Cubana Pediatr. Piebaldismo, import ancia de su seguimient o zyxwvutsrqponm Robert o Glor¡ o\ o Carbia^, Alberto Solari^ y Alberto W oscof f RES UMEN: El piebaldism o es.
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Historically, persons with extensive piebaldism have experienced abuse of the sort still suffered in the present by albinos, especially in Africa.
Alezzandrini syndrome Vogt—Koyanagi—Harada syndrome. Dyschromatosis symmetrica hereditaria Dyschromatosis universalis hereditaria.
It has been documented to occur pieebaldismo all races; early photographers captured many images of African piebalds used as a form of amusement, and George Catlin is believed to have painted several portraits of Native Americans of the Mandan tribe who were affected by piebaldism.
PTH1R Jansen’s metaphyseal chondrodysplasia. For all other comments, please send your remarks via contact us.
This section needs expansion. It appears piebalsismo you already have a Toluna account. FZD4 Familial exudative vitreoretinopathy 1.
Piebaldism is a kind of neurocristopathyinvolving defects of various neural crest cell lineages that include melanocytes, but also involving many other tissues derived from the neural crest.
Piebaldism Waardenburg syndrome Tietz syndrome.
Dermatopathia pigmentosa reticularis Pigmentatio reticularis faciei et colli Reticulate acropigmentation of Kitamura Reticular pigmented anomaly of the flexures Naegeli—Franceschetti—Jadassohn syndrome Dyskeratosis congenita X-linked reticulate pigmentary disorder Galli—Galli disease Revesz syndrome. Greicy12 is using Toluna to voice opinions and earn great rewards.
Rebecca Heckard, la modella affetta da piebaldismo
Our Privacy Notice governs your membership of our Influencer Panel, which you can access here. Users should refer to the original published piebalcismo of the material for the full abstract. What do you think? Argyria Chrysiasis Arsenic poisoning Lead poisoning Titanium metallic discoloration. Log in to Toluna or. We’re working on it Piebaldism This condition affects melanocyte development Classification and external resources Specialty endocrinology [ edit on Wikidata ].
EBSCOhost | | Piebaldismo.
Skin color Skin whitening Tanning Sunless. Type I cytokine receptor: The National Organization of Albinism and Hypopigmentation, as well as organizations such as Under the Same Sunwork to promote awareness of all forms of cutaneous variation and their medical implications, and to highlight human rights issues, especially the plight of albinos subject to extreme persecution in parts of Africa.
Additional information Further information on this disease Classification s 2 Gene s 2 Clinical signs and symptoms Publications in PubMed Other website s 3. InfancyNeonatal Piebaldisom The vision problems associated with albinism are not usually present as eye pigmentation is normal.
Disease definition Piebaldism is a rare congenital pigmentation skin disorder characterized by the presence of hypopigmented and depigmented skin areas leukoderma on various parts of the body, preferentially on the forehead, chest, abdomen, upper arms, and lower extremities, that are associated with a white forelock poliosisand in some piebaldis,o with hypopigmented and depigmented eyebrows piebaldismmo eyelashes.
To learn more about the cookies we use, check out our Cookies policy. Carotenosis Tattoo Tar melanosis. From Wikipedia, the free encyclopedia. Specialised Social Services Eurordis directory.
Here’s a quick tour of a few features to help you get the maximum out of our site. In some cases, piebaldism occurs together with severe developmental problems, as in Waardenburg syndrome and Hirschsprung’s disease.
This page was last edited on 14 Mayat Your Facebook token has expired, you need to reconnect your Toluna account with Facebook or disconnect the two accounts for now. Piebaldism differs from albinism in that the affected cells maintain the ability to produce pigment but have that specific function turned off. CASR Familial hypocalciuric peibaldismo.
Nevus depigmentosus Postinflammatory hypopigmentation Pityriasis alba Vagabond’s leukomelanoderma Yemenite deaf-blind hypopigmentation syndrome Wende—Bauckus syndrome.