Genetic counseling and screening of sperm donors in the United States

2011 ◽  
Vol 96 (3) ◽  
pp. S91-S92
Author(s):  
L. Isley ◽  
P. Callum
Author(s):  
Guido Pennings ◽  
Edgar Mocanu ◽  
Janne Rothmar Herrmann ◽  
Anne-Bine Skytte ◽  
Corey Burke ◽  
...  

Author(s):  
Kaitlyn Burns ◽  
Amy Swanson ◽  
Jennifer Hoskovec ◽  
Jennifer Leonhard ◽  
Susan Hahn ◽  
...  

2020 ◽  
Vol 29 (2) ◽  
pp. 147-165
Author(s):  
Sabrina V. Southwick ◽  
Riley Esch ◽  
Rachel Gasser ◽  
Deborah Cragun ◽  
Krista Redlinger‐Grosse ◽  
...  

Author(s):  
Pauline Aamodt ◽  
Leah Wetherill ◽  
Paula Delk ◽  
Wilfredo Torres‐Martinez ◽  
Gail H. Vance ◽  
...  

2019 ◽  
Vol 28 (5) ◽  
pp. 962-973 ◽  
Author(s):  
Morgan J. Hnatiuk ◽  
Ryan Noss ◽  
Anna L. Mitchell ◽  
Anne L. Matthews

Author(s):  
Matthew L. Tschirgi ◽  
Kailey M. Owens ◽  
Mia S. Mackall ◽  
Jamie Allen ◽  
Rachel Allen

2008 ◽  
Vol 36 (3) ◽  
pp. 597-601
Author(s):  
Pamela Foohey

Despite exponential growth in the past decades, most aspects of the assisted reproductive technology (ART) industry remain largely unregulated; recently, pressure has been mounting for coordinated study and regulation of this developing industry. On March 28, 2008, lawyers, health care professionals, representatives from sperm banks, consumers of ART services, and other stakeholders in ART industry gathered at DePaul University College of Law for its Health Law Institute’s symposium titled “Tracking Change: The Feasibility of a Voluntary Gamete Donor Registry in the United States.” The implementation of a registry would mark the first effort in the United States to centralize, maintain, and disseminate information about gamete donors by collecting and storing genetic and identifying information about egg and sperm donors. Establishing a registry requires balancing the interests of donor-conceived individuals, their parents, gamete donors, health care professionals, and society as a whole, as well as ensuring the privacy and safety of all involved.


2021 ◽  
Vol 33 (1) ◽  
pp. 29-34
Author(s):  
Christian P. Schaaf

Abstract Genetic counselors represent an indispensable, well-established, and well-integrated group of healthcare providers in the field of genetic and genomic medicine in the United States. They work with other members of the healthcare team to provide information and support to individuals and families concerned with genetic disorders. With more than 5,000 certified genetic counselors in the U.S. and an expected growth of 100 % over the next decade, genetic counseling represents one of the fastest-growing professions in the U.S. Genetic counselors work in clinical environments (e. g., hospitals), in companies (e. g., genetic testing firms), and as consultants to medical practices and others. Twenty-six states license genetic counselors as practitioners who can bill independently, with licensure applications underway in the remaining 24 states. Physicians, genetic counselors, and diagnosticians represent the three pillars of comprehensive, integrated genomic medical care. Within this triad, genetic counselors see their primary role in procuring and interpreting family and medical histories, assessing inheritance, quantifying chances of recurrence, facilitating decision-making regarding genetic testing options, and explaining the results of such testing to the respective individuals within the greater context of their families.


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