22q11.2 DELETION SYNDROME: ALGORITHM FOR THE EARLY DIAGNOSIS AND TREATMENT
Chromosomal diseases, in particular microdeletions, determine the child's condition as well as the prognosis for a disease even at birth. With timely identified chromosomal abnormalities, we can diagnose not only obvious but also hidden disorders in the organs and their systems and timely corre...
Saved in:
Main Authors: | Leyla S. Namazova-Baranova, Olga V. Ginter, Tatyana A. Polunina, Irina V. Davydova, Kirill V. Savostyanov, Alexandr A. Pushkov, Natalya V. Jourkova, Tatyana Y. Mospan |
---|---|
Format: | Article |
Language: | English |
Published: |
"Paediatrician" Publishers LLC
2017-11-01
|
Series: | Вопросы современной педиатрии |
Subjects: | |
Online Access: | https://vsp.spr-journal.ru/jour/article/view/1807 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
22q11.2 Deletion Syndrome: Symptoms, Diagnosis, Treatment
by: Leyla S. Namazova-Baranova, et al.
Published: (2016-12-01) -
FAMILIAL CASE OF CHROMOSOME 22q11.2 DELETION SYNDROME
by: I. A. Tuzankina, et al.
Published: (2017-01-01) -
Variability of CATCH-22 symptome complex within the framework of 22q11.2 deletion syndrome
by: D. A. Cheremokhin, et al.
Published: (2021-12-01) -
Understanding obesity in children with 22q11.2 deletion syndrome
by: Walter Maria Sarli, et al.
Published: (2025-07-01) -
Investigating the relationship between sleep disturbances and psychopathology In children and adolescents with microdeletion of 22q11 chromosome: an exploratory study
by: Maria Rosaria Lala, et al.
Published: (2025-07-01)