Maria S Chico, ACPNP

Description

I enjoy working with children and helping their parents understand the complexities of neurologic chronic illnesses and am committed to providing compassionate care in a supportive environment.

Keywords brain injury rehabilitation, infantile hemiplegia, hemiplegia, hemiparesis, hemineglect, hemifacial microsomia, hemidystonia, hemicrania continua, head trauma, guillain barre syndrome (gbs), glycogen storage disease, genetic dystonia, generalized seizures, friedreich ataxia, focal seizures, focal dystonia, flaccid hemiplegia, fasciculations, familial spinal muscle atrophy, familial ataxia, facioscapulohumeral muscular dystrophy, facial paresis, facial nerve palsy, fabry disease, erb palsy, encephalopathies, encephalitis, emery dreifuss muscular dystrophy, dystonia, dyslexia, dysautonomia, dysarthria, duchenne muscular dystrophy, down syndrome, dopamine responsive dystonia, diffuse cerebral sclerosis, developmental disabilities, demyelinating disease, cranial nerve injury, cornelia de lange syndrome, congenital paralysis, congenital myopathies, congenital myasthenic syndromes, congenital muscular dystrophy, congenital macrocephaly, congenital lesions of the nervous system, congenital hydrocephalus, congenital deformity of nervous system, congenital cerebral hypoplasia, congenital cerebral hemorrhage, congenital cerebral hemiatrophy, congenital brain malformations, congenital ataxia, congenital anomalies of the central nervous system, concussive seizure, chronic infantile neurologic cutaneous and articular syndrome, childhood epilepsy, charcot marie tooth disease, cerebrovascular accident (cva), cerebral palsy, cerebral heterotopia, cerebral dysgenesis, cerebral degeneration in childhood, cerebral anomalies, primary cerebellar degeneration, cerebellar disease, spinocerebellar ataxia, cephalocele, brachycephaly, behcet syndrome, becker muscular dystrophy, autonomic nervous system disorders, autonomic dysreflexia, autism, auditory processing disorder (apd), ataxia, asymmetrical crying facies, arnold chiari malformation type 4, arnold chiari malformation type 3, arnold chiari malformation type 2, arnold chiari malformation type 1, anencephaly, agenesis of brain, agenesis of the corpus callosum, abdominal migraine, tremor, concussion, carbidopa levodopa oral therapy, increased intracranial pressure, merosin deficient congenital muscular dystrophy, fukuyama congenital muscular dystrophy, benign focal amyotrophy, distal myopathy, paramyotonia congenita, distal muscular dystrophy, dejerine sottas disease, central core disease, bethlem myopathy, agnosia, small fiber neuropathy.