Outlook for Neurofi bromatosis Type I Research in the Republic of Bashkortostan
Neurofi bromatosis type I (NF1) is a common hereditary tumour syndrome with autosomal dominant type of inheritance. Average worldwide incidence rate of NF1 is 1:3000, equal in men and women. Th e disease develops with a heterozygous mutation in the oncosupressor neurofi bromin-encoding gene NF1. No...
Saved in:
| Main Authors: | R. N. Mustafin, E. K. Khusnutdinova |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Bashkir State Medical University
2020-07-01
|
| Series: | Креативная хирургия и онкология |
| Subjects: | |
| Online Access: | https://www.surgonco.ru/jour/article/view/488 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Prevalence of Hypopigmented and Cafe-Au-Lait Spots in Idiopathic Epilepsy
by: J Gordon Millichap
Published: (2002-03-01) -
Mapping the Genetic Landscape of Neurofibromatosis: Insights from a Multi-Generational Family Study
by: Praveen Kumar Neela, et al.
Published: (2025-01-01) -
Anaesthetic Considerations in Emergency Lower Segment Caesarean Section in Preeclamptic Parturient with Neurofibromatosis: A Case Report
by: Charmi Hitenbhai Shah, et al.
Published: (2025-06-01) -
Abordagem cirúrgica de neurofibroma gigante Surgical correction of a giant neurofibroma
by: Iana Silva Dias, et al.
Published: (2012-06-01) -
Clinical case of family neurofibromatosis type I
by: O. A. Inozemtsova, et al.
Published: (2025-01-01)