The Williams-Beuren syndrome,that we are going to describe, attends with language disorders and hearing problems, reason why we consider interesting study basing on a case rated at Phoniatrics area. This is a prospective study originated since a girl of 18 months arrived to us referred by the Child Neurology Service of Salamanca to her language and development and followed until today. This Syndrome was first described in 1961 by a New Zealand doctor called Dr. Williams, who reported a clinically complex report showing up the most marked symptoms consisted of a characteristic expression of the face, the existence of mental disabilities and a flaw cardiac since birth. Three years later, Professor Beuren, would demostrated that apart from the...
Williams-Beuren syndrome (WBS) is a rare genetic disorder characterized by peculiar facies, eyes, de...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
Williams-Beuren syndrome (WBS) is clinically characterized by a distinctive "elfin" facial appearan...
Williams-Beuren syndrome is a genetic neurodevelopmental disorder that includes different clinical m...
Objetivo: El objetivo es dar a conocer un caso de Síndrome de Williams-Beuren (SWB). Caso Clínico: L...
Williams-Beuren syndrome has an estimated incidence of one case in every 10,000 births. It is second...
Williams-Beuren syndrome (WBS) is a genetic disease caused by a microdeletion in the 7q11.23 region....
Copyright © 2012 Hassan Zamani et al. This is an open access article distributed under the Creative ...
El síndrome de Williams-Beuren , tiene una incidencia de 1 caso por cada 10,000 nacimientos, es caus...
Williams syndrome is known by several names: Beuren\u27s syndrome, Williams-Beuren syndrome, Fanconi...
Whether genetic or environmental influences predominate in defining thought, behavior, and physical ...
Aim:Williams-Beuren syndrome, which is characterized by dysmorphic facial features, cardiovascular f...
El síndrome Williams (SW) es una de las enfermedades raras o infrecuentes. Tiene una incidencia de u...
INTRODUÇÃO: A síndrome de Williams-Beuren (SWB) resulta de uma deleção de aproximadamente 1.5 Mb na ...
Williams-Beuren syndrome is a neurocognitive disorder with multisystemic manifestations of variable ...
Williams-Beuren syndrome (WBS) is a rare genetic disorder characterized by peculiar facies, eyes, de...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
Williams-Beuren syndrome (WBS) is clinically characterized by a distinctive "elfin" facial appearan...
Williams-Beuren syndrome is a genetic neurodevelopmental disorder that includes different clinical m...
Objetivo: El objetivo es dar a conocer un caso de Síndrome de Williams-Beuren (SWB). Caso Clínico: L...
Williams-Beuren syndrome has an estimated incidence of one case in every 10,000 births. It is second...
Williams-Beuren syndrome (WBS) is a genetic disease caused by a microdeletion in the 7q11.23 region....
Copyright © 2012 Hassan Zamani et al. This is an open access article distributed under the Creative ...
El síndrome de Williams-Beuren , tiene una incidencia de 1 caso por cada 10,000 nacimientos, es caus...
Williams syndrome is known by several names: Beuren\u27s syndrome, Williams-Beuren syndrome, Fanconi...
Whether genetic or environmental influences predominate in defining thought, behavior, and physical ...
Aim:Williams-Beuren syndrome, which is characterized by dysmorphic facial features, cardiovascular f...
El síndrome Williams (SW) es una de las enfermedades raras o infrecuentes. Tiene una incidencia de u...
INTRODUÇÃO: A síndrome de Williams-Beuren (SWB) resulta de uma deleção de aproximadamente 1.5 Mb na ...
Williams-Beuren syndrome is a neurocognitive disorder with multisystemic manifestations of variable ...
Williams-Beuren syndrome (WBS) is a rare genetic disorder characterized by peculiar facies, eyes, de...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
Williams-Beuren syndrome (WBS) is clinically characterized by a distinctive "elfin" facial appearan...