[Harlequin phenomenon associated with neurological abnormalities: A case report]
P Lucas1, L Legendre1, C Pauwels1
1Service de dermatologie, centre de référence des maladies rares de la peau, hôpital Larrey, CHU, 24, chemin de Pouvourville, 31059 Toulouse, France.
Harlequin phenomenon, a rare autonomic neuropathy, presents with facial flushing and sweating abnormalities. This case highlights its association with Horner syndrome and developmental delays in a child.
Area of Science:
- Neurology
- Autonomic Nervous System Disorders
Background:
- Harlequin phenomenon is characterized by unilateral facial flushing and sweating, with contralateral anhidrosis.
- It results from autonomic neuropathy affecting sympathetic vasodilator neurons.
Observation:
- A 9-year-old boy presented with unilateral facial erythema and Horner's syndrome.
- His medical history included generalized myoclonic epilepsy, psychomotor delay, and mental retardation.
Findings:
- The patient was diagnosed with Harlequin phenomenon.
- This case is the first reported instance of Harlequin phenomenon associated with Horner syndrome, epilepsy, and developmental delays.
Implications:
- Clinicians should recognize Harlequin phenomenon due to its distinct presentation.
- Awareness is crucial for timely diagnosis and investigation of associated conditions.
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