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COVID-19 in people with neurofibromatosis 1, neurofibromatosis 2, or schwannomatosis.
Banerjee, Jineta; Friedman, Jan M; Klesse, Laura J; Yohay, Kaleb H; Jordan, Justin T; Plotkin, Scott R; Allaway, Robert J; Blakeley, Jaishri O.
  • Banerjee J; Sage Bionetworks, Seattle, WA.
  • Friedman JM; Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Klesse LJ; Division of Hematology/Oncology, Department of Pediatrics, UT Southwestern Medical Center, Dallas, TX.
  • Yohay KH; Departments of Neurology and Pediatrics, NYU Langone Health, New York, NY.
  • Jordan JT; Stephen E. and Catherine Pappas Center for Neuro-Oncology, Massachusetts General Hospital, Boston, MA.
  • Plotkin SR; Stephen E. and Catherine Pappas Center for Neuro-Oncology, Department of Neurology and Cancer Center, Massachusetts General Hospital, Boston, MA.
  • Allaway RJ; Sage Bionetworks, Seattle, WA. Electronic address: robert.allaway@sagebionetworks.org.
  • Blakeley JO; Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD. Electronic address: jblakel3@jhmi.edu.
Genet Med ; 25(2): 100324, 2023 02.
Article in English | MEDLINE | ID: covidwho-2178938
ABSTRACT

PURPOSE:

People with pre-existing conditions may be more susceptible to severe COVID-19 when infected by SARS-CoV-2. The relative risk and severity of SARS-CoV-2 infection in people with rare diseases such as neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), or schwannomatosis (SWN) is unknown.

METHODS:

We investigated the proportions of people with NF1, NF2, or SWN in the National COVID Cohort Collaborative (N3C) electronic health record data set who had a positive test result for SARS-CoV-2 or COVID-19.

RESULTS:

The cohort sizes in N3C were 2501 (NF1), 665 (NF2), and 762 (SWN). We compared these with N3C cohorts of patients with other rare diseases (98-9844 individuals) and the general non-NF population of 5.6 million. The site- and age-adjusted proportion of people with NF1, NF2, or SWN who had a positive test result for SARS-CoV-2 or COVID-19 (collectively termed positive cases) was not significantly higher than in individuals without NF or other selected rare diseases. There were no severe outcomes reported in the NF2 or SWN cohorts. The proportion of patients experiencing severe outcomes was no greater for people with NF1 than in cohorts with other rare diseases or the general population.

CONCLUSION:

Having NF1, NF2, or SWN does not appear to increase the risk of being SARS-CoV-2 positive or of being a patient with COVID-19 or of developing severe complications from SARS-CoV-2.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Neurofibromatosis 2 / Neurofibromatosis 1 / Neurofibromatoses / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: Genet Med Journal subject: Genetics, Medical Year: 2023 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Neurofibromatosis 2 / Neurofibromatosis 1 / Neurofibromatoses / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: Genet Med Journal subject: Genetics, Medical Year: 2023 Document Type: Article