Defects » Other
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A 12 month review of small heads & small legs - are we over investigating?
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A case lymphoma of the uterine cervix
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A case of ex utero intrapartum treatment in a rare craniofacial tumor
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A case of fatal complex umbilical cord anomaly
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A case of first trimester ultrasonographic approach to diagnosing Sirenomelia
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A case of from suspected clubfoot to multiple pterygium syndrome
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A case of giant fetal sacrococcygeal teratoma
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A case of integral study in a patient with sonographic appearance of hydropic degeneration in ultrasound
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A case of klippel -Trenaunay syndrome associated with large splenic cystic lymphangioma and pregnancy
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A case of massive neck fetal lymphangioma
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A case of prenatal ultrasonographic diagnosis of umbilical vein varix at 36 weeks and management
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A case of unraveling the ganglionic eminence anomalies in monozygotic twin pregnancy
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A case reprot caudal regression syndrome
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A case study on Type 2 sacrococcygeal teratoma (SCT)
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A clinical perspective on cystic placental changes: insights from three unique cases
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A paradigm shift: diagnosing fetal malformations on the 1st trimester ultrasound
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A rare case of midline developmental defect in fetal period
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Abnormal digestive images: ultrasonographic aspects and diagnoses
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Agenesis of the ductus venosus – three cases with favorable evolution
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Chorioangioma: an unusual prenatal diagnosis
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Clinical case of antenatally diagnosed sirenomelia
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Cord cyst, the first sign of a polymalformative syndrom
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Discrepancy in menstrual and ultrasound-based gestational age is associated with chromosomal aberrations and adverse pregnancy outcomes
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Feasibility and limitations of the prenatal sonographic assessment of choanal flow
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Fetal hydrops - mediastinal teratoma
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Fetal hydrops in the third trimester in a case with RASA1 mutation and Parkes-Weber syndrome
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First trimester diagnosis of Cystic Hygromas: presentetion of fetal lymphangioma in association with chromosomal aberrations
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Fraser Syndrome with Limb Reduction Defect: a rare and unique anatomic variation
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From the phenotype to the genotype: Apert syndrome
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Ichthyosis fetalis - prenatal ultrasound and molecular diagnosis and postnatal course
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IMITAS: National implementation of first-trimester anomaly scan in The Netherlands
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Low PAPP-A (<0.3MoM) at first trimester screening and structural abnormalities in euploid fetuses
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Missed anomalies on second trimester ultrasound in a low-risk population
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Partial hydatidiform mole in the second trimester
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Pattern of major congenital anomalies in Brazil: a study from 2011 to 2020
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Perinatal thoraco-abdominal tumors management in infants: a multicenter experience
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Placenta percreta invading the urinary bladder
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Predicting cognitive and developmental disorders using deep learning
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Prenatal diagnosis of generalized arterial calcification of infancy (GACI) in two Indian families
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Report of births due to Congenital Anomalies in the most complex Pediatric Hospital of CABA, Argentina
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Results of 6 cases with ductus venosus agenesis in 7846 screened pregnancies. The role of exome sequencing
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Size of the fetal thymus according to the amniocentesis indication in the State Center for Timely Prenatal Screening in Mexico
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Terminal meningomyelocele vs sacrococcygeal teratoma: searching a second opinion
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The impact of first-trimester ultrasound on the early detection of fetal morphological anomalies (1994-2020)