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Abstract Details

An Atypical Case of an SCN9A Mutation with Global Motor Delay and Erythromelalgia
Child Neurology/Developmental Neurobiology
P03 - (-)
018
BACKGROUND: Erythromelalgia is characterized by recurrent episodes of burning pain and redness of the extremities and is caused by heterozygote gain-of-function mutations in the SCN9A gene, coding for the NAv1.7 channel. It usually presents as a pure sensory-autonomic disorder. We describe a patient with an SCN9A mutation and an usual phenotypic presentation of gross motor delay, childhood-onset erythromelalgia, extreme visceral pain episodes, followed by hypoesthesia and automutilation.
DESIGN/METHODS: The investigation of the patient's motor delay included various biochemical analyses, an EMG, a muscle biopsy, and a quantitative PCR of SMN1. Once erythromelalgia was suspected, the SCN9A gene was sequenced. Sequential therapeutic trials of amitriptyline, gabapentin, carbamazepine and mexiletine were attempted.
RESULTS: The EMG, CGH, EEG and metabolic tests were negative. The sural nerve biopsy showed an axonal neuropathy, whereas the muscle biopsy showed signs of neurogenic atrophy. Sequencing of the SCN9A gene revealed a heterozygote missense mutation in exon 7; p.I234T.
CONCLUSIONS: We present the first case of global motor delay and erythromelalgia associated with an SCN9A mutation. The gross motor delay might be attributed to the extreme pain episodes or to a developmental perturbation of sensory-motor integration.
Authors/Disclosures
Inge Meijer, MD, PhD (CHU Sainte Justine)
PRESENTER
Dr. Meijer has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Allergan. Dr. Meijer has received intellectual property interests from a discovery or technology relating to health care.
No disclosure on file
No disclosure on file
Yves Robitaille, MD, FCAP (CHU Ste-Justine, Dept. of Pathology) No disclosure on file
Elsa Rossignol, MD (Hopital Ste-Justine) No disclosure on file
Bart Van Wijmeersch, MD, PhD (Rehabilitation & MS-Centre Overpelt) Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Sanofi. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Merck. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Celgene/Bristol Myers Group. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Roche. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Janssen Pharmaceutics. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Biogen. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Merck. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Sanofi. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Novartis. Prof. Van Wijmeersch has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Roche. The institution of Prof. Van Wijmeersch has received research support from Merck. The institution of Prof. Van Wijmeersch has received research support from Roche.