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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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.
EBSCOhost | | Piebaldismo.
From Wikipedia, the free encyclopedia. What do you think? It appears that you already have a Toluna account. FZD4 Familial exudative vitreoretinopathy 1.
Retrieved from ” https: Additional information Further information on this disease Classification s 2 Gene s 2 Clinical signs and symptoms Publications in PubMed Other website s 3. PTH1R Jansen’s metaphyseal chondrodysplasia. Oculocutaneous albinism Ocular albinism.
Views Read Edit View history. Piebaldism is an autosomal dominant rare disease characterized by the presence since birth of poliosis and congenital depigmentation white patches on the mid-forehead, chest, abdomen and extremities, where no melanocytes are found.
There is nevertheless great variation in the degree and pattern of presentation, even within affected families.
Rebecca Heckard, la modella affetta da piebaldismo
To learn more about the cookies we use, check out our Cookies policy. Vasospastic macule Woronoff’s ring Nevus anemicus. Albinism Oculocutaneous albinism Ocular albinism. Remote access to EBSCO’s databases is permitted to patrons of subscribing institutions accessing from remote locations for personal, non-commercial use. D ICD – However, remote access to EBSCO’s databases from non-subscribing institutions is not allowed if the purpose of the use is for plebaldismo gain through cost reduction or avoidance for a non-subscribing institution.
Piebaldiwmo is using Toluna to voice opinions and earn great rewards. Health care resources for this disease Expert centres 56 Diagnostic tests 17 Patient organisations 20 Orphan drug s 0. Like in the offline world, cookies make things better. Carotenosis Tattoo Tar melanosis.
Andrews’ Diseases of the Skin: Piebaldism differs from albinism in that the affected cells maintain the ability to produce pigment but have that specific function turned off. Nevus pieabldismo Postinflammatory hypopigmentation Pityriasis alba Vagabond’s leukomelanoderma Yemenite deaf-blind hypopigmentation syndrome Wende—Bauckus syndrome. Available on Available on.
Acanthosis nigricans Freckle Familial progressive hyperpigmentation Pallister—Killian syndrome Periorbital hyperpigmentation Photoleukomelanodermatitis of Kobori Postinflammatory hyperpigmentation Transient neonatal pustular melanosis. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.
Piebaldism – Wikipedia
It is very common in mice, rabbits, dogs, sheep, deer, cattle and horses—where selective breeding has increased the incidence of the mutation- but occurs among chimpanzees and other primates only as rarely as among humans. The vision problems associated with albinism are not usually present as eye pigmentation is normal. This section needs expansion. In albinism the cells lack the ability to produce pigment altogether.
Argyria Chrysiasis Arsenic poisoning Lead poisoning Titanium metallic discoloration. These mutations result in a decrease of the receptor tyrosine kinase signalling.
All who inherit the gene have at some time in life evidence of piebald hypopigmentation of the hair or skin, most likely both.
In some cases, piebaldism occurs together with severe developmental problems, as in Waardenburg syndrome and Hirschsprung’s disease.