Steatocystoma multiplex: A rare skin lesion

Authors

  • Anbukkarasi.K
  • Sivaranjani.A
  • Joana Christopher

DOI:

https://doi.org/10.63682/jns.v14i22S.5488

Abstract

Steatocystoma multiplex, a rare genetic condition causes the development of several hamartomatous abnormalities at the pilosebaceous duct junction (the unit that holds the hair follicles). This condition usually arises during the adolescent period. Offspring will surely develop the propensity to form cysts as this is an autosomal dominant disorder and can affect both sexes.

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References

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Published

2025-05-09

How to Cite

1.
Anbukkarasi.K A, Sivaranjani.A S, Christopher J. Steatocystoma multiplex: A rare skin lesion. J Neonatal Surg [Internet]. 2025May9 [cited 2025May15];14(22S):385-9. Available from: https://jneonatalsurg.com/index.php/jns/article/view/5488