Respiratory syncytial virus is an important pathogen responsible for lower respiratory tract infections in neonates. This study describes the epidemiological and clinical profile of RSV-positive BAV in 7 newborns who ...Respiratory syncytial virus is an important pathogen responsible for lower respiratory tract infections in neonates. This study describes the epidemiological and clinical profile of RSV-positive BAV in 7 newborns who tested positive using PCR-triplex at the neonatology and neonatal intensive care department at Mohammed VI University Hospital-OUJDA (MOROCCO) during the winter of 2024. Among the subjects of our study, there was a female predominance. 29% of cases presented with congenital heart disease, 43% presented with urinary co-infection and 14% died. The average duration of hospitalization was 9 days.展开更多
Maternal diabetes during pregnancy carries potential risks for both the mother and the developing fetus. The objective of this investigation was to evaluate the morbidity and mortality outcomes among infants born to m...Maternal diabetes during pregnancy carries potential risks for both the mother and the developing fetus. The objective of this investigation was to evaluate the morbidity and mortality outcomes among infants born to mothers with diabetes, and to determine the key maternal and neonatal risk factors associated with these outcomes. This was a retrospective, observational study designed to provide a descriptive and analytical assessment of the data, conducted over a one-year period in the Neonatology and Neonatal Intensive Care Unit of CHU MED VI in Oujda, between January 1, 2023, and December 31, 2023. The results showed a prevalence of 11.23%. The parturients had a history of abortion, preeclampsia and intra uterine fetal death. The sex ratio was 1.81, with an average weight of 3302 g. Respiratory distress was the most common complication followed by prematurity, macrosomia and congenital malformations. Uncontrolled diabetes was associated with serious neonatal complications, as well as advanced maternal age and grand multiparity. The findings underscore the necessity of providing specialized care and close monitoring for newborns born to mothers with diabetes, along with a multidisciplinary care model to address the management of any neonatal complications that may arise.展开更多
Potter syndrome is a rare congenital malformation that primarily affects male fetuses;it is characterized by pulmonary hypoplasia, skeletal malformation, and kidney abnormalities. The pressure of the uterine wall due ...Potter syndrome is a rare congenital malformation that primarily affects male fetuses;it is characterized by pulmonary hypoplasia, skeletal malformation, and kidney abnormalities. The pressure of the uterine wall due to oligohydramnios leads to an unusual facial appearance, abnormal limbs in abnormal positions, or contractures. The fetus generally dies soon after birth due to respiratory insufficiency. The baby was a live preterm male, born to a 30-year-old multigravida, out of a non-consanguineous marriage via cesarean section. There was no liquor at the time of delivery. The baby did not cry immediately after birth and required resuscitation, followed by mechanical ventilation. Multiple congenital anomalies suggestive of Potter’s syndrome were noted including facial features, flattened nose, low protruding ear, retrognathism, and epicanthal folds with unilateral atresia of the choana. Chest X-ray showed small volume lung fields suggestive of pulmonary hypoplasia, and we had on ultrasonography bilateral polycystic kidney disease on ultrasonography. At 42 hours of life, the baby developed tachypnea and severe chest retractions and died due to respiratory insufficiency. Our case highlights the importance of regular prenatal checks and examinations in each pregnancy, which helps to collect suspected cases and improve knowledge of this syndrome for better management.展开更多
Salmonella meningitis is an uncommon condition in neonates, and when it does occur, it is often linked to serious complications, such as subdural collections and abscesses. We present a case involving a 23-day-old neo...Salmonella meningitis is an uncommon condition in neonates, and when it does occur, it is often linked to serious complications, such as subdural collections and abscesses. We present a case involving a 23-day-old neonate diagnosed with Salmonella meningitis, who developed complications including bilateral intra-parenchymal hematomas with ventricular involvement. The infant showed significant improvement following an extended course of systemic antibiotics and supportive care.展开更多
Fraser syndrome is a rare malformative genetic syndrome whose main manifestations are cryptophthalmia, syndactyly, laryngeal atresia and urogenital malformations. We report the observation of a newborn from a non-cons...Fraser syndrome is a rare malformative genetic syndrome whose main manifestations are cryptophthalmia, syndactyly, laryngeal atresia and urogenital malformations. We report the observation of a newborn from a non-consanguineous marriage, admitted to the neonatology and neonatal intensive care unit at Day 1 of life for a poly-malformative syndrome. Clinically, the newborn presented with bilateral anophthalmia, cleft palate, dysmorphic facies with a rounded forehead, hypertelorism, micrognathia, low-set ears and a short neck, syndactility and bilateral cryptorchidism. Trans fontanellar ultrasound revealed tri ventricular hydrocephalus. Cerebral MRI angiography showed malformative tri-ventricular hydrocephalus, hypoplasia of the brainstem and cerebellum, and poly-microgyria. Transthoracic and renal ultrasonography were unremarkable, and the chest X-ray was normal. The authors discuss the malformative clinical and para-clinical aspects of this syndrome, multidisciplinary management and the importance of prenatal diagnosis.展开更多
<strong>Introduction</strong><span style="font-family:Verdana;"><strong>:</strong> The</span><span style="font-family:Verdana;"> </span><span styl...<strong>Introduction</strong><span style="font-family:Verdana;"><strong>:</strong> The</span><span style="font-family:Verdana;"> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">aorto-pulmonary window is a rare congenital heart disease. It is a defect between the ascending aorta and the trunk of the pulmonary artery upstream of the pulmonary bifurcation. Once the diagnosis is made, surgery must be performed quickly to avoid progression to pulmonary arteriolitis. We report the case of a 4-month-old infant in whom we made the diagnosis of aorto-pulmonary window type I. He was able to benefit from an open heart surgery at FES with an excellent result after closing the window. </span><b><span style="font-family:Verdana;">Conclusion</span></b><span style="font-family:Verdana;">: The</span></span><span style="font-family:Verdana;"> </span><span style="font-family:Verdana;">aorto-pulmonary window is a rare congenital heart defect, the diagnosis of which must be made as early as possible in order to avoid the progression to pulmonary hypetension and heart failure.</span>展开更多
文摘Respiratory syncytial virus is an important pathogen responsible for lower respiratory tract infections in neonates. This study describes the epidemiological and clinical profile of RSV-positive BAV in 7 newborns who tested positive using PCR-triplex at the neonatology and neonatal intensive care department at Mohammed VI University Hospital-OUJDA (MOROCCO) during the winter of 2024. Among the subjects of our study, there was a female predominance. 29% of cases presented with congenital heart disease, 43% presented with urinary co-infection and 14% died. The average duration of hospitalization was 9 days.
文摘Maternal diabetes during pregnancy carries potential risks for both the mother and the developing fetus. The objective of this investigation was to evaluate the morbidity and mortality outcomes among infants born to mothers with diabetes, and to determine the key maternal and neonatal risk factors associated with these outcomes. This was a retrospective, observational study designed to provide a descriptive and analytical assessment of the data, conducted over a one-year period in the Neonatology and Neonatal Intensive Care Unit of CHU MED VI in Oujda, between January 1, 2023, and December 31, 2023. The results showed a prevalence of 11.23%. The parturients had a history of abortion, preeclampsia and intra uterine fetal death. The sex ratio was 1.81, with an average weight of 3302 g. Respiratory distress was the most common complication followed by prematurity, macrosomia and congenital malformations. Uncontrolled diabetes was associated with serious neonatal complications, as well as advanced maternal age and grand multiparity. The findings underscore the necessity of providing specialized care and close monitoring for newborns born to mothers with diabetes, along with a multidisciplinary care model to address the management of any neonatal complications that may arise.
文摘Potter syndrome is a rare congenital malformation that primarily affects male fetuses;it is characterized by pulmonary hypoplasia, skeletal malformation, and kidney abnormalities. The pressure of the uterine wall due to oligohydramnios leads to an unusual facial appearance, abnormal limbs in abnormal positions, or contractures. The fetus generally dies soon after birth due to respiratory insufficiency. The baby was a live preterm male, born to a 30-year-old multigravida, out of a non-consanguineous marriage via cesarean section. There was no liquor at the time of delivery. The baby did not cry immediately after birth and required resuscitation, followed by mechanical ventilation. Multiple congenital anomalies suggestive of Potter’s syndrome were noted including facial features, flattened nose, low protruding ear, retrognathism, and epicanthal folds with unilateral atresia of the choana. Chest X-ray showed small volume lung fields suggestive of pulmonary hypoplasia, and we had on ultrasonography bilateral polycystic kidney disease on ultrasonography. At 42 hours of life, the baby developed tachypnea and severe chest retractions and died due to respiratory insufficiency. Our case highlights the importance of regular prenatal checks and examinations in each pregnancy, which helps to collect suspected cases and improve knowledge of this syndrome for better management.
文摘Salmonella meningitis is an uncommon condition in neonates, and when it does occur, it is often linked to serious complications, such as subdural collections and abscesses. We present a case involving a 23-day-old neonate diagnosed with Salmonella meningitis, who developed complications including bilateral intra-parenchymal hematomas with ventricular involvement. The infant showed significant improvement following an extended course of systemic antibiotics and supportive care.
文摘Fraser syndrome is a rare malformative genetic syndrome whose main manifestations are cryptophthalmia, syndactyly, laryngeal atresia and urogenital malformations. We report the observation of a newborn from a non-consanguineous marriage, admitted to the neonatology and neonatal intensive care unit at Day 1 of life for a poly-malformative syndrome. Clinically, the newborn presented with bilateral anophthalmia, cleft palate, dysmorphic facies with a rounded forehead, hypertelorism, micrognathia, low-set ears and a short neck, syndactility and bilateral cryptorchidism. Trans fontanellar ultrasound revealed tri ventricular hydrocephalus. Cerebral MRI angiography showed malformative tri-ventricular hydrocephalus, hypoplasia of the brainstem and cerebellum, and poly-microgyria. Transthoracic and renal ultrasonography were unremarkable, and the chest X-ray was normal. The authors discuss the malformative clinical and para-clinical aspects of this syndrome, multidisciplinary management and the importance of prenatal diagnosis.
文摘<strong>Introduction</strong><span style="font-family:Verdana;"><strong>:</strong> The</span><span style="font-family:Verdana;"> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">aorto-pulmonary window is a rare congenital heart disease. It is a defect between the ascending aorta and the trunk of the pulmonary artery upstream of the pulmonary bifurcation. Once the diagnosis is made, surgery must be performed quickly to avoid progression to pulmonary arteriolitis. We report the case of a 4-month-old infant in whom we made the diagnosis of aorto-pulmonary window type I. He was able to benefit from an open heart surgery at FES with an excellent result after closing the window. </span><b><span style="font-family:Verdana;">Conclusion</span></b><span style="font-family:Verdana;">: The</span></span><span style="font-family:Verdana;"> </span><span style="font-family:Verdana;">aorto-pulmonary window is a rare congenital heart defect, the diagnosis of which must be made as early as possible in order to avoid the progression to pulmonary hypetension and heart failure.</span>
