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Hace 5 días · Moebius syndrome is a rare congenital disorder characterized by congenital bilateral absence of the VI and VII cranial nerves, resulting in facial and horizontal gaze paralysis. In addition to the neurological manifestations, patients with Moebius syndrome may present a variety of ocular abnormalities, including strabismus, nystagmus, and eyelid abnormalities.
Hace 5 días · El Síndrome de Moebius es una enfermedad genética rara y poco conocida que se caracteriza por la parálisis facial y la incapacidad para mover los ojos lateralmente. Esta condición puede tener un impacto significativo en la vida de quienes la padecen, así como en sus familias y cuidadores.
Hace 4 días · Moebius syndrome consists of bilateral palsies of cranial nerves VI and VII, but occasionally also cranial nerves V, X, XI, and XII, resulting in difficulties with chewing, swallowing, and coughing, often leading to aspiration with respiratory complications.
Hace 4 días · This procedure can either be performed in a single stage or 2 stages, depending on the underlying etiology of the facial nerve paralysis. In cases of bilateral facial nerve paralysis (most commonly Moebius syndrome), the free muscle transfer is performed in one stage and the donor innervation is most commonly the ipsilateral masseteric nerve.
Hace 5 días · In Möbius syndrome (congenital facial diplegia), a sixth nerve palsy causing esotropia is associated with palsies of the 7th and 12th cranial nerves and limb deformities Duane syndrome can affect the medial or lateral rectus muscles (or both); may be an isolated defect or may be associated with a multitude of systemic defects (eg ...
Hace 5 días · Moebius Syndrome: Congenital facial diplegia as a result of underdevelopment of the sixth and seventh cranial nerves. Impaired ability to suck in the infancy period often leads to the diagnosis. Excessive drooling and crossed eyes may be present.
Hace 5 días · Dysgenesis of the corpus callosum may be complete (agenesis) or partial (dysgenesis) and represents an in utero developmental anomaly. It can be divided into: primary agenesis: corpus callosum never forms. secondary dysgenesis: corpus callosum forms normally and is subsequently destroyed.
