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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.
Background:
Pseudoxanthoma elasticum (PXE) affects the skin, retina and cardiovascular system. Most cases are related to mutations in the ABCC6 gene. The diagnosis is most often made late in the second or third decade of life.
Objectives:
To describe the manifestations of PXE before the age of 15 years.
Methods:
Children under age 15 years with definite PXE were evaluated at a PXE referral centre, as were adult patients in whom serious manifestations of PXE had occurred before the age of 15 years.
Results:
Our series included 96 patients; 15 (16%) had paediatric onset of the disease. Nine children were diagnosed at a mean age of 10 years, a mean of 2.5 years after the presenting symptoms. Cutaneous lesions were the presenting symptoms in eight. None had cardiovascular or ophthalmological symptoms. Six adult patients had had severe cutaneous and/or cardiovascular manifestations before the age of 15 years. Both adult patients with early extensive skin lesions had the PXE-like condition related to the GGCX gene. No ocular symptoms were recorded during childhood.
Conclusions:
Cutaneous manifestations of PXE are the same in children as in young adults. Absence of complications is common in childhood, but severe complications are unpredictable. The frequency of complications was retrospectively estimated to be 7% in the adults of our series, although this figure was probably an overestimate because of the recruitment bias in a referral centre. It is, however, important to consider PXE in the paediatric setting, as early diagnosis may be important to provide accurate information and discuss lifestyle adjustments in order to improve the prognosis of the disease.
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