Dr. Joshua Rotenberg, MD

Dr. Rotenberg's conditions and procedures:

• 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
• 24-Hour Ambulatory Electroencephalogram
• ADHD and-or ADD
• All Headaches (incl. Migraine)
• Arachnodactyly - Ataxia - Cataract - Aminoaciduria - Mental Retardation
• Ataxia
• Ataxia - Apraxia - Mental Retardation, X - Linked
• Ataxia With Vitamin E Deficiency
• Ataxia-Telangiectasia Syndrome
• Ataxia, Hereditary, Autosomal Dominant
• Ataxia, Spastic, 3, Autosomal Recessive
• Attention Deficit Disorder (ADD)
• Attention Deficit Hyperactivity Disorder, Predominantly Inattentive Type
• Attention Problems
• Autism
• Autoimmune Diseases
• Autonomic Disorders
• Autonomic Testing
• Baclofen Pump Therapy
• Bell's Palsy
• Benign Familial Neonatal Epilepsy
• Birth Defects
• Bone Disorders
• Botox® for Chronic Migraine
• Botox® Injection
• Brain Damage
• Brain Disorders
• Brain Hemorrhage
• Brain Lesion
• CADASIL
• Carpal Tunnel Syndrome
• Cerebellar Ataxia
• Cerebellar Disorders
• Cerebellar Hypoplasia
• Cerebral Palsy
• Cerebral Palsy, Spastic, Diplegic
• Cerebrovascular Disease
• Chemodenervation
• Childhood-Onset Cerebral X-Linked Adrenoleukodystrophy
• Chromosome 1q Deletion Syndrome
• Chromosome 1q Proximal Deletion Syndrome
• Chronic Pain
• Concussion
• Confusion
• Cranial Trauma
• Delayed Sleep Phase Disorder
• 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
• Early Infantile Epileptic Encephalopathy
• EEG (Electroencephalogram)
• 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, 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, 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
• Epileptic Encephalopathy, Lennox-Gastaut Type
• Essential Tremor
• Evaluation and Treatment of Sleep Disorders
• Febrile Convulsion
• Febrile Convulsions, Familial, 1
• Fever-Induced Seizure
• Gait Abnormality
• Genetic Diseases
• Genetic Disposition to Idiopathic Generalized Epilepsy
• Genetic Predisposition to Autism
• Genetic Predisposition to Migraine With or Without Aura
• Headache
• Herniated Disc
• Hydrocephalus
• Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius
• Hydrocephalus, Child
• Infant Care
• 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
• Intraventricular Hemorrhage
• Juvenile Absence Epilepsy
• Learning Disabilities
• Lissencephaly, Type 1, Isolated, Without Known Genetic Defects
• Lumbar Puncture
• 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, 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, Hormone-Induced
• Migrainous Stupor Migraine
• Migrainous Vertigo
• Mitochondrial Diseases
• Mitochondrial Encephalomyopathy - Aminoacidopathy
• Mitochondrial Myopathy - Lactic Acidosis
• Mitochondrial Neurogastrointestinal Encephalopathy Syndrome
• Mitochondrial Trifunctional Protein Deficiency
• MRI (Magnetic Resonance Imaging)
• Multiple Sleep Latency Test (MSLT)
• Myoclonus
• Narcolepsy
• Narcolepsy and Cataplexy
• Neonatal Care
• Neonatal Herpes, Type 1 Virus
• Neonatal Herpes, Type 2 Virus
• Nerve Block, Somatic
• Nerve Root Injury and Plexus Disorders (incl. Pinched Nerve)
• Neurological Testing
• Neurostimulation
• Non-Cosmetic Chemodenervation
• Obesity
• Pachygyria
• Pachygyria - Mental Retardation - Seizures
• Pachygyria, Frontotemporal
• Peripheral Nerve Disorders
• Pervasive Developmental Disorder (PDD)
• Petit Mal Seizure
• Phantom Limb Pain
• Polyneuropathy
• Polyneuropathy Due to Alcohol and Drugs
• Post-Concussion Syndrome
• Premature Infant Care
• Progressive Familial Myoclonic Epilepsy
• Progressive Supranuclear Palsy (PSP)
• Rare Diseases
• Reflex Sympathetic Dystrophy
• Restless Leg Syndrome
• Scoliosis
• Sedative, Hypnotic, or Anxiolytic Dependence
• Seizure Disorders
• Sleep Apnea
• Sleep Deprivation
• Sleep Disorders
• Sleep Disturbance-Related Fibromyalgia
• Sleep Sex
• Sleep Study
• Sleep Terror Disorder
• Sleep-Related Rhythmic Movement Disorder
• Sleep-Talking
• Sleep-Walking
• Spastic Diplegia, Infantile Type
• 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
• Spina Bifida
• Spine Disorders
• Syncope
• Tay-Sachs Disease
• Temporal Epilepsy, Familial
• Temporal Lobe Epilepsy
• Temporal Lobe Seizure
• Tic Disorders
• Tourette's Syndrome
• Traumatic Brain Injury
• Tremor
• Vagus Nerve Stimulation (VNS)
• Vascular Disease
• Vertigo