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Changrui Xiao, MD

Medical Genetics
Accepting New Patients
CHOC Children's Specialists - 1201 La Veta Ave.
1201 West La Veta Avenue
Orange, CA 92868
1962.1 miles away
(888) 770-2462
Medical Groups & Affiliations
Providence Affiliated Physicians, St. Joseph
Speaks: English
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CHOC Children's Specialists - 1201 La Veta Ave.

1201 West La Veta Avenue, Orange, CA 92868

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Insurances Accepted

This information provides an overview of accepted insurance plan types. Coverage may vary by specific plan. Please verify your with your insurance provider before visiting us for care.

About Changrui Xiao

Dr. Xiao is board certified who specializes in metabolic disorders and treats kids with genetic diseases at CHOC Hospital in Orange.

Medical School

Duke University
2014

Internship

University of Chicago
Internal Medicine
2015

Residency

University of Chicago
Neurology
2018

Fellowship

National Institute of Health
Medical Genetics
2020

Board Certifications
  • American Board of Medical Genetics and Genomics, Clinical Genetics (MD)
  • American Board of Medical Genetics and Genomics, Medical Biochemical Genetics
  • American Board of Psychiatry and Neurology, Neurology
  • American Board of Medical Genetics and Genomics, Clinical Genetics and Genomics (MD)
CHOC Children's Specialists - 1201 La Veta Ave.
1201 West La Veta Avenue
Orange, CA 92868
Medical Groups & Affiliations
Providence Affiliated Physicians, St. Joseph

Conditions and Procedures

  • Abdominal Wall Defect
  • Abnormal Newborn Screening
  • Achondroplasia
  • Acrocephalosyndactyly
  • Adrenoleukodystrophy (Ald)
  • Aicardi Syndrome
  • Alagille Syndrome
  • Albinism
  • Alpha 1 Antitrypsin Deficiency
  • Alport Syndrome
  • Anal Stenosis
  • Androgen Insensitivity
  • Angelman Syndrome
  • Aniridia
  • Apc Gene
  • Arteriovenous Malformation (Avm)
  • Autism
  • Axin2 Gene
  • Bap1 Gene
  • Bard1 Gene
  • Barth Syndrome
  • Becker Muscular Dystrophy
  • Beckwith Wiedemann Syndrome
  • Bethlem Myopathy
  • Blepharophimosis
  • Blood Disorders
  • Blue Diaper Syndrome
  • Bmpr1a Gene
  • Bohring Opitz Syndrome (Bos)
  • Bone Disorders
  • Brca
  • Breast Cancer Genetic Testing
  • Breast Cancer Genetics
  • Brugada Syndrome
  • C Syndrome
  • Cafe Au Lait Spots
  • Cancer Predisposition Syndromes
  • Cardiac Genetics
  • Cardiomyopathy
  • Carnitine Deficiency
  • Carnitine Disorders
  • Cataract
  • Cdh13 Gene
  • Cdk4 Gene
  • Cdkl5 Mutation
  • Cdkn2a Gene
  • Central Core Disease
  • Cerebellar Anomalies
  • Cerebral Anomalies
  • Cerebral Palsy
  • Charcot Marie Tooth Disease
  • Charge Syndrome
  • Checkpoint Kinase 2
  • Childhood Obesity
  • Chromosomal Microarray Analysis
  • Chromosome Abnormality
  • Chromosome Duplication
  • Chronic Granulomatous Disorder
  • Cirrhosis
  • Cleidocranial Dysostosis
  • Coloboma
  • Congenital Adrenal Hyperplasia
  • Congenital Diaphragmatic Hernia (Cdh)
  • Congenital Esophageal Atresia
  • Congenital Generalized Lipodystrophy
  • Congenital Heart Disease
  • Congenital Hyperinsulinism
  • Congenital Limb Defects
  • Connective Tissue Disorder
  • Cornelia De Lange Syndrome
  • Costello Syndrome
  • Cutis Aplasia
  • Cyp2c19 Mutation
  • Cyp2d6 Mutation
  • Cystic Fibrosis
  • Cystic Fibrosis Gene Carrier
  • Deafness
  • Deficiency Of Interleukin1receptor Antagonist
  • Dejerine Sottas Disease
  • Denys Drash Syndrome (Dds)
  • Developmental Delay
  • Developmental Regression
  • Diabetes Mellitus
  • Diaphragmatic Hernia
  • Dicer1 Gene
  • Digeorge Syndrome
  • Disorders Of Sexual Differentiation
  • Distal Muscular Dystrophy
  • Distal Myopathy
  • Down Syndrome
  • Duane Syndrome
  • Duchenne Muscular Dystrophy
  • Dup15q Syndrome
  • Dystonia
  • Ectodermal Dysplasias
  • Edema
  • Ehlers Danlos
  • Ellis-Van Creveld Syndrome
  • Epcam Gene
  • Epilepsy
  • Esophageal Atresia
  • Exercise Intolerance
  • Facial Asymmetry
  • Facioscapulohumeral Muscular Dystrophy
  • Failure To Thrive
  • Familial Medullary Thyroid Cancer (Fmtc)
  • Familial Partial Lipodystrophy
  • Familial Spinal Muscle Atrophy
  • Family History Of Autism
  • Family History Of Birth Defects
  • Family History Of Cancer
  • Family History Of Colon Cancer
  • Family History Of Colon Polyps
  • Family History Of Glaucoma
  • Fatal Familial Insomnia (Ffi)
  • Fetal Alcohol Syndrome
  • Fetal Growth Restriction
  • Fish Cancer Test
  • Flcn Gene
  • Fracture
  • Fragile X Syndrome
  • Frasier Syndrome
  • Galnt12 Gene
  • Gaucher Disease
  • Genetic Causes Of Vascular Malformations
  • Genetic Counseling
  • Genetic Disorders
  • Genetic Dystonia
  • Genetic Testing Colon Cancer
  • Genetic Testing Ovarian Cancer
  • Glaucoma
  • Glaucoma Of Childhood
  • Glucose Galactose Malabsorption (Ggm)
  • Glycogen Storage Disease
  • Gorlin Syndrome
  • Grem1 Gene
  • Grin Mutation
  • Hearing Loss
  • Hearing Loss (Genetic)
  • Hemihypertrophy
  • Hemochromatosis
  • Hemoglobinopathies
  • Hemophagocytic Lymphohistiocytosis
  • Hemophilia
  • Hemophilia Inhibitors
  • Her2 Positive Breast Cancer
  • Hereditary Hemorrhagic Telangiectasia
  • Hereditary Polyposis
  • Hereditary Retinoblastoma
  • Hereditary Spastic Paraplegia
  • Hermansky Pudlak Syndrome
  • Hirschsprung's Disease
  • Holt-Oram Syndrome
  • Hormone Receptor Positive Breast Cancer
  • Hoxb13 Gene
  • Hunter Syndrome
  • Hurler Syndrome
  • Hydrocephalus
  • Hypermobility Syndrome
  • Hypertrophic Cardiomyopathy
  • Hypoglycemia
  • Hypophosphatasia
  • Hypospadias
  • Hypotonia
  • Immune Deficiency
  • Inborn Errors Of Metabolism
  • Infertility
  • Intellectual Disabilities
  • Intestinal Atresia
  • Ipex Syndrome
  • Kabuki Syndrome
  • Kcnb1 Mutation
  • Kearns Sayre Syndrome
  • Kidney Dysplasia
  • Kit Gene
  • Klinefelter Syndrome
  • Klippel Trenaunay Syndrome
  • Learning Disabilities
  • Learning Disorders
  • Leber Hereditary Optic Neuropathy
  • Leigh's Disease
  • Leukodystrophy
  • Li Fraumeni Syndrome
  • Lissencephaly
  • Long Qt Syndrome
  • Lynch Syndrome
  • Lysosomal Diseases
  • Macrocephaly
  • Marfan Syndrome
  • Maroteaux Lamy Syndrome
  • Maturity Onset Diabetes Of The Young
  • Max Gene
  • Mckusick-Kaufman Syndrome (Mkks)
  • Met Gene
  • Met Proto-Oncogene Receptor Tyrosine Kinase Mutation
  • Metabolic Acidosis
  • Metabolic Disorders (Inherited)
  • Microcephaly
  • Micrognathia
  • Microphthalmos
  • Mitf Gene
  • Mitochondrial Disorders
  • Mlh1 Gene
  • Morquio Brailsford Syndrome
  • Mre11a Gene
  • Msh2 Gene
  • Msh3 Gene
  • Msh6 Gene
  • Mthfr Mutation
  • Mucklewells Syndrome
  • Mucopolysaccharidosis
  • Multifactorial Inheritance
  • Multiple Congenital Anomalies And Birth Defects
  • Multiple Epiphyseal Dysplasia
  • Muscular Dystrophy
  • Mutyh Gene
  • Myoclonic Epilepsy With Ragged Red Fibers
  • Myotonic Dystrophy
  • Nbn Gene
  • Neonatal Adrenoleukodystrophy
  • Neural Tube Defects
  • Neurofibromatosis
  • Neuronal Migration Disorders
  • Neuropathy
  • Neurotransmitter Abnormalities
  • Neutrophil Disorders
  • Niemann Pick Disease
  • Noonan Syndrome
  • Nthl1 Gene
  • Ntric Fusion Mutation
  • Nudt15 Mutation
  • Nystagmus
  • Obesity
  • Opsoclonus Myoclonus Ataxia Syndrome
  • Osteogenesis Imperfecta
  • Osteopetrosis
  • Osteoporosis
  • Paramyotonia Congenita
  • Pdgfra Gene
  • Pediatric Cancer
  • Peroxisomal Disorders
  • Peutz Jeghers Syndrome
  • Phenylketonuria
  • Pierre Robin Sequence
  • Plagiocephaly
  • Pms2 Gene
  • Poland Syndrome
  • Pold1 Gene
  • Pole Gene
  • Polycystic Kidney Disease
  • Polydactyly Hand
  • Porphyria
  • Port Wine Stain
  • Prader Willi Syndrome
  • Precision Medicine
  • Preconception Counseling
  • Prenatal Genetic Counseling
  • Prenatal Testing
  • Preventive Medicine
  • Proto-Oncogene B-Raf And V-Raf Murine Sarcoma Viral Oncogene Homolog B Mutation
  • Ptch1 Gene
  • Rad50 Gene
  • Rad51c Gene
  • Rad51d Gene
  • Rash
  • Rb1 Gene
  • Recurrent Infections
  • Regressive Autism
  • Renal Agenesis And Dysgenesis
  • Retinitis Pigmentosa
  • Rett Syndrome
  • Rnf43 Gene
  • Rps20 Gene
  • San Filippo Syndrome
  • Scn1a Related Seizures Disorders
  • Scn2a Mutation
  • Sdha Gene
  • Sdhaf2 Gene
  • Sdhb Gene
  • Sdhc Gene
  • Sdhd Gene
  • Short Stature
  • Shwachman Diamond Syndrome
  • Slos Smith Lemli Opitz Syndrome
  • Smad4 Gene
  • Smarca4 Gene
  • Smarcb1 Gene
  • Smith-Magenis Syndrome
  • Speech Delay
  • Spinal Muscular Atrophy
  • Splenomegaly
  • Spondylo-Meta-Epiphyseal Dysplasia
  • Stickler Syndrome
  • Sufu Gene
  • Syndactyly
  • Tay Sachs Disease
  • Thumb Hypoplasia
  • Tmem127 Gene
  • Tpmt Mutation
  • Trisomy 13
  • Tuberous Sclerosis
  • Turner Syndrome
  • Twin Types
  • Tyrosinemia
  • Ventriculomegaly
  • Vhl Gene
  • Williams Syndrome
  • Wilms Tumor 1 Mutations
  • Wilson's Disease
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