Long title | To provide health insurance benefits for outpatient and inpatient items and services related to the diagnosis and treatment of a congenital anomaly or birth defect. |
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Announced in | the 117th United States Congress |
Number of co-sponsors | 303 |
Legislative history | |
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The Ensuring Lasting Smiles Act is a proposed United States law that would require private health insurance plans to cover diagnosis and treatment of congenital anomalies and birth defects. [1]
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As of 15 December 2022 [update] :
Congress | Short title | Bill number(s) | Date introduced | Sponsor(s) | # of cosponsors | Latest status |
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115th Congress | Ensuring Lasting Smiles Act | H.R. 6689 | August 28, 2018 | Collin Peterson (D-MN) | 16 | Died in committee |
S. 3369 | August 23, 2018 | Tammy Baldwin (D-WI) | 7 | Died in committee | ||
116th Congress | Ensuring Lasting Smiles Act | H.R. 1379 | February 26, 2019 | Collin Peterson (D-MN) | 313 | Died in committee |
S. 560 | February 26, 2019 | Tammy Baldwin (D-WI) | 53 | Died in committee | ||
117th Congress | Ensuring Lasting Smiles Act | H.R. 1916 | February 2, 2021 | Anna Eshoo (D-CA) | 317 | Referred to Committees of Energy and Commerce, Ways and Means and Education and Labor. Passed the US House (310-110) on April 4, 2022. |
S. 754 | February 1, 2021 | Tammy Baldwin (D-WI) | 61 | Referred to Committee of Health, Education, Labor and Pensions |
Teratology is the study of abnormalities of physiological development in organisms during their life span. It is a sub-discipline in medical genetics which focuses on the classification of congenital abnormalities in dysmorphology. The related term developmental toxicity includes all manifestations of abnormal development that are caused by environmental insult. These may include growth retardation, delayed mental development or other congenital disorders without any structural malformations.
A birth defect, also known as a congenital disorder, is an abnormal condition that is present at birth regardless of its cause. Birth defects may result in disabilities that may be physical, intellectual, or developmental. The disabilities can range from mild to severe. Birth defects are divided into two main types: structural disorders in which problems are seen with the shape of a body part and functional disorders in which problems exist with how a body part works. Functional disorders include metabolic and degenerative disorders. Some birth defects include both structural and functional disorders.
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A congenital heart defect (CHD), also known as a congenital heart anomaly and congenital heart disease, is a defect in the structure of the heart or great vessels that is present at birth. A congenital heart defect is classed as a cardiovascular disease. Signs and symptoms depend on the specific type of defect. Symptoms can vary from none to life-threatening. When present, symptoms may include rapid breathing, bluish skin (cyanosis), poor weight gain, and feeling tired. CHD does not cause chest pain. Most congenital heart defects are not associated with other diseases. A complication of CHD is heart failure.
A ventricular septal defect (VSD) is a defect in the ventricular septum, the wall dividing the left and right ventricles of the heart. The extent of the opening may vary from pin size to complete absence of the ventricular septum, creating one common ventricle. The ventricular septum consists of an inferior muscular and superior membranous portion and is extensively innervated with conducting cardiomyocytes.
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Asymmetric crying facies (ACF), also called partial unilateral facial paresis and hypoplasia of depressor angula oris muscle, is a minor congenital anomaly caused by agenesis or hypoplasia of the depressor anguli oris muscle, one of the muscles that control the movements of the lower lip. This unilateral facial weakness is first noticed when the infant cries or smiles, affecting only one corner of the mouth and occurs on the left side in nearly 80% of cases. It is only rarely associated with other birth defects.
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A malformative syndrome is a recognizable pattern of congenital anomalies that are known or thought to be causally related.
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Constriction ring syndrome (CRS) is a congenital disorder with unknown cause. Because of the unknown cause there are many different, and sometimes incorrect names. It is a malformation due to intrauterine bands or rings that give deep grooves in, most commonly, distal extremities like fingers and toes. In rare cases the constriction ring can form around other parts of the fetus and cause amputation or even intrauterine death. The anatomy proximal to the site of constriction is developmentally normal. CRS can be associated with other malformations with club foot being most common. The precise configuration of the bands, lymphedema, and character of the amputations are not predictable and vary with each individual patient. Also more than one extremity is usually affected, and it is rare for only one ring to present as an isolated malformation with no other manifestation of this syndrome.
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The Prematurity Research Expansion and Education for Mothers who deliver Infants Early Reauthorization Act or PREEMIE Reauthorization Act is a bill that reauthorizes research programs on preterm births that are run by the Centers for Disease Control and Prevention. It also authorizes grants and demonstration programs to be run by the Health Resources and Services Administration that will try to decrease preterm births. The bill passed the United States Senate during the 113th United States Congress.
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The 117th United States Congress is the current meeting of the legislative branch of the United States federal government, composed of the United States Senate and the United States House of Representatives. It convened in Washington, D.C., on January 3, 2021, during the final weeks of Donald Trump's presidency and the first two years of Joe Biden's presidency, which will end on January 3, 2023.
Wladimir Wertelecki is a Pediatrician and Medical Geneticist who in 1974 established one of the first free-standing Departments of Medical Genetics at the new South Alabama University College of Medicine in Mobile, Alabama, U.S.A. Since 1996 and following his retirement as Chairman and Emeritus Professor of Medical Genetics, Pediatrics and Pathology, he continues his investigations of developmental anomalies and their prevention as Project Scientist at the Department of Pediatrics, University of California San Diego. Since 1996, his research focused mainly on alcohol and ionizing radiation impacts on congenital anomalies. He is the author over 135 scientific reports. In 2000, he established the OMNI-Net Ukraine Programs to investigate reproductive risks posed by exposures to alcohol and Chornobyl ionizing radiation. OMNI-Net Ukraine established a population-based registry for the epidemiological surveillance of congenital anomalies and qualified to become full member of EUROCAT, a network of over 38 such registries across Europe. OMNI-Net Ukraine is the sole full member of EUROCAT conducting such investigations in regions formerly ruled by the USSR. OMNI-Net Ukraine also implements a variety of collaborative investigations with experts from the UCSD, Emory and other Universities sponsored by the Collaborative Initiative on Fetal Alcohol Spectrum Disorders funded by then National Institute on Alcohol Abuse and Alcoholism (NIH). Many components of the OMNI-Net Ukraine programs introduced by Wertelecki, were previously implemented in Alabama. He established a regional network of clinics across southern Alabama and West Florida and in 1978 organized the Southern Genetic Group which expanded into the South-Eastern Regional Genetics Group enhancing genetic services in six states. Wertelecki also contributed to the efforts by local Native-Americans to gain Federal Recognition as Native-Americans in Alabama. In 1992, he made a presentation to the US Senate regarding the reproductive risks posed by the Chornobyl radiation. Following an initial sponsorship by USAID, he established OMNI-Net programs in Ukraine, a not-for-profit network to provide training and to engage Ukrainian professionals to conduct monitoring of the frequency of birth defects. OMNI-Net teams promptly detected an epidemic of spina bifida and associated malformations collectively known as neural tube defects (NTD). The frequency of these malformations and the associated child mortality are persistently the highest in Europe. From the start, OMNI-Net advocates for Ukrainian authorities to introduce folic acid fortification programs, a measure that will significantly reduce the epidemic and related mortality. Flour fortification with folic acid is safe, effective and affordable as shown by implementations adopted by 80 countries. Currently, a legislative initiative to establish an NTD prevention program is under consideration by the Ukrainian National Parliament. OMNI-Net has also documented that thousands of pregnant women continue to accumulate in their bodies, through eating, drinking, and inhaling, radioactive elements (nuclides). Whole body counts of incorporated Cs-137 by pregnant women are much higher than in women residing away from Chornobyl radiation impacted regions. OMNI-Net teams seek national and international partners to elucidate the inherent risks of such facts. Although some reports state that Chornobyl radiation is not biologically harmful, OMNI-Net researchers note that such studies did not include pregnant women with known levels of incorporated nuclides. The association of incorporated levels of Cs-137 with prevalence of birth defects remains to be clarified. Another frequent known cause of birth defects in Ukraine is alcohol consumption by pregnant women. Since 2006, OMNI-Net has implemented an international initiative focused on fetal alcohol spectrum disorders. In summary, OMNI-Net is effectively a catalist for joint scientific collaborations of Ukrainian and International investigations.
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This article incorporates public domain material from websites or documents of the United States Government .