Theories Developmental Psychology Problems With Prenatal Development By Kendra Cherry, MSEd Kendra Cherry, MSEd Facebook Twitter Kendra Cherry, MS, is a psychosocial rehabilitation specialist, psychology educator, and author of the "Everything Psychology Book." Learn about our editorial process Updated on July 23, 2020 Fact checked Verywell Mind content is rigorously reviewed by a team of qualified and experienced fact checkers. Fact checkers review articles for factual accuracy, relevance, and timeliness. We rely on the most current and reputable sources, which are cited in the text and listed at the bottom of each article. Content is fact checked after it has been edited and before publication. Learn more. by Adah Chung Fact checked by Adah Chung LinkedIn Adah Chung is a fact checker, writer, researcher, and occupational therapist. Learn about our editorial process Print JGI/Jamie Grill / Getty Images In most cases, prenatal development occurs normally and follows the established patterns of development with little variation. However, a number of things, usually caused by genetics or environmental problems, can go wrong during this time. Genetic Problems Genetics plays a major role in development. In some cases, genetic problems can emerge that may impact both the current and future growth of the developing child in the womb. Down Syndrome: Also known as trisomy 21, Down syndrome is the most common genetic anomaly during prenatal development. Down syndrome is caused by an extra copy of the 21 chromosomes (meaning there are three chromosomes instead of the usual two) and impacts approximately 1 out of every 1,000 infants. Typical features of Down syndrome include flattened facial features, heart defects, and intellectual impairment. The risk of having a child with Down syndrome increases with maternal age.Inherited diseases: A number of illnesses can be inherited if one or both parents carry a gene for the disease. Examples of inherited diseases include sickle-cell anemia, cystic fibrosis, and Tay-Sachs disease. Genetic tests can often determine if a parent is a carrier of genes for a specific disease.Sex-Chromosome Problems: The third type of genetic problem involves sex-chromosomes. These include conditions such as Klinefelter's syndrome (an extra X-chromosome) and Turner syndrome (a single X-chromosome). How Genetics Affect a Child's Development Environmental Problems Environmental variables can also play a major role in prenatal development. Harmful environmental elements that can affect the fetus are known as teratogens. A number of teratogens can harm the fetus, including: Maternal Drug Use: The use of substances by the mother can have devastating consequences to the fetus. Smoking is linked to low birth weight, which can result in a weakened immune system, poor respiration, and neurological impairment. Alcohol use can lead to fetal alcohol syndrome, which is linked to heart defects, body malformations, and intellectual disability. The use of illicit psychoactive drugs such as cocaine and methamphetamine is also linked to low birth weight and neurological impairment. Maternal Disease: A number of maternal diseases can negatively impact the fetus, including herpes, rubella, and AIDS. Herpes virus is one of the most common maternal diseases and can be transmitted to the fetus, leading to deafness, brain swelling, or intellectual disability. Women with herpes virus are often encouraged to deliver via cesarean to avoid transmission of the virus. The prenatal period is a time of tremendous growth and also great vulnerability. A number of dangers can pose a potential risk to the growing fetus. Some of these dangers, such as environmental risks from teratogens and drug use, can be prevented or minimized. In other instances, genetic problems may simply be unavoidable. In either case, early prenatal care can help new mothers and children cope with potential problems with prenatal development. Stages of Prenatal Development 6 Sources Verywell Mind uses only high-quality sources, including peer-reviewed studies, to support the facts within our articles. Read our editorial process to learn more about how we fact-check and keep our content accurate, reliable, and trustworthy. Baburamani AA, Patkee PA, Arichi T, Rutherford MA. New approaches to studying early brain development in Down syndrome. Dev Med Child Neurol. 2019;61:867-879. doi:10.1111/dmcn.14260 Neal SA, Werner MD. The impact of contemporary preimplantation genetic screening and diagnosis on the detection of aneuploidy and inherited genetic diseases. Birth Defects Res. 2018;110(8):644-647. doi:10.1002/bdr2.1220 Haltrich I. Chromosomal Aberrations with Endocrine Relevance (Turner Syndrome, Klinefelter Syndrome, Prader-Willi Syndrome). Exp Suppl. 2019;111:443-473. doi:10.1007/978-3-030-25905-1_20 Cassina M, Cagnoli GA, Zuccarello D, Di Gianantonio E, Clementi M. Human teratogens and genetic phenocopies. Understanding pathogenesis through human genes mutation. Eur J Med Genet. 2017;60(1):22-31. doi:10.1016/j.ejmg.2016.09.011 Williams JF, Smith VC, Committee on Substance Abuse. Fetal Alcohol Spectrum Disorders. Pediatrics. 2015;136(5):31395-e1406. doi:10.1542/peds.2015-3113 Cohen BE, Durstenfeld A, Roehm PC. Viral Causes of Hearing Loss: A Review for Hearing Health Professionals. Trends Hear. 2014;18:2331216514541361. doi:10.1177/2331216514541361 By Kendra Cherry, MSEd Kendra Cherry, MS, is a psychosocial rehabilitation specialist, psychology educator, and author of the "Everything Psychology Book." 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