Zobrazeno 1 - 9
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pro vyhledávání: '"Meetan Preet"'
Publikováno v:
Fetal and Pediatric Pathology. 41:837-842
Background Congenital muscular dystrophies (CMD) range in phenotype from an antenatal presentation with brain and eye anomalies to isolated muscular weakness. B4GAT1 gene has recently been associated with muscular dystrophy-dystroglycanopathy, type A
Publikováno v:
Journal of Fetal Medicine. :27-30
Congenital absence of aortic valve cusps is a rare congenital heart malformation, which is commonly associated with other cardiac defects. Isolated absence of aortic valve or one leaflet is extremely rare and has not been described antenatally. We pr
Publikováno v:
Journal of Fetal Medicine. :47-49
We report a case of caudal regression syndrome in a 31-year-old primigravida having type-1 diabetes mellitus for the past eight years who was referred to our institution for a first trimester sonogram. Prenatal ultrasound examination revealed a crown
Publikováno v:
Journal of Fetal Medicine. :37-39
Tetra-amelia is characterized by the absence of all four limbs. It is a rare congenital anomaly, with an incidence of 1.5–4 per 100,000 births. It occurs as a result of developmental interruption between 24th and 36th days after fertilization. Its
Publikováno v:
Journal of Fetal Medicine. :161-165
The objective of the present study was to investigate the effectiveness of a simplified approach by using two dimensional (2D) technique for evaluation of the midline structures of the fetal brain and comparing it with the three dimensional (3D) tech
Publikováno v:
Journal of Fetal Medicine; December 2015, Vol. 2 Issue: 4 p161-165, 5p
Publikováno v:
Journal of Fetal Medicine; December 2017, Vol. 4 Issue: 4 p203-205, 3p
Publikováno v:
Journal of Fetal Medicine; March 2017, Vol. 4 Issue: 1 p37-39, 3p
Publikováno v:
Journal of Fetal Medicine; March 2017, Vol. 4 Issue: 1 p47-49, 3p