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Gerpen, Jay Van

Mayo Clinic

Department of Neurology, Clinical Genomics Jacksonville FL United States

Citations 16

Novel GFAP Variant in Adult-onset Alexander Disease With Progressive Ataxia and Palatal Tremor
Gass, Jennifer , Cheema, Anvir, Jackson, Jessica L. , Blackburn, Patrick R. , Gerpen, Jay Van, Gerpen, Jay A. van, Atwal, Paldeep S

The Neurologist | October 31, 2017 | Volume: 22 | Issue: 6 | Pages: 247-248

10.1097/nrl.0000000000000153 Get It

Introduction: Alexander disease is a rare neurodegenerative disease caused by variants in the glial fibrillary acidic protein gene (GFAP). This disorder can develop as an infantile, juvenile or adult-onset form and is characterized by several clinical features, including macrocephaly, seizures, ataxia, and bulbar/pseudobulbar signs. While the majority of these patients have the more progressive infantile form which causes severe leukodystrophy and early death; the less common adult form is more variable (ie, onset age, symptoms), with bulbar dysfunction as the primary feature. Case Report: In our investigation, we describe a patient with progressive neuromuscular issues including dyspnea, dysphagia, dysarthria and progressive ataxia with palatal tremor. Conclusions: Through genetic testing, we determined that our patient has a novel variant in GFAP typical of Alexander disease.
Expanded phenotype in a patient with spastic paraplegia 7
Gass, Jennifer , Blackburn, Patrick R. , Jackson, Jessica L. , Macklin, Sarah , Gerpen, Jay Van, Atwal, Paldeep S. , Jackson, Jessica, Van Gerpen, Jay, Atwal, Paldeep S , Gerpen, Jay A. van

Clinical Case Reports | August 24, 2017 | Volume: 5 | Issue: 10 | Pages: 1620-1622

10.1002/ccr3.1109 Get It

Key Clinical MessageHereditary spastic paraplegia is a group of clinically and genetically heterogeneous neurodegenerative disorders, often characterized by weakness and spasticity in the lower limbs. In our study, we describe a spastic paraplegia type 7 patient with an expanded phenotype who was diagnosed after the discovery of pathogenic variants in SPG7.
A Case of Two Repeats: Huntington's Disease and Spinocerebellar Ataxia Type 8
Gass, Jennifer , McKay, Jake H., Guthrie, Kimberly J., Boczek, Nicole J. , Gerpen, Jay Van, Gass, Jennifer M, McKay, Jake, Boczek, Nicole, Atwal, Paldeep S. , Van Gerpen, Jay, Atwal, Paldeep S , Gerpen, Jay A. van

Movement Disorders Clinical Practice | July 23, 2016 | Volume: 4 | Issue: 2 | Pages: 270-272

10.1002/mdc3.12401 Get It

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DIRECTED AGGRESSIVE BEHAVIOR IN FRONTAL LOBE EPILEPSY: A VIDEO-EEG AND ICTAL SPECT CASE STUDY
Shih, Jerry J. , Leslie‐Mazwi, Thabele M , Falcao, Germano, Gerpen, Jay Van, Gerpen, Jay A. van

Neurology | October 22, 2009 | Volume: 73 | Issue: 21 | Pages: 1804-1806

10.1212/wnl.0b013e3181c2933f Get It