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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Available on Available on. We’re working on it Piebaldism Waardenburg syndrome Tietz syndrome. Piebaldism is completely unrelated to acquired or infectious conditions such as vitiligo or poliosis. No warranty is given about the accuracy of the copy.

EBSCOhost | | Piebaldismo.

Sign Up Sign in. Dyschromatosis symmetrica hereditaria Dyschromatosis universalis hereditaria. Reconnect now Disconnect my Facebook account for now. To learn more about the cookies we use, check out our Cookies policy. Join and start sharing your opinions with piebalrismo world By signing up you accept our terms of use and privacy policy.

Our website uses cookies. In some cases, piebaldism occurs together with severe developmental problems, as in Waardenburg syndrome and Hirschsprung’s disease. 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.

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Piebaldism differs from albinism in that the affected cells maintain the ability to produce pigment but have that specific function turned off. This section needs expansion. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Incontinentia pigmenti Scratch piebaldimo Shiitake mushroom dermatitis.

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Acanthosis nigricans Freckle Familial progressive hyperpigmentation Pallister—Killian syndrome Periorbital hyperpigmentation Photoleukomelanodermatitis of Kobori Postinflammatory hyperpigmentation Transient neonatal pustular melanosis.

Piebaldism This condition affects melanocyte development Classification and external resources Specialty endocrinology [ edit on Wikidata ].

Oculocutaneous albinism Ocular albinism. It has been documented to occur in 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 piebaldisom were affected by piebaldism.


This is an autosomal dominant [3] hereditary condition, which tends to produce high rates of inheritance and long piebaaldismo of generational transmission.

piebaldismo – English Translation – Word Magic Spanish-English Dictionary

Views Read Edit View history. The vision problems associated with albinism are not usually present as eye pigmentation is normal. Health care resources for this disease Expert centres 56 Diagnostic tests 17 Patient organisations 20 Orphan drug s 0.

Skin color Skin whitening Tanning Sunless.


Other search option s Alphabetical list. These mutations result in a decrease piebalfismo the receptor tyrosine kinase signalling. By using this site, you agree to the Terms of Use and Privacy Policy.

Log in to Toluna. Amino ppiebaldismo metabolism disorders Autosomal dominant disorders Disturbances of human pigmentation Disturbances of pigmentation. Argyria Chrysiasis Arsenic poisoning Lead poisoning Titanium metallic discoloration. Check this box if you wish to receive a copy of your message. What do you think?

Embed this thumb it on your blog. Nevus depigmentosus Postinflammatory hypopigmentation Pityriasis alba Vagabond’s leukomelanoderma Yemenite deaf-blind hypopigmentation syndrome Wende—Bauckus syndrome.