Results 141 to 150 of about 1,435 (174)

Waardenburg Syndrome in a Family.

Int J Trichology
Niveditha M, Prathap P, Asokan N.
europepmc   +1 more source

Progressive intertriginous plaques in a patient with fatigue and diarrhea. [PDF]

JAAD Case Rep
Momin B, Martini A, Fike J.
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Alezzandrini syndrome mimicking shingles - A rare case report with review of literature.

Oman J Ophthalmol
Singh M, Kumari R, Onkar A, Das S, Pal T, Saha BC.   +5 more
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Human genomic tools to assess missense variant pathogenicity in domestic mammals using a mock-variant strategy. [PDF]

Open Vet J
Hu H, Xie W.
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Familial Case of Piebaldism

Annals of Clinical and Analytical Medicine, 2013
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Rubinstein-Taybi syndrome with piebaldism

Clinical and Experimental Dermatology, 1994
A young girl is reported suffering from multiple congenital anomalies typical of Rubinstein-Taybi syndrome, in association with cutaneous lesions of piebaldism and occipital poliosis. Clinical characteristics of both entities are described and cutaneous manifestations of Rubinstein-Taybi syndrome are reviewed.
P, Herranz, J, Borbujo, W, Martínez, C, Vidaurrázaga, R, Diaz, M, Casado   +5 more
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Congenital Deafness Associated With Piebaldness

Archives of Otolaryngology - Head and Neck Surgery, 1965
DURING a study of the frequency of generalized albinism in the various Indian populations occurring in the southwestern part of the United States, two Hopi male siblings with piebaldness (partial albinism) and congenital deafness were encountered. 15 Since this syndrome has never been presented before, and these siblings, born in 1952 and 1956, show a ...
C M, WOOLF, D A, DOLOWITZ, H E, ALDOUS
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Piebaldism

Cosmoderma, 2022
Aravind Sivakumar, Deepti Singh
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The Color Piebald

World Literature Written in English, 1996
Tuzyline Jita Allan, Womanist and Feminist Aesthetics: A Comparative Review. Athens: Ohio University Press, 1995, 152pp.
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[Piebaldism].

Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1987
Piebaldism is a rare, congenital, autosomal dominant inherited pigmentary disorder, characterized by a white forelock and freckled depigmentation of the forehead, chin, ventral trunk and extremities. Normal pigmentation is found on the back, hands and feet. Within the non-pigmented areas, patches of hyperpigmentation are possible.
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