Atherton D

Guy's and St Thomas' NHS Foundation Trust

2
EM Publications
17
h-index
(795 citations, 44 total works)

Research Topics

Cleft Lip and Palate Research (16) Reconstructive Surgery and Microvascular Techniques (11) Craniofacial Disorders and Treatments (7) Pain Mechanisms and Treatments (5) Nasal Surgery and Airway Studies (5)

Erythromelalgia Publications

Treatment with carbamazepine and gabapentin of a patient with primary erythermalgia (erythromelalgia) identified to have a mutation in the SCN9A gene, encoding a voltage-gated sodium channel.

Natkunarajah J, Atherton D, Elmslie F, Mansour S, Mortimer P
Clinical and experimental dermatology

Primary erythermalgia (erythromelalgia) is a rare autosomal dominant condition characterized by intermittent attacks of erythema, increased skin temperature and severe burning pain in the extremities, in a bilateral symmetrical distribution. Mutations in the SCN9A gene, which encodes a voltage-gated sodium channel have been shown to cause this disease. We report a family identified to have a mutation in the SCN9A gene, in which one severely affected family member has responded to the therapeutic combination of gabapentin and carbamazepine treatment.

Erythromelalgia: an endothelial disorder responsive to sodium nitroprusside.

Chan MK, Tucker AT, Madden S, Golding CE, Atherton DJ , et al.
Archives of disease in childhood

Erythromelalgia is an unusual syndrome of painful vasodilatation. Aetiopathology is probably different in children and adults. Presentation can be severe and associated with hypertension. Dramatic benefit from infused nitroprusside suggests the disorder could represent a dysfunctional endothelium.