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Communication for the Heartland Regional Genetics Group

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Subject:	fetal demise with anomalies
From:	"Troxell, Robin M." <[log in to unmask]>
Reply To:	Communication for the Heartland Regional Genetics Group <[log in to unmask]>
Date:	Mon, 19 Feb 2007 13:08:50 -0600
Content-Type:	text/plain
Parts/Attachments:	text/plain (14 lines)

Hello -
I have a 23 year old G2,P1,IUFD1 patient returning for counseling this week.  Baby had severe hydrops/anasarca, single-chamber heart, cystic kidneys with probably hydronephrosis, IUGR, cystic hygroma, dilated 4th ventricle of brain, and bilateral cervical/?branchial cleft cysts first noted on 20 week scan.  Autopsy at 22 weeks after demise was limited to gross exam which was normal, except for ambiguous genitalia.  Parents were told baby was male.  Karyo 46,XX.  No samples from baby remaining.  Anything specific to offer them at this point?
 
Thanks,
Robin
************************************
Robin M. Troxell, MS, CGC
Genetic Counselor
University of Missouri Department of Child Health
Mercy St. John's Hospital (Springfield, MO)
(p) 417-820-9839
(f) 417-820-3720
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