Dr. Joshua S. Rotenberg, MD

Dr. Joshua S. Rotenberg, MD http://cdn.hgimg.com/img/prov/Y/5/6/Y566F_w120h160.jpg Get a Free Background Report on Dr. Joshua S. Rotenberg, MD. Malpractice, medical malpractice, sanctions, misconduct, credentials, and penalty or negligence information.

Specializes in Pediatric Neurology • Male • Age 46

902 Frostwood Dr Ste 210
Houston, TX 77024
OverviewPhone & AddressExperienceHospital QualityPatient Satisfaction

Dr. Rotenberg's Experience

Dr. Rotenberg's Care Philosophy

Specialties

  • Pediatric Neurology
  • Adult & Pediatric Neurology
  • Brain Injury Medicine
  • Brain Injury Neurology
  • Epilepsy
  • Epilepsy & Neurophysiology
  • Headache Management
  • Neurodevelopmental Disabilities
  • Neurological Movement Disorders
  • Neurology
  • Pediatric Seizure Disorders
  • Sleep Medicine
  • Sleep Medicine Psychiatry & Neurology
  • Sports Psychiatry & Neurology
  • Teleneurology

Board Certifications

  • Epilepsy
  • Neurology with Special Qualification in Child Neurology
  • Pediatrics
  • Sleep Medicine
1
  • 24-Hour Ambulatory Electroencephalogram
  • ADHD Testing
  • Autonomic Testing
  • Baclofen Pump Therapy
  • Botox® for Chronic Migraine
  • Botox® Injection
  • Chemodenervation
  • Developmental Evaluations
  • EEG (Electroencephalogram)
  • Evaluation and Treatment of Sleep Disorders
  • Infant Care
  • Lumbar Puncture
  • MRI (Magnetic Resonance Imaging)
  • Multiple Sleep Latency Test (MSLT)
  • Neonatal Care
  • Nerve Block, Somatic
  • Neurological Testing
  • Neurostimulation
  • Non-Cosmetic Chemodenervation
  • Polysomnography
  • Premature Infant Care
  • Vagus Nerve Stimulation (VNS)
2
  • 10q Partial Trisomy Syndrome
  • 11q Partial Trisomy Syndrome
  • 14q Partial Trisomy Syndrome
  • 14qter Deletion Syndrome
  • 17,20-Desmolase Deficiency
  • 18-Hydroxylase Deficiency
  • 18p Partial Monosomy Syndrome
  • 1q Terminal Deletion Syndrome
  • Arachnodactyly - Ataxia - Cataract - Aminoaciduria - Mental Retardation
  • Ataxia
  • Ataxia - Apraxia - Mental Retardation, X - Linked
  • Ataxia With Vitamin E Deficiency
  • Ataxia, Hereditary, Autosomal Dominant
  • Ataxia, Spastic, 3, Autosomal Recessive
  • Ataxia-Telangiectasia Syndrome
  • Attention Deficit Disorder (ADD)
  • Attention Deficit Hyperactivity Disorder (ADHD)
  • Attention Deficit Hyperactivity Disorder, Predominantly Inattentive Type
  • Attention Problems
  • Autism
  • Autism, Susceptibility to, 1
  • Autism, Susceptibility to, 10
  • Autism, Susceptibility to, 11
  • Autism, Susceptibility to, 12
  • Autism, Susceptibility to, 13
  • Autism, Susceptibility to, 14
  • Autism, Susceptibility to, 3
  • Autism, Susceptibility to, 4
  • Autism, Susceptibility to, 5
  • Autism, Susceptibility to, 6
More
  • Autism, Susceptibility to, 7
  • Autism, Susceptibility to, 8
  • Autism, Susceptibility to, 9
  • Autism, X-Linked, Susceptibility to, 1
  • Autism, X-Linked, Susceptibility to, 2
  • Autism, X-Linked, Susceptibility to, 3
  • Autonomic Disorders
  • Bell's Palsy
  • Birth Defects
  • Brain Damage
  • Brain Disorders
  • Brain Hemorrhage
  • Brain Injury
  • Brain Lesion
  • CADASIL
  • Carpal Tunnel Syndrome
  • Cerebellar Ataxia
  • Cerebellar Disorders
  • Cerebellar Hypoplasia
  • Cerebral Palsy
  • Cerebral Palsy, Spastic, Diplegic
  • Cerebral Vascular Disease
  • Cerebrovascular Disease
  • Childhood-Onset Cerebral X-Linked Adrenoleukodystrophy
  • Chromosome 1q Deletion Syndrome
  • Chromosome 1q Proximal Deletion Syndrome
  • Concussion
  • Convulsions
  • Cranial Trauma
  • Delayed Sleep Phase Disorder
  • Dementia
  • Developmental Coordination Disorder
  • Developmental Delay
  • Developmental Delay - Epilepsy - Neonatal Diabetes
  • Developmental Delay - Hypotonia Extremities Hypertrophy
  • Developmental Dysphasia, Familial
  • Disruptive Behavior Disorders
  • Down Syndrome
  • Down Syndrome Associated Alzheimer's Disease
  • Down Syndrome Associated Celiac Disease
  • Down Syndrome-Like Hypotonia
  • Dystonia
  • Epilepsy
  • Epilepsy - Mental Deterioration, Finnish Type
  • Epilepsy - Microcephaly - Skeletal Dysplasia
  • Epilepsy - Telangiectasia
  • Epilepsy Occipital Calcifications
  • Epilepsy With Myoclonic Absences
  • Epilepsy With Myoclonic-Astatic Crisis
  • Epilepsy, Benign, Familial, Neonatal
  • Epilepsy, Benign, Neonatal, Dominant Form
  • Epilepsy, Benign, Neonatal, Recessive Form
  • Epilepsy, Benign, Occipital
  • Epilepsy, Familial, Mesial, Temporal Lobe
  • Epilepsy, Familial, Temporal Lobe, 4
  • Epilepsy, Generalized - Paroxysmal Dyskinesia
  • Epilepsy, Idiopathic Generalized
  • Epilepsy, Idiopathic Generalized, Susceptibility to
  • Epilepsy, Idiopathic Generalized, Susceptibility to, 1
  • Epilepsy, Idiopathic Generalized, Susceptibility to, 2
  • Epilepsy, Idiopathic Generalized, Susceptibility to, 3
  • Epilepsy, Idiopathic Generalized, Susceptibility to, 4
  • Epilepsy, Idiopathic Generalized, Susceptibility to, 5
  • Epilepsy, Idiopathic Generalized, Susceptibility to, 6
  • Epilepsy, Myoclonic, Progressive, Familial
  • Epilepsy, Nocturnal, Frontal Lobe Type
  • Epilepsy, Nocturnal, Frontal Lobe Type 1
  • Epilepsy, Nocturnal, Frontal Lobe Type 2
  • Epilepsy, Nocturnal, Frontal Lobe Type 3
  • Epilepsy, Nocturnal, Frontal Lobe Type 4
  • Epilepsy, Partial, Familial
  • Epilepsy, Progressive, Myoclonic 3
  • Epilepsy, Rolandic - Paroxysmal Exercise-Induced Dystonia - Writer's Cramp
  • Epilepsy, X - Linked - Learning Disabilities - Behavior Disorders
  • Epilepsy-Like Myoclonic Jerks
  • Epileptic Encephalopathy, Early Infantile, 1
  • Epileptic Encephalopathy, Early Infantile, 2
  • Epileptic Encephalopathy, Early Infantile, 3
  • Epileptic Encephalopathy, Early Infantile, 4
  • Epileptic Encephalopathy, Lennox-Gastaut Type
  • Essential Tremor
  • Febrile Convulsion
  • Febrile Convulsions, Familial, 1
  • Febrile Convulsions, Familial, 2
  • Febrile Convulsions, Familial, 3
  • Febrile Convulsions, Familial, 4
  • Febrile Convulsions, Familial, 5
  • Febrile Convulsions, Familial, 6
  • Febrile Convulsions, Familial, 7
  • Febrile Convulsions, Familial, 8
  • Febrile Convulsions, Familial, 9
  • Gait Abnormality
  • Genetic Diseases
  • Headache
  • Hydrocephalus
  • Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius
  • Hydrocephalus, Child
  • Infant Epilepsy With Migrant Focal Crisis
  • Infantile Refsum Disease
  • Infantile Sialic Acid Storage Disease
  • Infantile Sleep Apnea
  • Infantile Spasms
  • Infantile Spasms - Broad Thumbs
  • Inflammatory and Toxic Neuropathy
  • Insomnia
  • Intervertebral Disc Herniation
  • Intraventricular Hemorrhage
  • Juvenile Absence Epilepsy
  • Learning Disabilities
  • Lissencephaly, Type 1, Isolated, Without Known Genetic Defects
  • Lyme Disease
  • Mental Retardation - Anophthalmia - Craniosynostosis
  • Mental Retardation - Arachnodactyly - Hypotonia - Telangiectasia
  • Mental Retardation - Athetosis - Microphthalmia
  • Mental Retardation - Behavior Disturbance - Sensorineural Hearing Loss
  • Mental Retardation - Blepharophimosis - Obesity - Web Neck
  • Mental Retardation - Coloboma - Slimness
  • Mental Retardation - Contractural Arachnodactyly
  • Mental Retardation - Dysmorphism - Hypogonadism - Diabetes
  • Mental Retardation - Epilepsy
  • Mental Retardation - Epilepsy - Bulbous Nose
  • Mental Retardation - Epilepsy, X-Linked
  • Mental Retardation - Epileptic Seizures - Hypogonadism - Hypogenitalism - Microcephaly - Obesity
  • Mental Retardation - Gynecomastia - Obesity, X-Linked
  • Mental Retardation - Hip Luxation - G6PD Variant
  • Mental Retardation - Hypocupremia - Hypobetalipoproteinemia
  • Mental Retardation - Hypotonia - Skin Hyperpigmentation
  • Mental Retardation - Hypotonic Facies Syndrome, X-Linked, 1
  • Mental Retardation - Keratoconus - Febrile Seizures - Sinoatrial Block
  • Mental Retardation - Macrocephaly - Coarse Facies - Hypotonia
  • Mental Retardation - Macrocephaly - Short Stature - Craniofacial Dysmorphism
  • Mental Retardation - Microcephaly - Epilepsy - Ataxia Syndrome
  • Mental Retardation - Microcephaly - Phalangeal - Facial Abnormalities
  • Mental Retardation - Microcephaly - Unusual Facies
  • Mental Retardation - Multiple Nevi
  • Mental Retardation - Myopathy - Short Stature - Endocrine Defect
  • Mental Retardation - Nasal Hypoplasia - Obesity - Genital Hypoplasia
  • Mental Retardation - Osteosclerosis
  • Mental Retardation - Polydactyly - Uncombable Hair
  • Mental Retardation - Progressive Spasticity, X - Linked
  • Mental Retardation - Psychosis - Macroorchidism
  • Mental Retardation - Short Broad Thumbs
  • Mental Retardation - Short Stature - Absent Phalanges
  • Mental Retardation - Short Stature - Bombay Phenotype
  • Mental Retardation - Short Stature - Cleft Palate - Unusual Facies
  • Mental Retardation - Short Stature - Deafness - Genital
  • Mental Retardation - Short Stature - Hand Contractures - Genital Anomalies
  • Mental Retardation - Short Stature - Heart and Skeletal Anomalies
  • Mental Retardation - Short Stature - Microcephaly - Eye Anomalies
  • Mental Retardation - Short Stature - Scoliosis
  • Mental Retardation - Short Stature - Unusual Facies
  • Mental Retardation - Skeletal Dysplasia - Abducens Palsy
  • Mental Retardation - Sparse Hair - Brachydactyly
  • Mental Retardation - Spasticity - Ectrodactyly
  • Mental Retardation - Unusual Facies - Talipes - Hand Anomalies
  • Mental Retardation Syndrome, Belgian Type
  • Mental Retardation, Autosomal Recessive, 1
  • Mental Retardation, Autosomal Recessive, 10
  • Mental Retardation, Autosomal Recessive, 11
  • Mental Retardation, Autosomal Recessive, 2
  • Mental Retardation, Autosomal Recessive, 3
  • Mental Retardation, Autosomal Recessive, 4
  • Mental Retardation, Autosomal Recessive, 5
  • Mental Retardation, Autosomal Recessive, 6
  • Mental Retardation, Autosomal Recessive, 7
  • Mental Retardation, Autosomal Recessive, 8
  • Mental Retardation, Autosomal Recessive, 9
  • Mental Retardation, Buenos Aires Type
  • Mental Retardation, Epileptic Seizures - Hypogonadism and Hypogenitalism - Microcephaly - Obesity
  • Mental Retardation, Mietens-Weber Type
  • Mental Retardation, Non-Syndromic, Autosomal Recessive
  • Mental Retardation, Smith-Fineman-Myers Type
  • Mental Retardation, Unexplained
  • Mental Retardation, Wolff Type
  • Mental Retardation, X-Linked
  • Mental Retardation, X-Linked - Acromegaly - Hyperactivity
  • Mental Retardation, X-Linked - Borderline Maoa Metabolism Anomaly
  • Mental Retardation, X-Linked - Brachydactyly - Macroglossia
  • Mental Retardation, X-Linked - Cerebellar Hypoplasia - Distinctive Facial Appearance
  • Mental Retardation, X-Linked - Choreoathesis - Abnormal Behavior
  • Mental Retardation, X-Linked - Corpus Callosum Agenesis - Spastic Quadriparesis
  • Mental Retardation, X-Linked - Craniofacial Dysmorphology - Epilepsy - Ophthalmoplegia - Cerebellar Atrophy
  • Mental Retardation, X-Linked - Cubitus Valgus - Typical Face
  • Mental Retardation, X-Linked - Dystonia - Dysarthria
  • Mental Retardation, X-Linked - Epilepsy - Progressive Joint Contractures - Typical Face
  • Mental Retardation, X-Linked - Gynecomastia - Obesity
  • Mental Retardation, X-Linked - Hypogammaglobulinemia - Progressive Neurological Deterioration
  • Mental Retardation, X-Linked - Hypogonadism - Ichthyosis - Obesity - Short Stature
  • Mental Retardation, X-Linked - Hypotonia - Facial Dysmorphism - Aggressive Behavior
  • Mental Retardation, X-Linked - Hypotonia - Recurrent Infections
  • Mental Retardation, X-Linked - Hypotonic Face
  • Mental Retardation, X-Linked - Macrocephaly - Macroorchidism
  • Mental Retardation, X-Linked - Precocious Puberty - Obesity
  • Mental Retardation, X-Linked Dysmorphism
  • Mental Retardation, X-Linked Recessive - Macrocephaly - Ciliary Dysfunction
  • Mental Retardation, X-Linked Syndromic 7
  • Mental Retardation, X-Linked, 1
  • Mental Retardation, X-Linked, 12
  • Mental Retardation, X-Linked, 14
  • Mental Retardation, X-Linked, 16
  • Mental Retardation, X-Linked, 17
  • Mental Retardation, X-Linked, 2
  • Mental Retardation, X-Linked, 20
  • Mental Retardation, X-Linked, 21
  • Mental Retardation, X-Linked, 23
  • Mental Retardation, X-Linked, 29
  • Mental Retardation, X-Linked, 3
  • Mental Retardation, X-Linked, 30
  • Mental Retardation, X-Linked, 36
  • Mental Retardation, X-Linked, 42
  • Mental Retardation, X-Linked, 43
  • Mental Retardation, X-Linked, 45
  • Mental Retardation, X-Linked, 46
  • Mental Retardation, X-Linked, 49
  • Mental Retardation, X-Linked, 50
  • Mental Retardation, X-Linked, 52
  • Mental Retardation, X-Linked, 53
  • Mental Retardation, X-Linked, 54
  • Mental Retardation, X-Linked, 59
  • Mental Retardation, X-Linked, 63
  • Mental Retardation, X-Linked, 72
  • Mental Retardation, X-Linked, 73
  • Mental Retardation, X-Linked, 77
  • Mental Retardation, X-Linked, 78
  • Mental Retardation, X-Linked, 81
  • Mental Retardation, X-Linked, 82
  • Mental Retardation, X-Linked, 84
  • Mental Retardation, X-Linked, 9
  • Mental Retardation, X-Linked, 91
  • Mental Retardation, X-Linked, 93
  • Mental Retardation, X-Linked, 94
  • Mental Retardation, X-Linked, Armfield Type
  • Mental Retardation, X-Linked, Brooks Type
  • Mental Retardation, X-Linked, Brunner Type
  • Mental Retardation, X-Linked, Cabezas Type
  • Mental Retardation, X-Linked, Cantagrel Type
  • Mental Retardation, X-Linked, Nonspecific
  • Mental Retardation, X-Linked, Pai Type
  • Mental Retardation, X-Linked, Raynaud Type
  • Mental Retardation, X-Linked, Reish Type
  • Mental Retardation, X-Linked, Seemanova Type
  • Mental Retardation, X-Linked, Shrimpton Type
  • Mental Retardation, X-Linked, South African Type
  • Mental Retardation, X-Linked, Stevenson Type
  • Mental Retardation, X-Linked, Stoll Type
  • Mental Retardation, X-Linked, Syndromic 11
  • Mental Retardation, X-Linked, Syndromic 12
  • Mental Retardation, X-Linked, Syndromic 14
  • Mental Retardation, X-Linked, Syndromic, Due to Jarid1c Mutation
  • Mental Retardation, X-Linked, Turner Type
  • Mental Retardation, X-Linked, Vitale Type
  • Mental Retardation, X-Linked, With Isolated Growth Hormone Deficiency
  • Mental Retardation, X-Linked, Wittwer Type
  • Mental Retardation, X-Linked, Zorick Type
  • Migraine
  • Migraine With Aura, Susceptibility to, 9
  • Migraine With or Without Aura, Susceptibility to, 1
  • Migraine With or Without Aura, Susceptibility to, 10
  • Migraine With or Without Aura, Susceptibility to, 11
  • Migraine With or Without Aura, Susceptibility to, 2
  • Migraine With or Without Aura, Susceptibility to, 3
  • Migraine With or Without Aura, Susceptibility to, 4
  • Migraine With or Without Aura, Susceptibility to, 5
  • Migraine With or Without Aura, Susceptibility to, 6
  • Migraine With or Without Aura, Susceptibility to, 7
  • Migraine With or Without Aura, Susceptibility to, 8
  • Migraine, Hormone-Induced
  • Migrainous Stupor Migraine
  • Migrainous Vertigo
  • Mitochondrial Diseases
  • Mitochondrial Diseases, Clinically Indefinite
  • Mitochondrial Encephalomyopathy - Aminoacidopathy
  • Mitochondrial Myopathy - Lactic Acidosis
  • Mitochondrial Neurogastrointestinal Encephalopathy Syndrome
  • Mitochondrial Trifunctional Protein Deficiency
  • Narcolepsy
  • Neonatal Herpes, Type 1 Virus
  • Neonatal Herpes, Type 2 Virus
  • Obesity
  • Pachygyria
  • Pachygyria - Mental Retardation - Seizures
  • Pachygyria, Frontotemporal
  • Pervasive Developmental Disorder (PDD)
  • Petit Mal Seizure
  • Post-Concussion Syndrome
  • Rare Diseases
  • Reflex Sympathetic Dystrophy
  • Restless Leg Syndrome
  • Sedative, Hypnotic, or Anxiolytic Dependence
  • Sleep Apnea
  • Sleep Apnea of Infancy
  • Sleep Deprivation
  • Sleep Disorders
  • Sleep Disturbance-Related Fibromyalgia
  • Sleep Sex
  • Sleep Terror Disorder
  • Sleep-Related Rhythmic Movement Disorder
  • Sleep-Talking
  • Sleep-Walking
  • Spastic Diplegia, Infantile Type
  • Spastic Disorders
  • Spastic Gait
  • Spastic Paraparesis
  • Spastic Quadriplegia - Retinitis Pigmentosa - Mental Retardation
  • Spastic Tetraplegic - Cerebral Palsy
  • Spasticity
  • Spasticity - Mental Retardation
  • Spasticity - Mental Retardation - Epilepsy, X-Linked
  • Spasticity - Multiple Exostoses
  • Speech Delay
  • Speech Impairment
  • Spina Bifida
  • Syncope
  • Tay-Sachs Disease
  • Temporal Epilepsy, Familial
  • Temporal Lobe Epilepsy
  • Temporal Lobe Seizure
  • Tic Disorders
  • Tourette's Syndrome
  • Tremor
  • Vertigo
Less
3

Background Check for Dr. Rotenberg

0 Malpractice Claims

  • No malpractice history found for Texas.
  • No sanctions history found for the years that Healthgrades collects data.

0 Board Actions

  • No board actions found for the years that Healthgrades collects data.
5

Education & Training

Medical School

The Warren Alpert Medical School Of Brown University
Graduated in 1995

Internship Hospital

Lenox Hill/Nyu-Internal Medicine
Complete in 1996

Residency Hospital

Wpafp/Dayton Childrens/Wright State-General Pediatrics
Complete in 2000

Fellowship Hospital

National Capital Consortium-Walter Reed Amc, Nnmc, Nih-Neurology-Child & Adolescent Neurology
Complete in 2003

Undergraduate Schools

Brown Univ
Graduated in 1991

Other Education

Childrens National Medical Center
Kennedy Krieger Inst/Johns Hopkins U
6

Languages Spoken by Dr. Rotenberg & Staff

  • English
Healthgrades

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