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Rao, Chethan K.

https://orcid.org/0000-0003-3529-2018

Mayo Clinic

Nemours Children's Health System

Citations 4

Super-Refractory Status Epilepticus During Blinatumomab Initiation for B-Cell Acute Lymphoblastic Leukemia
Rao, Chethan K. , Kamoroff, Samuel, Zorrilla, Julian, Joyce, Michael , Galán, Fernando , Kamoroff, Samuel , Galan, Fernando N , Kamoroff, Sam , Joyce, Michael

Immunotherapy | January 9, 2023 | Volume: 14 | Issue: 18 | Pages: 1437-1442

10.2217/imt-2021-0344 Get It

A Novel Mutation in Lafora Disease and Update on Pathophysiology and Future Treatments
Nordli, Douglas R. , Rao, Chethan K. , Galán, Fernando , Galan, Fernando N , Nordli Iii, Douglas R , Delgado‐Escueta, Antonio V.

Child Neurology Open | October 5, 2022 | Volume: 9 | Issue: No issue available | Pages: No page available

10.1177/2329048x221126361 Get It

Lafora disease is a rare refractory epilepsy that results in death. This report highlights two cases of lafora disease and introduces a novel mutation in the patients. A review of the pathophysiology and future therapies is reviewed.
Teaching NeuroImage: Pseudo–Figure-of-4 Sign
Rao, Chethan K. , Tatum, William O.

Neurology | October 21, 2021 | Volume: 98 | Issue: 3 | Pages: No page available

10.1212/wnl.0000000000013003 Get It

Post–COVID-19 Acute Disseminated Encephalomyelitis in a 17-Month-Old
McLendon, Loren , Rao, Chethan K. , Hora, Cintia Carla Da, Islamovic, Florinda , Galán, Fernando , McLendon, Loren A, Galan, Fernando N , McLendon, Loren A , Hora, Cintia Carla da

Pediatrics | March 24, 2021 | Volume: 147 | Issue: 6 | Pages: No page available

10.1542/peds.2020-049678 Get It

Neurologic manifestations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in pediatric patients have been reported in the acute and postinfectious stages of coronavirus disease 2019. Acute disseminated encephalomyelitis (ADEM) typically presents in children after a viral illness at a mean age of 3 to 7 years. A total of 60% to 90% of literature-reported pediatric patients with ADEM have minimal to no neurologic deficits at long-term follow-up. We present a 17-month-old developmentally typical girl with parental complaints of irritability, upper extremity weakness, and gait disturbance. She presented to the hospital afebrile and irritable with right-sided nasolabial fold flattening, neck stiffness, left upper extremity rigidity, right upper extremity paresis, bilateral lower extremity hyperreflexia, and truncal ataxia. During her hospital course, she became somnolent with autonomic instability and was transferred to intensive care. Contrasted brain MRI revealed diffuse patchy T2 hyperintensities without contrast enhancement. Nasopharyngeal SARS-CoV-2 polymerase chain reaction and serum antibody testing results were positive. Cerebral spinal fluid analysis was unremarkable. Respiratory viral panel and autoimmune encephalitis and demyelinating disorders panel results were negative. She was started on high-dose methylprednisolone and intravenous immunoglobulin, with improvement in mental status, focal deficits, and ambulation. After hospital discharge, she received inpatient rehabilitation for 2 weeks and at 2 month follow-up had a full neurologic recovery. We report the youngest case of postinfectious ADEM due to SARS-CoV-2 in a toddler. Early recognition of autoimmune and inflammatory complications of SARS-CoV-2 is vital for early aggressive immunomodulatory treatment and, consequently, improved morbidity in these patients.