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Updated: May 3, 2026

Non-invasive Optical Measurement of Cerebral Metabolism and Hemodynamics in Infants
Published on: March 14, 2013
[Inconsolable crying revealing primary erythermalgia in a 6-month-old infant]
Insights
Erythermalgia, a rare vascular condition, was diagnosed in a 6-month-old infant presenting with heat-induced leg redness and pain. This case highlights the condition
Area of Science:
- Pediatric vascular disorders
- Neurology
- Genetics
Background:
- Erythermalgia is a rare peripheral vascular disease triggered by heat.
- The primary infantile form is exceptionally rare, with no prior reported cases in infants.
- Pathophysiology involves sodium channel alterations leading to small-fiber neuropathy.
Observation:
- A 6-month-old infant presented with recurrent crying episodes and lower limb erythema.
- Symptoms were exacerbated by heat and absent in cooler temperatures.
- Standard infant investigations for crying (reflux, intussusception) were negative.
Findings:
- Diagnosis of primary infantile erythralgia was established.
- Genetic mutations in the SCN9A gene are associated with autosomal dominant inheritance.
- Treatment involved analgesics and cold packs, with challenges due to analgesic resistance.
Implications:
- This case expands the known age range for primary erythralgia to infancy.
- Early diagnosis and management are crucial, despite treatment difficulties.
- The condition carries a potentially poor prognosis in the pediatric population.
Abstract:
Erythermalgia is a peripheral vascular disease triggered by exposure to heat. The primary infantile form is rare. No cases have been described in infants. We report a case in a 6-month-old child revealed by crying bouts associated with erythema of the lower limbs. A 6-month-old child was brought in for consultation for daily crying bouts, occurring six times a day, associated with erythema of the lower limbs. Blood count, abdominal ultrasound and endoscopy were normal, excluding gastroesophageal reflux and intussusception. Attacks disappeared during winter but recurred at high temperatures. The diagnosis was primary infant erythemalgia. Treatment with analgesics and ice packs was established. Erythermalgia is a rare peripheral vascular disease characterized by paroxysmal pain triggered by heat and relieved by cold. The primary form occurs in childhood but has never been reported in infants. The pathophysiology is based on an alteration of sodium channels inducing neuropathy in small-caliber fibers. Genetic mutations have been found in the SNC9 gene on chromosome 2q, with autosomal dominant transmission. Support of this condition is difficult due to resistance to conventional analgesics. The prognosis is sometimes poor with a significant death rate in the pediatric population.
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