A case of a Japanese neonate with congenital ichthyosiform erythroderma diagnosed as Netherton syndrome

Clin Exp Dermatol. 2006 Sep;31(5):677-80. doi: 10.1111/j.1365-2230.2006.02207.x.

Abstract

We report a 6-day-old Japanese girl showing generalized erythroderma accompanied by yellowish, exfoliative scaling that was accentuated on the face and scalp. Histological analysis showed psoriasiform dermatitis with acanthotic epidermis and premature shedding of the stratum corneum. Measurement of trypsin-like hydrolytic activity in SC showed six-fold greater activity compared with age-matched controls. DNA analysis revealed two mutations, 375delAT and 966insC, in exons 5 and 11, respectively, of the SPINK5 gene. Although at 4 weeks the child was still too young to display characteristic hair abnormalities or atopic diathesis, we diagnosed Netherton syndrome based on enzyme assay and DNA analysis.

Publication types

  • Case Reports

MeSH terms

  • Carrier Proteins / genetics*
  • DNA Mutational Analysis
  • Exons
  • Female
  • Gene Deletion*
  • Hair / abnormalities*
  • Humans
  • Ichthyosiform Erythroderma, Congenital / genetics*
  • Infant, Newborn
  • Proteinase Inhibitory Proteins, Secretory
  • Serine Peptidase Inhibitor Kazal-Type 5
  • Serine Proteinase Inhibitors / genetics*
  • Syndrome

Substances

  • Carrier Proteins
  • Proteinase Inhibitory Proteins, Secretory
  • SPINK5 protein, human
  • Serine Peptidase Inhibitor Kazal-Type 5
  • Serine Proteinase Inhibitors