Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Krupa H Shah"'
Autor:
Krupa H Shah
Publikováno v:
Journal of South Asian Federation of Obstetrics and Gynaecology. 13:426-430
Publikováno v:
Turkish Journal of Obstetrics and Gynecology
Turkish Journal of Obstetrics and Gynecology, Vol 17, Iss 1, Pp 40-45 (2020)
Turkish Journal of Obstetrics and Gynecology, Vol 17, Iss 1, Pp 40-45 (2020)
Objective: First trimester aneuploidy screening (FTAS) has become an integral part of antenatal care in most of centers in India. The serum markers used for FTAS are pregnancy-associated plasma protein A (PAPP-A) and beta human chorionic gonadotropin
Publikováno v:
Journal of South Asian Federation of Obstetrics and Gynaecology. 11:185-189
Publikováno v:
International Journal of Infertility & Fetal Medicine. 8:89-92
Congenital pulmonary airway malformation (CPAM) is a rare developmental lung abnormality. It is also referred as a congenital cystic adenomatoid malformation. The exact etiology is not known yet. The majority of cases are detected during targeted pre
Publikováno v:
Congenital Anomalies. 56:119-126
Urorectal septum malformation sequence (URSMS) is a rare spectrum of malformations involving various organ systems. Here, we present eight cases of URSMS, noted in autopsy, with different degrees of complexity, seven being the complete type and one b
Publikováno v:
Journal of Family Medicine and Primary Care
Journal of Family Medicine and Primary Care, Vol 7, Iss 2, Pp 458-460 (2018)
Journal of Family Medicine and Primary Care, Vol 7, Iss 2, Pp 458-460 (2018)
Fetal intra-abdominal umbilical vein varix (FIUVV) is a rare pathology and suggests an enlargement of the umbilical vein. Prenatal diagnosis is done through meticulous ultrasound imaging. Management variables are the diameter of varix, presence or ab
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 7, Pp QD08-QD09 (2018)
Nephrotic Syndrome (NS), a unique renal disease complex associated with heavy proteinuria (protein excretion >3.5 gm/day), hypoalbuminemia (
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 10, Pp QE01-QE05 (2018)
Recurrent Pregnancy Loss (RPL) is an important reproductive issue, affecting 1-5% of couples. It is characterised by repeated miscarriage, impairing the ability to have a live birth. The proven causes are diverse, such as cytogenetic abnormality, ute
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 9, Pp QC10-QC13 (2018)
Introduction: Routinely performed aneuploidy screen takes into account free beta human chorionic gonadotrophins (β-hCG), Pregnancy Associated Plasma Protein-A (PAPP-A), nuchal translucency, and various maternal characteristics. Incidental finding of
Publikováno v:
JBJS case connector. 7(2)
Case: We report a unique combination of neonatal bilateral proximal femoral focal deficiency with a congenital tibiofemoral fusion of the right leg. Conclusion: To the best of our knowledge, the combination of proximal femoral focal deficiency and th