Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Juan Arbués Gabarre"'
Autor:
David, Escribano Abad, Juan, Arbués Gabarre, Enery, Gómez Montes, José Manuel, Puente Agueda, Ignacio, Herraiz García, Alberto, Galindo Izquierdo
Publikováno v:
Ginecologia y obstetricia de Mexico. 79(8)
Otocephaly is a rare and lethal congenital malformation characterized by the presence of agnathia, microstomia, aglossia and synotia. Despite its frequent association with severe malformations, diagnosis in the few published cases is usually made at
Autor:
Ana Moreno Izquierdo, David Escribano Abad, Carmen Lopez-Sanchez, Alberto Galindo Izquierdo, Juan Arbués Gabarre, Virginio Garcia-Martinez
Publikováno v:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine. 25(11)
allister-Killian syndrome (PKS, also referred as tetrasomy 12p) is a rare sporadic chromosomic anomaly characterized by the presence, most often in a mosaic arrangement, of isochromosome 12p.1–3 Patients have 4 copies of the short arm of chromosome
Autor:
Pedro de la Fuente Pérez, Miguel Rasero Ponferrada, José Manuel Puente Agueda, Carlos Orbea Gallardo, Alberto Galindo Izquierdo, Juan Arbués Gabarre
Publikováno v:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine. 24(6)
Pulmonary agenesis refers to the total absence of pulmonary parenchyma and blood vessels as well as bronchia beyond the bifurcation. It is classified as bilateral complete agenesis, unilateral agenesis, and lobar agenesis. The anomaly was first descr