2005
DOI: 10.1002/pd.1103
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Placental mesenchymal dysplasia associated with fetal aneuploidy

Abstract: Molar ultrasonographic appearances associated with increased maternal serum alpha-fetoprotein but normal, or slightly elevated, levels of ss human Chorionic Gonadotrophin should raise the clinical suspicion of PMD. The diagnosis of this condition should not be disregarded when an abnormal fetus and/or an abnormal karyotype are demonstrated.

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Cited by 93 publications
(91 citation statements)
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“…Another characteristic feature of PMD is aneurismal and varicose dilation of fetal chorionic vessels. Of the 110 cases reviewed, 48 cases of PMD presented data of dilation of fetal chorionic vessels [2,3,9,11,12,13,14,15,17,18,20,21,22,23,24,26,34,35,36,40,41,44,45,46,47,48]. Figure 6 represents the gestational age when aneurismal and varicose dilation of chorionic vessels were identified in the 48 cases and the current case.…”
Section: Resultsmentioning
confidence: 99%
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“…Another characteristic feature of PMD is aneurismal and varicose dilation of fetal chorionic vessels. Of the 110 cases reviewed, 48 cases of PMD presented data of dilation of fetal chorionic vessels [2,3,9,11,12,13,14,15,17,18,20,21,22,23,24,26,34,35,36,40,41,44,45,46,47,48]. Figure 6 represents the gestational age when aneurismal and varicose dilation of chorionic vessels were identified in the 48 cases and the current case.…”
Section: Resultsmentioning
confidence: 99%
“…Of the 110 cases reviewed, 16 (14.5%) were associated with BWS [2,3,4,5,6,7,8,9,10], 33 (30.0%) had evidence of fetal growth restriction [4,11,12,13,14,15,16,17,18,19,20,21,22,23,24,41,46,48] as in the current case, and 28 (25.5%) ended in intrauterine fetal death [4,6,7,8,12,13,15,16,17,18,25,26,45,47]. There is a female preponderance in cases of PMD; of the infant data reviewed, there were 78 females and 19 males.…”
Section: Resultsmentioning
confidence: 99%
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“…Las comunicaciones previas indicaron constitución genética biparental normal (11,14) . Sin embargo, recientemente, Cohen y col. (26) describieron 3 casos con aneuplodías: una trisomía 13 con translocación balanceada entre los cromosomas 1 y 13, un síndrome de Klinefelter (47,XXY) y una triplodia (69,XXX; un caso previamente informado por Paradinas y col. (16) ). Es posible que estas raras aneuploidias sean coincidencias.…”
Section: Discussionunclassified