Holoprosencephaly And Patau Syndrome
"Holoprosencephaly is a group of disorders characterized by failure of diverticulation and cleavage of prosencephalon at the rostral end of primitive neural tube and hypoplasia or aplasia of premaxillary segment of face. Incidence of holoprosencephaly is 6-12 /1000 live birth and 40/1000 in embryos with recurrence rate of 6% for non chromosomal form and 13% for autosomal dominant form. It is most frequently seen in trisomy 13 &18 and can be caused by teratogen as in infant of diabetic mother."
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Holoprosencephaly And Patau Syndrome
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Reviewed by Sumer Sethi
on
Wednesday, November 08, 2006
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Sumer Sethi
Unique blend of academic excellence and entrepreneurship, heading leading firms in India- Teleradiology Providers, pioneering company providing teleradiology services and DAMS (Delhi Academy of Medical Sciences) Premier test preparation institute in India for MD/MS/MCI preparation. He has also been an invited faculty member at various conferences, including Teleradiology in IRIA 2008 and 2011, Hospital Build Middle East, Congress of the Brain Tumor Radiology in Neuro-oncology Society. Dr. Sethi is Editor-in-Chief of Internet Journal of Radiology. He has a keen interest in Web 2.0 technologies and in maintaining his famous radiology blog, which has been featured in multiple international journals.
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Patau Syndrome Survivors and those who were carried to term.
Living with Trisomy 13 - Patau syndrome
http://www.livingwithtrisomy13.org
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