A female infant with a 46,XX/48,XY,+8,+10 karyotype in prenatal diagnosis: a ‘vanishing twin’ phenomenon?

2001 ◽  
Vol 21 (10) ◽  
pp. 896-897 ◽  
Author(s):  
E. Lloveras ◽  
J. M. Lecumberri ◽  
C. Pérez ◽  
C. Melero ◽  
L. Zamora ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Female Infant

Congenital superior caval vein aneurysm in a newborn with cystic lymphangioma: a rare case report

2018 ◽  
Vol 28 (8) ◽  
pp. 1067-1069 ◽  
Author(s):  
Jessica Attene ◽  
Ernesto Casorelli ◽  
Paolo Versacci
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Rare Case ◽  
Neck Mass ◽  
Cystic Lymphangioma ◽  
Lymphatic Malformation ◽  
Female Infant ◽  
Caval Vein ◽  
Superior Caval Vein ◽  
Rare Case Report

AbstractDilatation of the superior caval vein is extremely rare, with few cases described among newborns. The association of aneurysm of the superior caval vein and lymphatic malformation is extremely uncommon. We report a case of a female infant with a prenatal diagnosis of superior caval vein aneurysm presenting at birth with a neck mass that was found to be a cystic lymphangioma.

A new strategy for prenatal diagnosis in a sporadic haemophilia B family

Haemophilia ◽  
2001 ◽  
Vol 7 (4) ◽  
pp. 416-418 ◽  
Author(s):  
M. Acquila ◽  
F. Bottini ◽  
A. Valetto ◽  
D. Caprino ◽  
P. G. Mori ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Haemophilia B ◽  
New Strategy

185: Does Prenatal Diagnosis Influence the Morbidity Associated with Left in Non or Poorly-Functioning Renal Moiety After Endoscopoic Puncture of Ureterocele?

2004 ◽  
Vol 171 (4S) ◽  
pp. 49-49
Author(s):  
Boris Chertin ◽  
Ron Rabinowitz ◽  
Avner Polak ◽  
Irit Hadas-Halpren ◽  
Amicur Farkas
Keyword(s):  
Prenatal Diagnosis

Purpura Fulminans in a Patient Homozygous for a Mutation in the Protein C Gene - Prenatal Diagnosis in a Subsequent Pregnancy

1996 ◽  
Vol 75 (03) ◽  
pp. 525-526 ◽  
Author(s):  
M C Alessi ◽  
M F Aillaud ◽  
O Paut ◽  
B Roquelaure ◽  
M Alhenc-Gelas ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Protein C ◽  
Purpura Fulminans ◽  
Subsequent Pregnancy

Prenatal Diagnosis of Compound Heterozygous Deficiency of Protein C by Direct Detection of the Mutation Sites

1996 ◽  
Vol 76 (02) ◽  
pp. 277-278 ◽  
Author(s):  
Masaru Ido ◽  
Tatsuya Hayashi ◽  
Junji Nishioka ◽  
Masazumi Itoh ◽  
Hiroyuki Minoura ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Protein C ◽  
Direct Detection ◽  
Compound Heterozygous ◽  
Heterozygous Deficiency
Sign in / Sign up

Export Citation Format

Share Document