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Title
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Date
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1.
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Number 550
ABSTRACT: Myelomeningocele, the most severe form of spina bifida, occurs in approximately 1 in 1,500 births in the United States. Fetuses in whom myelomeningocele is diagnosed typically are delivered...
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January 2013
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2.
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Washington, DC -- Overweight and obese women may be able to gain less than what is recommended during pregnancy and still have a healthy baby, according to new recommendations issued today by The Ame...
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December 2012
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3.
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Number 545
ABSTRACT: Noninvasive prenatal testing that uses cell free fetal DNA from the plasma of pregnant women offers tremendous potential as a screening tool for fetal aneuploidy. Cell free fetal DNA testin...
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December 2012
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4.
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FAQ060
Why is there a concern about having a child later in life?
Becoming pregnant after age 35 years can present a challenge. Also, having a child later in life has certain risks. These risks may affect ...
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December 2012
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5.
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SP060
La fertilidad
La fertilidad de todas las mujeres disminuye en cierto
grado a partir de los 30 años. Después de ese momento,
es posible que tarde más en quedar embarazada. La
fertilidad d...
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December 2012
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6.
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Washington, DC -- A new noninvasive blood test that measures cell free fetal DNA (cffDNA) to screen for three common genetic disorders early in pregnancy is extremely promising, according to a new Co...
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November 2012
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7.
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SP179
Beneficios de la prueba de detección de
portadores previa a la concepción
Puede hacerse una prueba de detección de portadores
antes del embarazo (antes de la concepción) o durante
el emb...
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August 2012
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8.
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FAQ179
What is preconception carrier screening?
Preconception carrier screening is screening that you can have before becoming pregnant to help predict your chances of having a child with a genetic disorde...
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August 2012
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9.
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August 1, 2012 — July 31, 2013
Clinical Specialists Consulting, Inc. and Perinatal University will conduct their educational activity, "abcdEFM Method-Advanced Electronic Fetal Monitoring". This web-based course will be avai...
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August 2012
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10.
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SP164
Defectos congénitos comunes
Cada año, aproximadamente 1 de cada 33 bebés nace
con un defecto congénito. Un defecto congénito es
un problema que está presente en el momento del
nacimiento...
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July 2012
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11.
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FAQ146
What is a birth defect?
A birth defect is a problem that is present at birth and affects how the baby looks, functions, or both. A birth defect also is called a congenital disorder. More than 4,000 d...
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August 2011
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12.
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FAQ165
What is a birth defect?
A birth defect is a physical problem that is present at birth. A birth defect may affect how the body looks, functions, or both. Many birth defects are mild, but some can be s...
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August 2011
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13.
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FAQ094
What are genes?
Genes control your physical makeup. Genes come in pairs. Half of a fetus's genes come from the mother. The other half comes from the father. Some traits, such as blood type, are deter...
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August 2011
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14.
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Washington, DC -- Women should be screened for alcohol use at least yearly and within the first trimester of pregnancy, according to a new Committee Opinion released today by The American College of ...
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July 2011
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15.
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Number 495
ABSTRACT: During pregnancy, severe maternal vitamin D deficiency has been associated with biochemical evidence of disordered skeletal homeostasis, congenital rickets, and fractures in the newborn. At...
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July 2011
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16.
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Number 494
Abstract: The evidence regarding an association between the nitrofuran and sulfonamide classes of antibiotics and birth defects is mixed. As with all patients, antibiotics should be prescribed for pr...
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June 2011
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17.
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Washington, DC -- In 2009, researchers from the National Birth Defects Prevention Study published a report suggesting that two types of commonly prescribed antibiotics used to treat urinary tract inf...
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May 2011
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18.
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Number 486
(Replaces No. 325, December 2005)
ABSTRACT: In 2001, the American College of Obstetricians and Gynecologists and the American College of Medical Genetics introduced guidelines for prenatal and preconception carrier screening for cyst...
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April 2011
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19.
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Number 478
ABSTRACT: Family history plays a critical role in assessing the risk of inherited medical conditions and single gene disorders. Several methods have been established to obtain family medical historie...
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March 2011
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20.
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Number 469
(Replaces No. 338, June 2006)
ABSTRACT: Fragile X syndrome is the most common inherited form of mental retardation. The syndrome occurs in approximately 1 in 3,600 males and 1 in 4,000–6,000 females. Approximately 1 in 250 female...
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October 2010
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21.
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Number 462
ABSTRACT: Moderate caffeine consumption (less than 200 mg per day) does not appear to be a major contributing factor in miscarriage or preterm birth. The relationship of caffeine to growth restrictio...
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August 2010
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22.
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Number 449
(Replaces No. 230, January 2000)
ABSTRACT: Phenylketonuria (PKU) is an autosomal recessive disorder of phenylalanine (Phe) metabolism characterized by a deficiency of the hepatic enzyme, phenylalanine hydroxylase, an enzyme responsi...
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December 2009
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23.
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Number 443
(Replaces No. 264, December 2001)
ABSTRACT: In the absence of obstetric or medical complications, pregnant women can observe the same precautions for air travel as the general population and can fly safely. Pregnant women should be i...
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October 2009
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24.
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Number 442
(Replaces No. 298, August 2004)
ABSTRACT: Certain autosomal recessive disease conditions are more prevalent in individuals of Eastern European Jewish (Ashkenazi) descent. Previously, the American College of Obstetricians and Gyneco...
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October 2009
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25.
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SP146
Los defectos congenitos afectan aproximadamente a 1 de cada 33 bebes que nacen en Estados Unidos cada ano. Aunque no es posible prevenir algunos defectos congenitos, para otros se pueden tomar medida...
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August 2009
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