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Steatocystomas

Known as: steatocystoma 
 
National Institutes of Health

Papers overview

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2003
2003
BACKGROUND Steatocystoma multiplex is an uncommon disorder which usually begins in adolescence or early adult life. The condition… Expand
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2002
2002
Steatocystoma multiplex (SM) shares many clinical features and may show overlapping histopathological features with eruptive… Expand
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Highly Cited
2002
Highly Cited
2002
Onset of type I keratin 17 (K17) synthesis marks the adoption of an appendageal fate within embryonic ectoderm, and its… Expand
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Highly Cited
1998
Highly Cited
1998
Pachyonychia congenita type 2 (PC-2; Jackson-Lawler syndrome) is an autosomal dominant disorder characterized by hypertrophic… Expand
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Highly Cited
1997
Highly Cited
1997
Pachyonychia congenita (PC) is a group of autosomal dominant ectodermal dysplasias in which the main phenotypic characteristic is… Expand
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1997
1997
We compared the patterns of keratin 10 (K10) and keratin 17 (K17) expression in epidermoid cysts, trichilemmal cysts, eruptive… Expand
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1996
1996
Eruptive vellus hair cysts and steatocystoma multiplex are two clinically similar conditions which show multiple papules and… Expand
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1992
1992
Steatocystoma multiplex (SM) and eruptive vellus hair cysts (EVHC) share a clinical resemblance, but have distinctive histologic… Expand
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Highly Cited
1991
Highly Cited
1991
Five examples of a distinctive sebaceous malformation, designated “folliculosebaceous cystic hamartoma.” form the basis of this… Expand
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1982
1982
Steatocystoma simplex, an entity not previously described, to my knowledge, occurred in 16 women and 14 men. Eleven cysts were… Expand
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