I lost my baby after 12 weeks in womb. Post mortem shows baby had Eagle Barrett syndrome.? - eagle barrett syndrome
Does anyone know the cause of this and could not happen to us?
Tuesday, December 29, 2009
Eagle Barrett Syndrome I Lost My Baby After 12 Weeks In Womb. Post Mortem Shows Baby Had Eagle Barrett Syndrome.?
1 comment:
I also read this syndrome, I am truly sorry for your loss is what I found here:
Prune Belly (Eagle-Barrett) Syndrome
By Mary Kugler,
Your guide to rare diseases.
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Distinctive number of physical problems
What is it?
Prune Belly Syndrome, also known as Eagle-Barrett syndrome, triad, was born a special set of physical problems the child is. These issues are:
The abdominal muscles in the front are weak or not at all
Some parts of the urinary tract develop abnormally
) For men (95% of cases, the testes remain inside the abdomen and down not in the scrotum.
There may be other physical problems in babies, such as the curvature of the spine, hip dislocations, clubfoot, respiratory or heart problems and gastrointestinal disorders.
What are the causes?
The cause of the syndrome is unknown, but researchers believe that to develop a disruption of fetal growth, which presents problems themselves. We think that blocks some part of the fetal urinary tract, and the CauSES other parties, such as abnormal development. Prune Belly syndrome occurs in 1 in 40,000 live births in the United States
How is it diagnosed?
Ultrasound during pregnancy can sometimes find the abnormal development of the bladder and urinary tract. As the fetus develops, developed the liquid in the abdomen, the more important stretches. The liquid is absorbed before birth again, so that when the baby is born to a decrease or wrinkled abdomen (hence the "prune belly" call).
After giving birth to determine ultrasound and X-rays, the type of urinary tract abnormalities are present.
Unfortunately, the prune belly syndrome can have serious effects on the baby. 20% of children die before birth, and 30% died from kidney problems, with the first two years of life. In the remaining 50% of the children there are different degrees of urinary problems.
How is it treated?
There is no cure for the syndrome, but the repair of the urinary tract can be made. Some surgeons attempt to correct problems in the fetus before birth, but with mixed results. CH/ Children are more susceptible to urinary tract infections antibiotics. The operation can be performed on the testicles of the child to the scrotum.
Sometimes the best treatment, despite a child's kidneys no longer function (renal insufficiency). The treatment is dialysis or kidney transplantation.
Future research
Improved surgical techniques, particularly laparoscopy, is his work for a child with prune belly syndrome requires fewer repairs difficult. The more we learned about the syndrome, treatment can be improved and more children are helped to survive.
The information in this article are from source:
- Prune Belly Syndrome Network. About Prune Belly.
There is also an organization that you want to see:
For further information and assistance about rare disorders, please contact the National Organization for Rare Disorders, PO Box 1968, Danbury, CT 06813-1968, phone (203) 744-0100 or e-mail site www. @ Rarediseases rarediseases.org orphans. org
http://www.prunebelly.org /
and on the Web:
http://health.allrefer.com/health/prune- ...
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