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.
|Published (Last):||13 January 2007|
|PDF File Size:||19.11 Mb|
|ePub File Size:||12.22 Mb|
|Price:||Free* [*Free Regsitration Required]|
It appears that you already have a Toluna account. Type I cytokine receptor: Reconnect now Disconnect my Facebook account for now. InfancyNeonatal ICD D ICD – Views Read Edit View history.
Users should refer to the original published version of the material for the full abstract.
Piebaldism is completely unrelated to acquired or infectious conditions such as vitiligo or poliosis. For all other comments, please send your remarks via contact us. In albinism the cells lack the ability to produce pigment altogether.
Seminars in Cutaneous Medicine and Surgery.
It has been linked to inactivating mutations or deletions of the c-Kit gene. FZD4 Familial exudative vitreoretinopathy 1.
There is nevertheless great variation in the degree and pattern of presentation, even within affected families. Piebaldism This condition affects melanocyte development Classification and external resources Specialty endocrinology [ edit on Wikidata ]. Albinism Oculocutaneous albinism Ocular albinism.
EBSCOhost | | Piebaldismo.
Carotenosis Tattoo Tar melanosis. Amino acid metabolism disorders Autosomal dominant disorders Disturbances of human pigmentation Disturbances of pigmentation. Alezzandrini syndrome Vogt—Koyanagi—Harada syndrome.
Other search option s Alphabetical list. You can too by signing up now! Sign Up Sign in. Argyria Chrysiasis Arsenic poisoning Lead poisoning Titanium metallic discoloration. The vision problems associated with albinism are not usually present as eye pigmentation is normal.
Piebaldismo, importancia de su seguimiento | Roberto Glorio –
However, remote access to EBSCO’s databases from non-subscribing institutions is not allowed if the purpose of the use is for commercial gain through cost reduction or avoidance for a non-subscribing institution.
Historically, persons with extensive piebaldism have experienced abuse of the sort still suffered in the present by albinos, especially in Africa.
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 cases with hypopigmented and depigmented eyebrows and eyelashes.
Piebaldism is a rare autosomal dominant disorder of melanocyte development. No warranty is given about the accuracy of the copy. It has been documented to occur in all races; piebqldismo 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.