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| | USDSM Birth Defects Genetics Center Home Page |
 | | Under the section on genetic screening are fourteen items that need to be recorded: parental age, ethnicity, history of birth defects such as neural tube defects, Down syndrome, sickle cell anemia, muscular dystrophy, hemophilia, cystic fibrosis, Huntington chorea, mental retardation or other inherited disorders, medications or street drugs. |
 | | It is, therefore, prudent to seek chromosome studies of the affected child in the family for verification of translocation versus nondisjunction as the causative mechanism for the Down syndrome. |
 | | For male factor infertility, genetic conditions such as cystic fibrosis may result in congenital absence of the vas deferens; myotonic dystrophy with associated recession of frontal hairline, testicular atrophy, and other associated symptoms of myotonia; Klinefelter syndrome or deficient masculinization (XXY or various XY/XX or XO mosaicism). |
| www.usd.edu /med/genetics/preconceptualcounseling.htm (3491 words) |
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