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Síndrome de Apert, reporte de caso clínico
(Universidad de Cuenca. Facultad de Ciencias Médicas, 2017-04)
Apert syndrome also called acrocephalosyndactyly
Type I is characterized by craniosynostosis , symmetric
syndactyly in all four limbs , mental retardation , skin and
maxillofacial disorders ; It is caused by a mutation ...
Síndrome de Apert, reporte de caso clínicoRevista de la Facultad de Ciencias Médicas. Universidad de Cuenca
(Universidad de Cuenca. Facultad de Ciencias Médicas, 2017)
Beneficio funcional del tratamiento quirúrgico de sindactilia mediante técnica Maccollum y Cronin Hospital Dr. Francisco Icaza Bustamante año 2013-2015
(Universidad de Guayaquil. Facultad de Ciencias Médicas. Escuela de Graduados, 2016)
La Sindactilia es la fusión de dígitos adyacentes. Es una de las más frecuentes malformaciones congénitas de la mano y compromete en mayor porcentaje los dedos medio y anular, afectando sobre todo la parte funcional y ...
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene
(2005)
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252 Trp in the FGFR2 gene: The Apert syndrome is characterized by craniosynostosis and syndactyly of hands and feet. Although most cases are sporadic, ...
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene
(2005)
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252 Trp in the FGFR2 gene: The Apert syndrome is characterized by craniosynostosis and syndactyly of hands and feet. Although most cases are sporadic, ...
Apert syndrome: clinical and radiographic features and case report
(Pontifícia Universidade Católica do Rio Grande do Sul, 2011)
PURPOSE: Apert syndrome is a rare type I acrocephalosyndactyly syndrome characterized by craniosynostosis, severe syndactyly of the hands and feet, and dysmorphic facial features. Presents autosomal dominant inheritance ...
Proceso de atención de enfermería en recién nacido con síndrome de Apert
(Babahoyo: UTB-FCS, 2021, 2021)
Terminal deletion 6P23: a case report
(Wiley-Blackwell, 1990-12-01)
We report on a girl with cleft lip and cleft palate, antimongoloid slant of the palpebral fissures, umbilical hernia, skeletal anomalies, partial syndactyly, hypertonia with increased deep tendon reflexes, psychomotor and ...
Síndrome de Fraser: relato de caso nas vias lacrimais
(Sociedade Brasileira de Oftalmologia, 2014-04-01)
Fraser syndrome is a systemic condition characterized by cryptophthalmos, syndactyly and abnormal genitalia, which may be associated with urinary tract, ear, nose, larynx and skeletal abnormalities. Cryptophthalmos can be ...