Melissa D. Lah, MD
Pediatrics | Medical & Molecular Genetics
Accepting New Patients (Referral Required)
- Biography
- Insurance
- Locations
- Specialties & Details
- Ratings & Reviews
Biography
Dr. Melissa D. Lah specializes in Medical Genetics for Riley Medical & Molecular Genetics. Dr. Lah earned her medical degree at Indiana University School of Medicine. She then completed an internship and residency at Indiana University School of Medicine - Pediatrics and a fellowship at Indiana University School of Medicine - Medical Genetics.
Dr. Lah currently has a rating of 4.8 stars out of 5 with over 50 ratings. Patients say that she is cheerful, respectful, and compassionate.
Dr. Lah's primary location is Riley Medical & Molecular Genetics, 1002 Wishard Blvd, Indianapolis, IN 46202. She also sees patients at an office in Bloomington.
Insurance
Insurance plans accepted by this provider are below.
American Health Plan of Indiana/Majestic Care Management (I-SNP Only)
Cigna
Community Health Alliance
Community Health System
Coventry/First Health
Deaconess OneCare
EyeMed
Lutheran Preferred
MultiPlan/PHCS
NaphCare
Sagamore Health Network
Select Health Network
SIHO
Spectera
Suburban Health Organization
Vision Service Plan (VSP)
Note: Although this listing was accurate at the time of posting, insurances change regularly, and insurance plans listed may not be accepted at all office locations for this provider. Please confirm with your insurance company that this provider is covered by your plan before your appointment.
Locations
Specialties & Details
Specialties:
Pediatrics, Medical & Molecular Genetics
Conditions & Treatments:
Alpha-1 Antitrypsin Deficiency Gene Test, Ashkenazi Jewish Genetic Panel, Cardiovascular Genetics, Cardiovascular Genetics Program, Clinical Genetics, Cystic Fibrosis Program, Cystic Fibrosis Testing, Down Syndrome Screening, Dysmorphology, Genetic Counseling, Genetic Testing, Genetic Testing and Screening, Newborn Screening, Syndromology, Tay-Sachs Test, Teratogen Consultation, ASA, Atrial Septal Defect, Atrioventricular Septal Defect, Autosomal Recessive Disease, Bicuspid Aortic Valve, Birth Defects, Bone Dysplasia, Carnitine Deficiency, Chromosomal Abnormalities, Coarctation of the Aorta, Congenital Heart Defects, Congenital Heart Disease, Connective Tissue Disorders, Cystic Fibrosis, Developmental Delay, Disorders of Sexual Development, Down Syndrome, Fabry, Fatty Acid Oxidation Disorders, Fetal Alcohol Spectrum Disorders, Galactosemia, Gaucher, Genetic Conditions, Genetic Heart Disease, Glutaric Acidemia, Glycogen Storage Diseases, Homocystinuria, Hunter Syndrome, Hurler Syndrome, Hypertrophic Cardiomyopathy, Inborn Metabolism Errors, Inherited Disorders, Klinefelter Syndrome, LCHAD, Maroteaux Lamy Syndrome, MCAD, Metabolism Disorders, Mitochondrial Disorders, MPS, Patent Foramen Ovale, Phenylketonuria, Pompe, PPA, Pulmonary Valve Stenosis, SCAD, Sickle Cell Trait, Sly Syndrome, Tay-Sachs Disease, Tetralogy of Fallot, Thalassemia, Tricuspid Atresia, Turner Syndrome, Tyrosinemia, Urea Cycle Disorders, Vascular Ehlers-Danlos Syndrome, Ventricular Septal Defect, VLCAD, Carbamoyl Phosphate Synthetase Deficiency, Amino Acidopathies, Hyperammonemia, Autism, Intellectual Disability, Cleft Palate, Digeorge Syndrome, Patau Syndrome (Trisomy 13), Edwards Syndrome (Trisomy 18), Congenital Hearing Loss, Beckwith-Wiedemann Syndrome, Russell-Silver Syndrome, Chromosomal Deletions, Chromosomal Duplications, Angelman Syndrome
Education
School of Medicine:
Indiana University School of Medicine
Internship:
Indiana University School of Medicine - Pediatrics
Residency:
Indiana University School of Medicine - Pediatrics
Fellowship:
Indiana University School of Medicine - Medical Genetics
Hospitals & Affiliations
Hospital Privileges:
IU Health Methodist/IU Health University, Riley Hospital for Children at IU Health
Physician Group:
IU Health Medical Group, Riley Physicians
Research
Research Publications
* Information provided by PubMed