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Kalsi, Henna

Mayo Clinic

Mayo Clinic in Arizona

Citations 2

Severe case and literature review of primary erythromelalgia: Novel SCN9A gene mutation
Rooke, Thom W. , Davis, Mark D.P. , Kalsi, Henna, Kurth, Ingo , Richardson, Randal , Skeik, Nedaa , Davis, Dawn Marie R.

Vascular Medicine | October 27, 2011 | Volume: 17 | Issue: 1 | Pages: 44-49

10.1177/1358863x11422584 Get It

Erythromelalgia is a rare clinical syndrome characterized by intermittent heat, redness, swelling and pain more commonly affecting the lower extremities. Symptoms are mostly aggravated by warmth and are eased by a cold temperature. In some cases, symptoms can be very severe and disabling. Erythromelalgia can be classified as either familial or sporadic, with the familial form inherited in an autosomal dominant manner. Recently, there has been a lot of progress in studying Na(v)1.7 sodium channels (expressed mostly in the sympathetic and nociceptive small-diameter sensory neurons of the dorsal root ganglion) and different mutations affecting the encoding SCN9A gene that leads to channelopathies responsible for some disorders, including primary erythromelalgia. We present a severe case of progressive primary erythromelalgia caused by a new de novo heterozygous missense mutation (c.2623C>G) of the SCN9A gene which substitutes glutamine 875 by glutamic acid (p.Q875E). To our knowledge, this mutation has not been previously reported in the literature. We also provided a short literature review about erythromelalgia and Na(v) sodium channelopathies.
Fibrin D-Dimer Concentration, Deep Vein Thrombosis Symptom Duration, and Venous Thrombus Volume
Kurklinsky, Andrew K., Kalsi, Henna, Wysokiński, Waldemar E. , Mauck, Karen F. , Bhagra, Anjali , Havyer, Rachel D. , Thompson, Carrie A. , Hayes, Sharonne N. , McBane, Robert D. , Wysokinski, Waldemar , McBane, Robert , Hayes, Sharonne N

Angiology | September 11, 2010 | Volume: 62 | Issue: 3 | Pages: 253-256

10.1177/0003319710382416 Get It

Introduction: To determine the relationship between fibrin D-dimer levels, symptom duration, and thrombus volume, consecutive patients with incident deep venous thrombosis (DVT) were evaluated. Methods: In a cross-sectional study design, patient symptom onset was determined by careful patient questioning. Venous thrombosis was confirmed by compression duplex ultrasonography. Thrombus volume was estimated based on patient’s femur length using a forensic anthropology method. Fibrin D-dimer was measured by latex immunoassay. Results: 72 consecutive patients with confirmed leg DVT agreed to participate. The median symptom duration at the time of diagnosis was 10 days. The median D-dimer concentration was 1050 ng/dL. The median thrombus volume was 12.92 cm 3 . D-Dimer levels correlated with estimated thrombus volume (P < .0006 CI 0.12-0.41; R 2 adjusted = .15) but not symptom duration, patient’s age, or gender. Conclusions: Despite varying symptom duration prior to diagnosis, fibrin D-dimer remains a sensitive measure of venous thrombosis and correlates with thrombus volume.