Journal of Pediatric Research (Jun 2021)

Mucopolysaccharidosis Type-II with Pathognomonic Skin Appearance: A Case with Pebbling Sign

  • Ayşe Hitay İnan,
  • Berna Şeker Yılmaz,
  • Fatma Derya Bulut,
  • Sebile Kılavuz,
  • Deniz Kor,
  • Mehmet Karakaş,
  • Halise Neslihan Önenli Mungan

DOI
https://doi.org/10.4274/jpr.galenos.2020.82621
Journal volume & issue
Vol. 8, no. 2
pp. 206 – 208

Abstract

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Mucopolysaccharidosis type-II (MPS-II) is an X-linked lysosomal storage disorder. Here, we report an 8-year-old boy with pebbling sign in the scapular region, coarse facies, claw hand, diastolic murmur, and hepatomegaly. With decreased iduronate-2-sulfatase activity and hemizygous mutation in the IDS gene, the diagnosis was MPS-II. Pebbling sign is a rare but pathognomonic sign of MPS-II.

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