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Abstract Details

Evaluation of Clinical Presentation, Skin Biopsy Findings, and Immunologic Testing in Patients with Symptoms of Sensory Neuropathy
Neuromuscular and Clinical Neurophysiology (EMG)
P12 - Poster Session 12 (12:00 PM-1:00 PM)
1-004
To evaluate for correlations between clinical history, exam, and skin biopsy, and immunologic diagnostic results.

Given the advent of wider availability of skin biopsies and specific antibody testing, more objective data is available for evaluating patients with neuropathy. However, this information is often non-diagnostic and requires interpretation within appropriate clinical contexts.

Retrospective chart review of 156 patients with sensory neuropathy symptoms who underwent skin biopsy at Keck Medical Center of USC. Clinic notes, skin biopsy results, and antibody testing were reviewed.

Of the 156 patients reviewed, 109(70%) had abnormal epidermal nerve fiber densities compared to 47(30%) with normal biopsy results. Subjective sensory complaints were similar between both groups, 93.6% and 90.8% of patients, respectively. Objective sensory deficits were reported in 51.1% and 60.6% of patients, respectively. For individuals with prior nerve conduction studies, only 30% of the patients with abnormal biopsies and 25% of the patients with normal biopsies had evidence of large fiber neuropathy on electrodiagnostic testing. Of the 156 patients, 94 had sweat gland nerve fiber densities analyzed, and 84(89%) had abnormal findings. Of these, only 41(48%) had subjective autonomic complaints, compared to the 2 of 10(20%) patients who had autonomic complaints but normal sweat gland nerve fiber densities. In addition, 39 patients had an antibody sensory neuropathy panel performed; 21 of them had at least 1 positive antibody identified, most often FGFR3 and/or TS-HDS. Of these, 11(52%) had abnormal nerve conduction studies and 19(90.5%) had an abnormal biopsy.

This is a preliminary review of patients who underwent skin biopsy for evaluation of sensory neuropathy. Additional multivariate analyses need to be done to further determine the pathogenic role of antibodies such as FGFR3 and TS-HDS in the clinical presentation of neuropathy, as well as their correlation with physical exam findings, electrodiagnostic testing, and skin biopsy results. 
Authors/Disclosures
Norianne Pimentel, MD (University of Southern California, LA County, Child Neurology)
PRESENTER
No disclosure on file
Leila Darki, MD, FÂé¶¹´«Ã½Ó³»­ (USC NeuroSciences) Dr. Darki has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Trinity Partner. Dr. Darki has received personal compensation in the range of $0-$499 for serving as a Consultant for Guide point Global. Dr. Darki has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Global Access Meetings. Dr. Darki has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Amylyx . Dr. Darki has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Amylyx.
Said R. Beydoun, MD, FÂé¶¹´«Ã½Ó³»­ (University of Southern California Healthcare Consultation Center 2) Dr. Beydoun has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Amgen. Dr. Beydoun has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Alexion. Dr. Beydoun has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Janssen. Dr. Beydoun has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for CSL. Dr. Beydoun has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for AstraZeneca. Dr. Beydoun has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Argenx. Dr. Beydoun has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for UCB. Dr. Beydoun has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Pfizer. Dr. Beydoun has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Takeda. Dr. Beydoun has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for Alnylam. Dr. Beydoun has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Alexion. Dr. Beydoun has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for CSL. Dr. Beydoun has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for UCB. Dr. Beydoun has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Takeda. Dr. Beydoun has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for AstraZeneca. Dr. Beydoun has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Argenx. Dr. Beydoun has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for Janssen. The institution of Dr. Beydoun has received research support from Abcuro. The institution of Dr. Beydoun has received research support from Sean Healy & AMG Center for ALS. The institution of Dr. Beydoun has received research support from Regeneron. The institution of Dr. Beydoun has received research support from RemeGen. The institution of Dr. Beydoun has received research support from Sanofi. The institution of Dr. Beydoun has received research support from Novartis.