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Partial Albinism
NADINE G. SMITH, M.D.;
JEANETTE SCHULZ, M.D.
AMA Arch Derm. 1955;71(4):468-470.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings. |
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Partial albinism is inherited as a dominant Mendelian characteristic. It consists of patches of depigmentation and usually a white forelock. There is confusion about the disorder and its relation to vitiligo. Dermatologic texts discuss this clinical picture with universal albinism and fail to draw a clear distinction between the two. The latter is usually a recessive trait in which there is a melanin deficit in the retina, iris, and hair, in addition to the skin. There are frequently other associated congenital abnormalities in total albinism but not in partial albinism. Universal albinism is much more common than the partial variety. The term vitiligo should not be applied to partial albinism although microscopically they cannot be differentiated. The former is by definition an acquired depigmentation. Vitiliginous lesions have hyperpigmented borders and frequently change in size, features which are not present in piebaldism. In the literature there is a
. . . [Full Text PDF of this Article]
Author Affiliations
Minneapolis
From the Department of Dermatology, Minneapolis General Hospital (Carl W. Laymon, M.D., Chairman) and from the Department of Pediatrics (Richard B. Raile, M.D., Chairman).
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