Shubhangi Peche, MD

Description

I strive to provide highest quality of care delivered in a personal respectful and caring environment. Me and my entire office committed to treating each patient with respect and compassion.

Keywords brain injury rehabilitation, cerebral heterotopia, encephalopathies, costello syndrome, cloves syndrome, development coordination disorder, developmental disabilities, cerebral dysgenesis, congenital anomalies of the central nervous system, hemifacial microsomia, juvenile spinal muscular atrophy, myelitis, congenital brain malformations, congenital ataxia, mitochondrial disorders, epilepsy, juvenile myoclonic epilepsy, erb palsy, diffuse cerebral sclerosis, moebius syndrome, muscle weakness, muscle eye brain disease, concussive seizure, cornelia de lange syndrome, muscular dystrophy, myasthenia gravis, brain injury, landau kleffner syndrome, facioscapulohumeral muscular dystrophy, guillain barre syndrome (gbs), learning disorders, hereditary sensory and autonomic neuropathy, metabolic myopathy, muscular disorder, autonomic dysreflexia, hemidystonia, hemicrania continua, multiple sclerosis, hemiparesis, hemineglect, infantile hemiplegia, hemiplegia, benign paroxysmal torticollis of infancy, genetic dystonia, generalized seizures, concussion, microcephaly, dopamine responsive dystonia, arnold chiari malformation type 1, arnold chiari malformation type 2, niemann pick disease, torticollis, cerebral palsy, congenital deformity of nervous system, polymicrogyria, ataxia, torsion dystonia, pseudotumor cerebri, problems with smell and taste, cns vasculitis, tay sachs disease, speech disorder, hypertonia, abnormal eeg, brachycephaly, dup15q syndrome, aicardi syndrome, congenital cerebral hemiatrophy, agenesis of brain, congenital cerebral hypoplasia, quadriplegia, periventricular leukomalacia, cephalocele, neurologic complications of meningitis, pediatric epilepsy, distal myopathy, chronic infantile neurologic cutaneous and articular syndrome, congenital hydrocephalus, sturge weber syndrome, carbidopa levodopa oral therapy, pachygyria, cerebral anomalies, transient limb paralysis, emery dreifuss muscular dystrophy, cranial nerve injury, cerebral degeneration in childhood, post traumatic amnesia, small fiber neuropathy, spina bifida, vein of galen malformation, paroxysmal hemicrania, vagus nerve disease, duchenne muscular dystrophy, rett syndrome, lissencephaly, neurocutaneous syndromes, peripheral nerve injury, febrile convulsions, vertigo, tibial neuropathy.