Dr. Shruti Bajaj offers specialized genetic consultation and evaluation across a broad spectrum of medical disciplines.
Mental retardation, autism, ADHD, learning disability, head size abnormalities, epilepsy, balance disorders, psychiatric conditions.
Inborn errors of metabolism, lysosomal storage disorders, porphyria, fatty acid oxidation disorders, aminoacidopathies, organic acidemias.
Short stature, failure to thrive, childhood onset diabetes, recurrent pancreatitis, hyperlipidemia, congenital adrenal hyperplasia.
Congenital heart disease, cardiomyopathy, cardiac conduction defects and hereditary cardiac syndromes.
Early onset nephrotic syndrome, renal malformations, polycystic kidney, haemolytic uremic syndrome, genetic renal tubulopathies.
Unexplained and recurrent pregnancy losses, infertility, premature ovarian failure, consanguineous couple genetic counseling.
Hereditary eye diseases, retinal dystrophies, congenital eye abnormalities, optic neuropathies.
Disproportionate short stature, recurrent fractures, suspected Marfan syndrome, familial joint dislocations.
Neonatal cholestasis, Wilson disease, inherited liver diseases.
Ichthyosis, epidermolysis bullosa, neurofibromatosis, incontinentia pigmenti.
Thalassemia, hemophilia, hereditary spherocytosis, inherited bone marrow failure syndromes, familial cancers.
Cystic fibrosis, primary ciliary dyskinesia, alpha-1 antitrypsin deficiency.
Cleft lip/palate, clubfoot, neural tube defects, congenital diaphragmatic hernia.
Facial asymmetry, abnormal facial features.
Severe combined immunodeficiency, chronic granulomatous disease, Wiskott-Aldrich syndrome.
Down syndrome, Turner syndrome, Klinefelter syndrome, microdeletion syndromes.
Of a known or suspected genetic disorder.