Hearing loss in individuals with osteogenesis imperfecta in North America: Results from a multicenter study-Reference-Cited by-同舟云学术

Hearing loss in individuals with osteogenesis imperfecta in North America: Results from a multicenter study

Published:2019-12-26 Issue:4 Volume:182 Page:697-704
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Machol Keren¹²^ORCID,Hadley Trevor D.¹,Schmidt Jake¹,Cuthbertson David³,Traboulsi Henri⁴²,Silva Rodrigo C.⁴²,Citron Chloe⁵,Khan Sobiah⁵,Citron Kate⁵,Carter Erin⁵,Brookler Kenneth⁵,Shapiro Jay R.⁶⁷,Steiner Robert D.⁸⁹,Byers Peter H.¹⁰¹¹^ORCID,Glorieux Francis H.¹²,Durigova Michaela¹²,Smith Peter¹³,Bober Michael B.¹⁴,Sutton Vernon R.¹²,Lee Brendan H.¹²,Nagamani Sandesh C. S.¹²,Raggio Cathleen⁵,

Affiliation:

1. Department of Molecular and Human GeneticsBaylor College of Medicine Houston Texas

2. Texas Children's Hospital Houston Texas

3. College of Medicine, University of South Florida Tampa Florida

4. Department of Otolaryngology—Head and Neck SurgeryBaylor College of Medicine Houston Texas

5. Department of Pediatric Orthopedic SurgeryHospital for Special Surgery New York New York

6. Department of Bone and Osteogenesis ImperfectaKennedy Krieger Institute Baltimore Maryland

7. Department of Medicine at Uniformed ServicesUniversity of the Health Sciences Bethesda Maryland

8. University of Wisconsin School of Medicine and Public Health Madison Wisconsin

9. Pediatrics and Molecular and Medical GeneticsOregon Health & Science University Portland Oregon

10. Department of Medicine, Division of Medical GeneticsUniversity of Washington Seattle

11. Department of Pathology, Division of Medical GeneticsUniversity of Washington Seattle

12. Shriner's Hospital for Children and McGill University Montreal Quebec Canada

13. Motion Analysis LaboratoryShriners Hospitals for Children Chicago Illinois

14. Division of OrthogeneticsAlfred I. duPont Hospital for Children Wilmington Delaware

Funder

Intellectual and Developmental Disabilities Research Center

National Center for Advancing Translational Sciences

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61464

Reference27 articles.

1. Four generation of blue sclerotics;Adair‐Dighton C.;Ophthalmoscope,1912

2. Cesarean delivery is not associated with decreased at-birth fracture rates in osteogenesis imperfecta

3. Clinical and Molecular Characterization of Osteogenesis Imperfecta Type V

4. Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

5. Hearing health and care: The need for improved hearing loss prevention and hearing conservation practices

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4. Genetic Evaluation for Monogenic Disorders of Low Bone Mass and Increased Bone Fragility: What Clinicians Need to Know;Current Osteoporosis Reports;2024-04-11

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