Case study fetal abnormality

A genetic disorder is a health problem caused by one or more abnormalities in the genome. It can be caused by a mutation in a single gene monogenic or multiple genes polygenic or by a chromosomal abnormality. Although polygenic disorders are the most common, the term is mostly used when discussing disorders with a single genetic cause, either in a gene or chromosome. When the genetic disorder is inherited from one or both parents, it is also classified as a hereditary disease.
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Moral Status Case Study Fetal Abnormality (Research Paper Sample)

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Fetal Abnormality and Ethical Dilemms of Abortion | Free Essay Example

PLOS Medicine 18 1 : e PLOS Medicine 14 3 : e Perinatal mortality and morbidity continue to be major global health challenges strongly associated with prematurity and reduced fetal growth, an issue of further interest given the mounting evidence that fetal growth in general is linked to degrees of risk of common noncommunicable diseases in adulthood. Against this background, WHO made it a high priority to provide the present fetal growth charts for estimated fetal weight EFW and common ultrasound biometric measurements intended for worldwide use. We conducted a multinational prospective observational longitudinal study of fetal growth in low-risk singleton pregnancies of women of high or middle socioeconomic status and without known environmental constraints on fetal growth.
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Fetal Abnormality

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Metrics details. The aim of this qualitative study was to understand why some women are late to access antenatal care. Interviews were transcribed verbatim and entered onto NVivo 8 software. An interdisciplinary, iterative, thematic analysis was undertaken. The late booking women were diverse in terms of: age 15—37 years ; parity 0—4 ; socioeconomic status; educational attainment and ethnicity.
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