Abstract |
A 21-year-old primigravida had a pregnancy complicated by hyperemesis gravidarum (HG) beginning at 7-week gestation. Despite medical therapy, she lost 18% of her prepregnancy weight. Early ultrasound at 14 weeks demonstrated a flattened facial profile with nasal hypoplasia (Binder phenotype) consistent with vitamin K deficiency from HG. She had a percutaneous endoscopic gastrojejunostomy tube placed for enteral feeding at 15-week gestation. At repeated anatomy ultrasound at 21-week gestation, delivery, and postnatal pediatric genetics exam, nasal hypoplasia was consistent with vitamin K deficiency embryopathy from HG. Nausea and vomiting of pregnancy is a common condition. HG, the most severe form, has many maternal and fetal effects. Evaluation of vitamin K status could potentially prevent this rare and disfiguring embryopathy.
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Authors | Andrew S Lane, Jennifer L Stallworth, Kacey Y Eichelberger, Kenneth F Trofatter |
Journal | Case reports in obstetrics and gynecology
(Case Rep Obstet Gynecol)
Vol. 2015
Pg. 324173
( 2015)
ISSN: 2090-6684 [Print] United States |
PMID | 26347836
(Publication Type: Journal Article)
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