Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Calvin E. Oyer"'
Publikováno v:
Cardiovascular Pathology. 9:39-47
Premature closure of the ductus arteriosus (PCDA) is an uncommon defect in which pulmonary hypertension (PH) has been documented by echocardiography in patients and by direct measurement after experimental PCDA in animals. The pulmonary vascular hist
Publikováno v:
Pediatric and Developmental Pathology. 2:215-220
In fetuses and neonates hepatic subcapsular hematomas are relatively common lesions and may be life-threatening. Conditions previously associated with these hematomas include trauma, coagulopathies, hypoxia, sepsis, pneumothorax, maternal diseases, a
Publikováno v:
Pediatric and Developmental Pathology. 1:433-437
We report a neonate with neonatal hemochromatosis (NH), renal tubular dysgenesis (RTD), and hypocalvaria. NH is a fatal condition of the newborn, characterized by severe idiopathic liver failure of intrauterine onset and siderosis, intra- and extrahe
Publikováno v:
Pediatric and Developmental Pathology. 1:314-318
Cleidocranial dysplasia (CCD), an uncommon disorder involving membranous bones, is rarely lethal in early life. The calvaria is defective and wormian bones are present. Abnormalities of the clavicles vary in severity from a minor unilateral defect to
Publikováno v:
Prenatal Diagnosis. 16:431-435
The objective was to investigate whether non-immune hydrops in euploid pregnancies is associated with alterations in the second-trimester levels of maternal serum alpha-fetoprotein (AFP), unconjugated oestriol (uE3), and human chorionic gonadotropin
Publikováno v:
American Journal of Medical Genetics. 59:295-299
Autopsy records from the Women and Infants' Hospital from January 1974 through January 1994 were reviewed to identify cardiac malformations in the presence of skeletal dysplasia. Of 24 cases of lethal fetal or neonatal osteochondrodysplasias, 4 were
Autor:
Siegfried M. Pueschel, Calvin E. Oyer
Publikováno v:
Child's Nervous System. 11:639-642
An infant with Zellweger syndrome is reported. A detailed description of the clinical findings is provided. In particular, the neuropathological aspects are highlighted and the underlying biochemical derangements discussed. In addition, some of the k
Publikováno v:
Pediatric Cardiology. 16:95-99
Congenital heart disease occurs in 35-50% of patients diagnosed with Noonan syndrome. We present an infant with an unusual combination of congenital heart defects not previously reported, including partial atrioventricular septal defect, polyvalvular
Publikováno v:
Pediatric Pathology. 13:381-386
This study evaluates the practical utility of the polymerase chain reaction (PCR) as a diagnostic method for intrauterine fetal parvovirus infection in cases of hydrops fetalis. Paraffin-embedded, formalin-fixed fetal tissues from cases of hydrops fe
Publikováno v:
Human Pathology. 31:1433-1435