Manifestations of pseudoxanthoma elasticum in childhood

M Naouri1, C Boisseau, P Bonicel

  • 1PXE Consultation Centre, Orléans Hospital, Orléans, France.

Insights

Pseudoxanthoma elasticum (PXE) often presents with skin issues in children, but serious complications are rare during childhood. Early diagnosis of PXE is crucial for managing the condition and improving long-term outcomes.

Area of Science:

  • Genetics and rare diseases
  • Dermatology
  • Ophthalmology
  • Cardiovascular medicine

Background:

  • Pseudoxanthoma elasticum (PXE) is a genetic disorder affecting skin, retina, and cardiovascular system, typically diagnosed late.
  • Most PXE cases stem from mutations in the ABCC6 gene.

Purpose of the Study:

  • To characterize the clinical manifestations of PXE in patients under 15 years old.
  • To identify early signs and potential complications of PXE in pediatric populations.

Main Methods:

  • Evaluation of children under 15 with confirmed PXE at a specialized center.
  • Retrospective review of adult patients with severe PXE manifestations before age 15.

Main Results:

  • 16% of 96 patients had pediatric onset; 15 had symptoms before age 15.
  • Cutaneous lesions were the primary symptom in pediatric cases; no ocular or cardiovascular issues were noted in childhood.
  • Six adults reported severe manifestations before age 15, including two with GGCX-related PXE-like conditions.

Conclusions:

  • PXE's cutaneous signs in children mirror those in young adults.
  • While complications are uncommon in childhood, severe outcomes can be unpredictable.
  • Early PXE diagnosis in children is vital for prognosis, enabling lifestyle advice and management.
Abstract

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