CONTENT AND DISTRIBUTION OF HAPTOGLOBIN PHENOTYPES IN CHILDREN WITH CEREBRAL PALSY COMPLICATED BY SYMPTOMATIC EPILEPSY

Authors

Artykova Mavlyuda Abdurakhmanovna Doctor of Medical Sciences Head of the Department of Pediatric Neurology and Medical Genetics, Bukhara State Medical Institute named after Abu Ali ibn Sina
Nabiyeva Nozima Abdurakhimovna Assistant of the Department of Pediatric Neurology and Medical Genetics, Bukhara State Medical Institute named after Abu Ali ibn Sina

Keywords:

Cerebral palsy, childhood disability, pathological process, haptoglobin

Abstract

The genetic aspects of the development of various diseases are attracting close attention of researchers. Discussions are underway about the genetic predisposition of an individual to a particular pathology. First of all, this is relevant in the development of hereditary neurological diseases, many of which are manifested in early childhood