Significant hearing loss in Fabry disease: Study of the Danish nationwide cohort prior to treatment

Author:

Yazdanfard Puriya Daniel,Madsen Christoffer Valdorff,Nielsen Lars Holme,Rasmussen Åse Krogh,Petersen Jørgen Holm,Seth Alka,Sørensen Søren Schwartz,Køber Lars,Feldt-Rasmussen UllaORCID

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference30 articles.

1. α-Galactosidase A Deficiency: Fabry Disease. OMMBID: The Online Metabolic and Molecular Bases of Inherited Diseases;RJ Desnick;α-Galactosidase A Deficiency: Fabry Disease,2013

2. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males;KD Macdermot;J Med Genet,2001

3. X-chromosome inactivation in female patients with Fabry disease;L Echevarria;Clin Genet,2016

4. The hearing status in 12 female and 15 male Japanese Fabry patients;Y Sakurai;Auris Nasus Larynx,2009

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