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Precision Health and Deafness: Optimizing Genetic Diagnosis

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개인저자Sloan-Heggen, Christina Marie.
단체저자명The University of Iowa. Molecular Physiology & Biophysics.
서명/저자사항Precision Health and Deafness: Optimizing Genetic Diagnosis.
발행사항[S.l.] : The University of Iowa., 2018
발행사항Ann Arbor : ProQuest Dissertations & Theses, 2018
형태사항191 p.
소장본 주기School code: 0096.
ISBN9780438151253
일반주기 Source: Dissertation Abstracts International, Volume: 79-11(E), Section: B.
Adviser: Richard JH Smith.
요약Deafness is the most common sensory deficit in humans. In the United States 1--2 in a thousand babies is born with significant deafness, well over half of which is hereditary. Providing a patient and their family with a genetic diagnosis is the
요약Targeted genomic enrichment and massively parallel sequencing (TGE+MPS) have revolutionized the field of precision health and medicine, allowing for comprehensive genetic diagnosis of many complicated conditions, including NSHL. To take advantag
요약With the implementation of OtoSCOPERTM we aspire to accomplish two aims: providing comprehensive genetic diagnosis for patients all over the world and characterizing the full spectrum of hereditary hearing loss. The goal of my thesis work has be
요약Finally, we interrogated the contribution of syndromic forms of deafness which may actually manifest as NSHL (NSHL mimics) within two deafness cohorts. We performed a retrospective chart review of 14 families with syndromic deafness seen by the
요약All of these studies have lead to the better understanding of the genes and variants that cause NSHL and its mimics, providing a more accurate genetic diagnosis, which is prerequisite to a future of targeted genetic therapies.
일반주제명Health sciences.
Genetics.
언어영어
기본자료 저록Dissertation Abstracts International79-11B(E).
Dissertation Abstract International
대출바로가기http://www.riss.kr/pdu/ddodLink.do?id=T14996551

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