We report on prenatal and postnatal findings in 4 consecutive fetuses with a pattern of severe congenital anomalies who were born to a healthy nonconsanguineous couple. The spectrum of malformations includes diaphragmatic defects, hypoplastic lungs, omphalocele, limb deficiencies, syndactyly of toes
β¦ LIBER β¦
Ocular malformations, moyamoya disease, and midline cranial defects: a distinct syndrome
β Scribed by Sophie J. Bakri; Daniel Siker; Thomas Masaryk; Mark G. Luciano; Elias I. Traboulsi
- Book ID
- 117019908
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 304 KB
- Volume
- 127
- Category
- Article
- ISSN
- 0002-9394
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Diaphragmatic defects, limb deficiencies
β
Froster, Ursula G.; Kolditz, Petra; Wisser, Josef; Robbiani, Mario B.; Stallmach
π
Article
π
1996
π
John Wiley and Sons
π
English
β 34 KB
π 2 views
Postnatal growth retardation, facial dys
β
SΓ©rgio B. Sousa; GeneviΓ©ve Baujat; VΓ©ronique Abadie; Damien Bonnet; Daniel Sidi;
π
Article
π
2010
π
John Wiley and Sons
π
English
β 246 KB
π 2 views
Two siblings with midline field defects
β
Jespers, A. ;Buntinx, I. ;Melis, K. ;Vaerenberg, M. ;Janssens, G.
π
Article
π
1993
π
John Wiley and Sons
π
English
β 382 KB
π 3 views
We describe 2 sibs with multiple congenital anomalies. The main manifestations include hypoplasia of the corpus callosum and/or cerebellar hypoplasia, Robin sequence, pharyngeal and laryngeal hypoplasia, abnormal ears, excessive neck skin, cardiac defect, and Hirschsprung disease. The presence in 2