Results 221 to 230 of about 108,266 (269)
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Pediatric Annals
It is not unusual to detect congenital anomalies in the neonatal period. Fortunately, many of them are benign and inconsequential. These may include branchial cleft cysts, bifid uvula, oral inclusion cysts, and thyroglossal duct cysts. In the newborn period, it is vital for health care providers to be cognizant of the anomalies.
Stephanie, Reeves, Deepak, Kamat
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It is not unusual to detect congenital anomalies in the neonatal period. Fortunately, many of them are benign and inconsequential. These may include branchial cleft cysts, bifid uvula, oral inclusion cysts, and thyroglossal duct cysts. In the newborn period, it is vital for health care providers to be cognizant of the anomalies.
Stephanie, Reeves, Deepak, Kamat
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Congenital anomalies of the vertebrae
The Indian Journal of Pediatrics, 1958A case having multiple sagittal cleft or “butter-fly” vertebrae and hemivertebrae is presented. The record of such coincidence of two rare anomalies in one case could not be found in the literature. Roentgenological investigations of parents and siblings could possibly throw some more light on the case.
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CONGENITAL ANOMALIES OF THE LUNG
Annals of Internal Medicine, 1960Excerpt Congenital anomalies of the lung in the adult are being recognized with increasing frequency, and an awareness of the possibility of their presence in the differential diagnosis of pulmonar...
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Otolaryngologic Clinics of North America, 2007
Congenital tracheal lesions are rare, but important, causes of morbidity in infants and children. Consequently, experience in their management is limited and dispersed. Given its small diameter, the juvenile trachea is obstructed easily by various natural causes, or following a surgical intervention. The diagnosis of a congenital, tracheal, obstructive
Sandu K, Monnier P
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Congenital tracheal lesions are rare, but important, causes of morbidity in infants and children. Consequently, experience in their management is limited and dispersed. Given its small diameter, the juvenile trachea is obstructed easily by various natural causes, or following a surgical intervention. The diagnosis of a congenital, tracheal, obstructive
Sandu K, Monnier P
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The Journal of Bone and Joint Surgery. British volume, 1979
A review of seventy-one children with sacral anomalies is presented. The aetiology is discussed and a classification of sacral anomalies is suggested, with three groups of patients: agenetic, dysgenetic and dysraphic. The clinical presentation of each group is discussed and the high incidence of congenital visceral and skeletal abnormalities is ...
J K, Stanley, R, Owen, S, Koff
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A review of seventy-one children with sacral anomalies is presented. The aetiology is discussed and a classification of sacral anomalies is suggested, with three groups of patients: agenetic, dysgenetic and dysraphic. The clinical presentation of each group is discussed and the high incidence of congenital visceral and skeletal abnormalities is ...
J K, Stanley, R, Owen, S, Koff
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Congenital Anomalies of the Esophagus
Otolaryngologic Clinics of North America, 2007Normal anatomy, embryology, and congenital anomalies of the esophagus are discussed in this article. The classification, epidemiology, embryology, diagnosis, and management, including outcome following repair of esophageal atresia with or without an associated tracheoesophageal fistula, are described.
Olga, Achildi, Harsh, Grewal
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CONGENITAL ANOMALIES OF THE ESOPHAGUS
Pediatrics, 1950AS THIS is the first general meeting of the Academy since the establishment of a surgical section, it would seem fitting to comment on our hopes for this venture. The last few decades have seen great advances in all fields of medicine. Among the most widely known, perhaps, are insulin, antibiotics, chemotherapy, water balance, vitamin and hormone ...
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Congenital chromosome anomalies
Bulletin der Schweizerischen Akademie der Medizinischen Wissenschaften, 1978The introduction of chromosome banding techniques has led to the detection of a greatly increased number of congenital chromosome anomalies, especially those involving duplication and/or deficiency of short segments of chromosomes. Of most widespread use are the general banding techniques: Q-, G- and R-banding.
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Congenital anomalies of the esophagus
Seminars in Pediatric Surgery, 2010Congenital malformations of the esophagus are frequently encountered by pediatric surgeons, especially esophageal atresia with or without tracheo-esophageal fistula. However, the molecular mechanisms underlying the development of these various anomalies are not clear.
Yousef, El-Gohary +2 more
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Congenital Anomalies of the Stapes
Archives of Otolaryngology - Head and Neck Surgery, 1972A patient with congenital fixation of the stapes by a bony bridge replacing the stapedius tendon is reported. After excision of the bridge the patient's hearing became normal.
L, Podoshin, M, Fradis, D, Zisman
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