نتایج جستجو برای: congenital
تعداد نتایج: 120294 فیلتر نتایج به سال:
congenital myopathies are a clinically and genetically heterogeneous group of inherited muscle disorders characterized clinically by reduced fetal movements, hypotonia, weakness and developmental delay beginning at birth or in the first year of life. however, there can be a wide variation in clinical findings including mild and asymptomatic presentation to a severe form within each subtype with...
Over the past four years (1360-1364) we have surgically treated seven infants for lobar emphysema. The pathologic lesion in all patients was in upper lobe of the left lung. Respiratory distress and pneumonia are the cardinal symptoms of patients with this abnormality. Diagnosis is confirmed by chest x-ray. The treatment of choice is lobectomy of affected lobe.
the congenital gingival granular cell tumor (cgct), also as known as congenital epulis, is an unusual benign oral mucosal lesion in newborns. a two-day-old female patient was admitted to the department of pediatric dentistry at gulhane medical academy, ankara, turkey with her family, and an intraoral examination showed a cgct located in the buccal region of the maxillary right first primary mol...
OBJECTIVE To analyze the trend and spatial distribution of infant mortality from congenital malformations in Argentina between 2002 and 2006. MATERIALS AND METHODS Data were provided by the Ministry of Public Health. Congenital malformations were classified according to the International Classification of Diseases, 10th revision. Early neonatal, late neonatal and postneonatal infant mortality...
Background: Neonatal deaths stand for almost two-thirds of all deaths occurring in infants under one year of age. Congenital anomalies are responsible for 24.5% of these cases forming a highly important issue for health policy-makers.Methods: We studied the pre-, peri- and post-natal conditions of 77 patients with multiple congenital anomalies (MCA) through genetic counseling at Several univers...
Congenital dislocation of the knee (CDK) is a rare congenital anomaly and the incidence of the CDK is estimated as 1 per 100,000 births. Diagnosis is made through clinical inspection and X-ray radiography. Our patient is a newborn male with congenital dislocation of the left knee. After diagnosis, the knee was reduced successfully within 24 hours of birth and then serial casting was performed. ...
Congenital Myasthenic Syndromes (CMS) are rare inherited disorders characterized by dysfunction of neuromuscular transmission at the neuromuscular junction. Most patients with congenital myasthenic syndromes present in the infancy. Major symptoms of affected individuals include weakness and fatigue during the first years of life. Patients may show hypotonia, facial weakness, swallowing difficul...
conclusions this case indicates that delineation of coronary artery anatomy in atypical congenital giant right atrial aneurysm is of vital importance. closure of the aneurysmal sac, instead of aneurysmal resection, is a safer and more simple approach in atypical cases. case presentation this is a report on a 3.5-month-old male infant with imperforated anus and an unusual-shaped congenital giant...
We are reporting an infant with persistent abnormal liver function, neonatal jaundice, and intermittent hypoglycemia. Evaluation confirmed congenital hypopituitarism, in the absence of congenital anomalies and midline defect. His jaundice and abnormal liver function improved after treatment with Levothyroxine and hydrocortisone.
Congenital hepatic fibrosis (CHF) is a rare disease that primarily involves hepatobiliary and renal systems. It is characterized by hepatic fibrosis, portal hypertension and renal cystic disease. We present a 22 years old man with fever, abdominal pain, icterus and hematemesis. On complete work up of the patient and liver with kidney biopsy, the diagnosis was congenital hepatic fibrosis.
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