Pediatric Endocrinology and Medical Genetics

The Department of Pediatric Endocrinology and Medical Genetics is the first and only department where children with endocrine and hereditary diseases receive individualized treatment.
A qualified team of department specialists utilizes a comprehensive approach to diagnosing and treating conditions such as diabetes mellitus, diabetes insipidus, osteoporosis, hypoglycemia, developmental disorders, disorders of sexual development, the thyroid, parathyroid, pituitary glands dysfunction, adrenal disease, and other endocrinological disorders.

Geneticists provide counseling and examination for families with suspected or probable hereditary diseases to diagnose or prevent genetic diseases early. They also provide required medical care for patients with diagnosed conditions, such as chromosomal abnormalities, congenital and hereditary syndromes or diseases, multiple complex malformations. Availability of all the required investigations at the NCMC Laboratory allows providing all these services with high-quality, in compliance with international standards, and on time.