Medical Conditions
We have treated patients with the following conditions:
- 4q Deletion Syndrome
- Acquired brain injury
- Achondroplasia
- ADD (Attention Deficit Disorder)
- ADHD (Attention-Deficit/Hyperactivity Disorder)
- Addison’s disease
- Alzheimer’s disease
- Amyotrophic Lateral Sclerosis (ALS)
- Anemia
- Angelman syndrome
- Ankylosing spondylitis
- Anophthalmia
- Anxiety
- Aortic stenosis
- Arrhythmias
- Artificial heart valve
- Artificial joints
- Asperger syndrome
- Asthma
- Atrial fibrillation
- Atrial septal defect
- Autism Spectrum Disorder (ASD)
- Autoimmune diseases
- Bainbridge-Ropers syndrome
- Bardet-Biedl syndrome
- Behçet’s disease
- Benign intracranial hypertension
- Bipolar disorder
- Bleeding disorders
- Blindness
- Cancer
- Cardiomegaly
- Cardiomyopathy
- Cerebellar ataxia
- Cerebral palsy
- Cerebrovascular disease
- CHARGE syndrome
- Charcot-Marie-Tooth disease
- Chiari malformation
- Chromosomal translocation
- Chromosome abnormality
- Chromosome deletion syndrome
- Chronic kidney disease
- Chronic liver disease
- Chronic neuromuscular respiratory failure
- Chronic obstructive pulmonary disease (COPD)
- Chronic pain syndrome
- Cleft lip
- Cleft palate
- Congenital heart disease
- Congenital malrotation of the intestine
- Congestive heart failure
- Cornelia de Lange syndrome
- Coronary artery disease
- Cri du Chat syndrome
- Crohn’s disease
- Cyclic vomiting syndrome
- Cystic fibrosis
- Dandy-Walker malformation
- Deafness
- Deep vein thrombosis (DVT)
- Dementia
- Desbuquois syndrome
- Developmental delay
- Diabetes
- DiGeorge syndrome
- Down syndrome
- DSG2 gene mutation
- Duchenne muscular dystrophy
- Dysphagia
- Ectodermal dysplasia
- Edwards syndrome (Trisomy 18)
- Ehlers-Danlos syndrome
- Empty sella syndrome
- Encephalopathy
- End-stage renal disease (ESRD)
- Epilepsy
- Factor VII deficiency
- Factor IX deficiency
- Factor X deficiency
- Fetal alcohol syndrome
- Fetal hydantoin syndrome
- FG syndrome
- Fibrodysplasia ossificans progressiva (FOP)
- Fibromyalgia
- Fragile X syndrome
- Gastroesophageal reflux disease (GERD)
- Gastrostomy tube (G-tube)
- Glucose transporter type 1 deficiency syndrome (GLUT1 deficiency)
- Goldenhar syndrome
- Heart murmur
- Hemophilia
- Hepatitis B
- Hepatitis C
- High BMI
- Hirschsprung disease
- HIV/AIDS
- Holoprosencephaly
- Hunter syndrome (MPS II)
- Hurler syndrome (MPS I)
- Hydrocephalus
- Hypercalcemia
- Hypernatremia
- Hypertension
- Hyperthyroidism
- Hypotension (Low blood pressure)
- Hypothyroidism
- Hypotonia
- ICD (Impulse Control Disorder)
- IED (Intermittent Explosive Disorder)
- Incontinence (fecal and urinary)
- Intellectual disability
- Juvenile idiopathic arthritis
- Kabuki syndrome
- Kanner syndrome
- Klinefelter syndrome
- Lennox-Gastaut syndrome
- Lesch-Nyhan syndrome
- Leukemia
- Lissencephaly
- Lung fibrosis
- Lupus (Systemic Lupus Erythematosus)
- Marfan syndrome
- Metabolic syndrome
- Microcephaly
- Mitochondrial Complex III deficiency
- Mitochondrial encephalopathy
- Moebius syndrome
- Movement disorders
- Muscular dystrophy
- Myasthenia gravis
- Neurofibromatosis
- Noonan syndrome
- Non-verbal
- Obesity
- Obsessive-Compulsive Disorder (OCD)
- Ogilvie syndrome
- Oppositional Defiant Disorder (ODD)
- Oral myiasis
- Osteogenesis imperfecta
- Osteoporosis
- Pacemaker
- Panic disorder
- Paralysis
- Parkinson’s disease
- PDD (Pervasive Developmental Disorder)
- PEG tube
- Peripheral neuropathy
- Pediatric acute-onset neuropsychiatric syndrome (PANS)
- Pediatric autoimmune neuropsychiatric disorder associated with Strep (PANDAS)
- Pierre Robin sequence
- Pica
- Polycystic Ovary Syndrome (PCOS)
- Post-Traumatic Stress Disorder (PTSD)
- Prader-Willi syndrome
- Premenstrual Dysphoric Disorder (PMDD)
- Psychosis
- Pulmonary hypertension
- Pulmonic stenosis
- Rare genetic disorders
- Raynaud’s disease
- Restless legs syndrome
- Rett syndrome
- Ring Chromosome 20 syndrome
- Rubinstein-Taybi syndrome
- Sarcoidosis
- Schizoaffective disorder
- Schizophrenia
- Scleroderma
- Scoliosis
- Seizure disorders
- Self-injurious behavior
- Sickle cell anemia
- Sickle cell disease
- Sickle cell trait
- Sjögren’s syndrome
- Sleep apnea
- Sleep disorders
- Smith-Magenis syndrome
- Spastic quadriplegia
- Spina bifida
- Spinal fusion
- Spinal muscular atrophy (SMA)
- Status epilepticus
- Stroke (CVA)
- Sturge-Weber syndrome
- T12 spinal disorder
- Temporomandibular Joint Disorder (TMJ/TMD)
- Tetralogy of Fallot
- Thalassemia
- Thrombocytopenia
- Thrombocytosis
- Tourette syndrome
- Traumatic brain injury (TBI)
- Transposition of the great arteries
- Transthyretin Amyloid Cardiomyopathy (ATTR-CM)
- Treacher Collins syndrome
- Trisomy 13 (Patau syndrome)
- Tuberous sclerosis
- Turner syndrome
- Ulcerative colitis
- VACTERL association
- Vagus nerve stimulator (VNS)
- Ventricular septal defect (VSD)
- Ventriculoperitoneal (VP) shunt
- Von Willebrand disease
- Waardenburg syndrome
- Wheelchair, walker, or stretcher assistance
- Williams syndrome
- Wilson’s disease
- Wolf-Hirschhorn syndrome
- Wolff-Parkinson-White syndrome
- Xia-Gibbs syndrome
- Zellweger syndrome
