Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Linnie M. Muller"'
Publikováno v:
American Journal of Medical Genetics. 75:283-287
We describe the antenatal ultrasound findings of growth retardation, oligohydramnios, mesomelic limb shortness, and cardiac, renal, and hand defects in a fetus who was postnatally diagnosed as having RSH ("Smith-Lemli-Opitz") syndrome. An unusual fin
Publikováno v:
American Journal of Medical Genetics. 25:119-129
The prenatal ultrasonographic features found in two cases each of the Pena-Shokeir I and the trisomy 18 syndromes are described. All four cases were referred for ultrasonographic evaluation of polyhydramnios, clinically detected in the third trimeste
Autor:
Linnie M. Muller, S. C. E. Mouton, H. F. Jordaan, James F. Reynolds, Greetje de Jong, Patricia A. Kirby, Richard H. Hewlett, M. J. Greeff
Publikováno v:
American Journal of Medical Genetics. 26:421-429
A diagnosis of the Neu-Laxova syndrome was made by ultrasonography in the third trimester of pregnancy. Initial ultrasonographic examination, at approximately 28 wk gestation, showed intrauterine growth retardation (IUGR), hypoechoic skeletal structu