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Fetal alcohol spectrum disorders encompass a range of physical and neurodevelopmental problems which can result from prenatal alcohol exposure. Diagnosis is based on the signs and symptoms in the person and evidence of alcohol use. [1] These diagnoses of fetal alcohol spectrum disorders are currently recognized: Fetal alcohol syndrome (FAS) [1]
Microcephaly (from Neo-Latin microcephalia, from Ancient Greek μικρός mikrós "small" and κεφαλή kephalé "head" [2]) is a medical condition involving a smaller-than-normal head. [3] Microcephaly may be present at birth or it may develop in the first few years of life. [ 3 ]
Maxillary hypoplasia can be present as part of genetic syndromes such as Angelman syndrome. Fetal alcohol syndrome is associated with maxillary hypoplasia. Injury to facial bones during childhood can lead to atypical growth. Exposure to Phenytoin in the first trimester of pregnancy has also been associated with the development of maxillary ...
At least 10 babies — possibly more than 12 — have been identified with what doctors believe to be a new syndrome related to exposure to fentanyl in the womb.. All of the infants have ...
TALLAHASSEE — Pointing to a “medical consensus” about Fetal Alcohol Syndrome, attorneys for inmate Michael Duane Zack on Sunday urged the Florida Supreme Court to block his scheduled Oct. 3 ...
People with fetal alcohol spectrum disorder. Pages in category "People with fetal alcohol spectrum disorder" The following 10 pages are in this category, out of 10 total.
Fetal Alcohol Syndrome has numerous symptoms which may include cognitive impairments and impairment of the facial features. [43] PAE remains the leading cause of birth defects and neurodevelopmental abnormalities in the United States, affecting 9.1 to 50 per 1000 live births in the U.S. and 68.0 to 89.2 per 1000 in populations with high levels ...
It is often a result of fetal alcohol syndrome (FAS), caused by large alcohol intake in the first month of pregnancy. [citation needed] It can be associated with trisomy 13, which is also known as Patau syndrome, [3] as well as hereditary neuralgic amyotrophy. [4] It can also be associated with fragile X syndrome and Prader–Willi syndrome.