نتایج جستجو برای: encephalocele
تعداد نتایج: 675 فیلتر نتایج به سال:
BACKGROUND In the past, northern China's Shanxi Province has reported the highest incidence of neural tube defects (NTDs) in the world. However, little is known about the epidemiology of NTDs in this area in recent years. METHODS Data were collected from a population-based birth defects surveillance system in 4 counties that captures information on all live births, stillbirths of at least 20 ...
Meckel-Gruber syndrome is a rare autosomal recessive lethal malformation characterized by typical manifestations of occipital encephalocele, bilateral polycystic kidneys and post axial polydactyly. The worldwide incidence varies from 1 in 13,250 to 1 in 140,000 live births. Highest incidence was reported in Gujarati Indians. We report a rare case of Meckel-Gruber syndrome and review of literature.
Meckel-Gruber syndrome (MGS) is an autosomal recessive disorder characterized by occipital encephalocele, polycystic kidneys and variable other congenital malformations. We report on a Sudanese patient with MGS diagnosed by antenatal ultrasound scan. Pregnancy was terminated at 25 weeks of gestation.
Increasing experience and the introduction of new techniques in the treatment of congenital hydrocephalus demand its earliest possible recognition and knowledge of its natural history. By far the commonest type of congenital hydrocephalus is the one associated with a meningomyelocele or encephalocele. The presence of hydrocephalus in such infants should be suspected at birth, simply because the...
DESCRIPTION A 2-year-old boy presented with an atypical craniofacial cleft going through the right nostril with a soft-tissue extension of 2 × 1 cm. A computed tomographic scan showed bony involvement of the right nasal bone, right frontal bone, anterior cribriform plate anomalies, and no encephalocele.
Nasopharyngeal teratoma, commonly known as an epignathus, is a rare congenital malformation found in newborns. Diagnosis is usually straightforward , with calcifications seen within the mass. However, we encountered a neonate with a noncalcified cystic mass protruding from the oral cavity . The question was raised clinically as to whether this could be a basal encephalocele. CT led to the corre...
BACKGROUND Knobloch syndrome is a rare, autosomal recessive, developmental disorder characterized by stereotyped ocular abnormalities with or without occipital skull deformities (encephalocele, bone defects, and cutis aplasia). Although there is clear heterogeneity in clinical presentation, central nervous system malformations, aside from the characteristic encephalocele, have not typically bee...
1. Pierre-Filho Pde T, Limeira-Soares PH, Marcondes AM. Morning glory syndrome associated with posterior pituitary ectopia and hypopituitarism. Acta Ophthalmol Scand. 2004;82:89--92. 2. López-Lizárraga EP, Bolaños-Jiménez R, Treviño-Alanís MG, Rivera-Silva G. Morning glory syndrome. Gac Med Mex. 2011;147:70--1. 3. Tanimoto K, Onda S, Sawaki H, Hiraiwa T, Sano H, Ohnishi M, et al. Hypopituitaris...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید