Výsledky vyhledávání - "J P, Schaaps"

Autor: A, Verloes, F, Narcy, B, Grattagliano, A L, Delezoide, P, Guibaud, J P, Schaaps, M, Le Merrer, P, Maroteaux

Publikováno v: Journal of Medical Genetics. 31:772-778

We report a multiple congenital anomalies (MCA) syndrome in three unrelated fetuses consisting of extremely thin, dense, fishbone-like diaphyses, flared metaphyses, mild micromelic dwarfism, brachydactyly, facial dysmorphism, ocular malformations (mi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb924306706ee209eb6aaabc8f944d14
https://doi.org/10.1136/jmg.31.10.772

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[Clinical case of the month. Unfavourable outcome of a triplet gestation]

Autor: X, Capelle, J-V, Bavi, J-P, Schaaps, F, Kridelka, J-M, Foidart

Publikováno v: Revue medicale de Liege. 66(9)

Body stalk anomaly is rarely described in triplet gestation after medically assisted procreation. The relationship between congenital anomaly, multiple pregnancy, and medically assisted procreation is briefly discussed.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fbdc5d3a9f41b6c3a376914cf281e8d3
https://pubmed.ncbi.nlm.nih.gov/21995234

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[X-linked hydrocephaly. A case report in fetal medicine]

Autor: K, Syrios, K, Delbecoue, S, Gaillez, J P, Schaaps, F, Chantraine

Publikováno v: Revue medicale de Liege. 66(3)

X-linked hydrocephaly (Li Syndrome) is a rare cause of hydrocephaly. It is, however, the most common genetic form of congenital hydrocephaly and consists of the association of hydrocephaly, mental retardation, leg spasticity and adducted thumbs. The

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7b7bfcfc26571361f0277be96666208a
https://pubmed.ncbi.nlm.nih.gov/21560427

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[Predictive value of antenatal ultrasound for the neonatal diagnostic of renal and ureteral anomaly]

Autor: F, Loumaye, E, de Gottal, J P, Schaaps, J M, Foidart

Publikováno v: Revue medicale de Liege. 63(12)

Pyelectasis is a dilatation of the renal pelvis. It must be differentiated from hydronephrosis which is a dilation of the renal pelvis and of the renal calyces. In this retrospective study, we focused on the treatment and follow up of 31 newborns in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3fae18484d163c34afb1b4e196f5caf2
https://pubmed.ncbi.nlm.nih.gov/19180834

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[How I explore...the benefit of 3D/4D ultrasound in obstetrics]

Autor: F, Chantraine, J P, Schaaps, J M, Foidart

Publikováno v: Revue medicale de Liege. 63(3)

During recent years, 3D has become an important tool in ultrasound. In obstetrics, the classic 2D examination with Doppler is now often completed by 3D. In this article the strengths and weaknesses of this technique are discussed.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9eb35228e64b4f6729d459ccbe89f28f
https://pubmed.ncbi.nlm.nih.gov/18561772

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[New methods of prenatal screening for trisomy 21]

Autor: X, Capelle, J P, Schaaps, J M, Foidart

Publikováno v: Revue medicale de Liege. 63(2)

Down syndrome is the most commonly recognized genetic cause of mental retardation. The risk of trisomy 21 is directly related to maternal age which can be viewed as the first screening test in the 1970's. New strategies for Down syndrom, have emerged

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ee3c2797932dc7ad5aae6663a042925c
https://pubmed.ncbi.nlm.nih.gov/18372545

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[A rare case of placental chorioangioma associated with neonatal disseminated hemangiomatosis]

Autor: X, Capelle, P, Syrios, F, Chantraine, V, Rigo, J-P, Schaaps, F, Kridelka, J-M, Foidart

Publikováno v: Journal de gynecologie, obstetrique et biologie de la reproduction. 38(3)

Placental chorioangioma is a benign vascular tumor. Lesions larger than 4 cm may cause fetal and maternal complications. Its association with disseminated neonatal hemangiomatosis is rarely described. We report a case of a large chorioangioma associa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c2feb5294dd522fffba30723c123816d
https://pubmed.ncbi.nlm.nih.gov/19303223

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[Fetal RHD in maternal plasma in prenatal follow-up]

Autor: J F, Dricot, J M, Minon, J P, Schaaps, P, Dewez, J M, Foidart

Publikováno v: Revue medicale de Liege. 61(12)

Since the beginning of RHD genotyping in maternal plasma, no Rh D positive baby was diagnosed RHD negative in our institution. Genotyping from circulating DNA in maternal plasma is as efficient as genotyping on amniocyts but without the associated ri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::29de34b66df55649449ace7149666792
https://pubmed.ncbi.nlm.nih.gov/17313118

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[New approaches to prenatal diagnosis of rhesus incompatibility]

Autor: J M, Minon, C, Gérard, J F, Dricot, C, Neve, J M, Senterre, J P, Schaaps, J M, Foidart

Publikováno v: Revue medicale de Liege. 61(11)

Despite generalisation of anti-D immunoprophylaxis, RhD allo-immunisation still remains the major cause of severe haemolytic disease of the fetus and of the newborn (HDFN). The routine follow up of pregnant women comprises: the ABO/D, Rh/Kell red cel

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::65b5bd795da1a0d8ac7a03d4aa2dfb75
https://pubmed.ncbi.nlm.nih.gov/17191743

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