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| 11. |
Dandy-Walker Malformation in a Fetus with Pentasomy X (49, XXXXX) Prenatally Diagnosed by Fluorescence in situ Hybridization Technique |
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Fetal Diagnosis and Therapy,
Volume 10,
Issue 5,
1995,
Page 333-336
Thomas D. Myles,
Laurence Burd,
Guillermo Font,
Maureen M. McCorguodale,
Donald J. McCorquodale,
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摘要:
We present the case of a pentasomy X (49, XXXXX) prenatally diagnosed. The fluorescent in situ hybridization technique assisted in making the diagnosis. The problems identified in this fetus include a Dandy-Walker malformation, hydrocephaly, ventricular septal defect, hypertelorism and polyhydramnios.
ISSN:1015-3837
DOI:10.1159/000264254
出版商:S. Karger AG
年代:1995
数据来源: Karger
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| 12. |
How to Deal with a Rare Entity: The Coexistence of a Complete Mole and a Healthy Egg in a Twin Pregnancy? |
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Fetal Diagnosis and Therapy,
Volume 10,
Issue 5,
1995,
Page 337-342
Olivier Garbin,
Romain Favre,
Philippe Weber,
Elisabeth Arbogast,
Bernard Gasser,
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摘要:
The association of a normal and a molar egg within a twin pregnancy is extremely rare. The key to diagnosis is the fetal karyotype, thus allowing elimination of its principal differential diagnosis: partial triploid mole. We report a case where the evolution of the pregnancy was complicated by severe toxemia. Interruption of pregnancy was then necessary, even though a conservative attitude had first been considered. Throughout this case, we discuss the means of diagnosis and the clinical handling of this rare entity.
ISSN:1015-3837
DOI:10.1159/000264255
出版商:S. Karger AG
年代:1995
数据来源: Karger
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| 13. |
Severe Urethral Obstruction Diagnosed at 14 Weeks’ Gestation: Variability of Outcome with and without Drainage |
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Fetal Diagnosis and Therapy,
Volume 10,
Issue 5,
1995,
Page 343-348
Robert A. MacMahon,
Peter M. Renou,
Paul A. Shekleton,
Peter J. Paterson,
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PDF (2049KB)
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摘要:
We present 3 case reports to illustrate the variability of outcome of severe fetal posterior urethral obstruction. Two of the described cases support the view that early in utero decompression of an obstructed fetal urinary system into the amniotic cavity, in the selected patient, will allow adequate lung development and will prevent the development of severe renal dysplasia. It will not prevent the abdominal wall deformity of the prune belly syndrome. The evidence suggests that to allow maximum time for lung development and to prevent increasing renal dysplasia, drainage should be performed before 18 weeks of gestation. To obtain maximum effect, this drainage should continue until at least 32-33 weeks’ gestation, so that the possible respiratory problems of prematurity would not be severe enough to compound the degree of lung hypoplasia which might be present. Case 3 supports our view that an endoscopic approach to in utero drainage of the urinary tract has the advantage of achieving drainage with minimal risk to both mother and fetu
ISSN:1015-3837
DOI:10.1159/000264256
出版商:S. Karger AG
年代:1995
数据来源: Karger
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