NOONAN SYNDROME WITH MULTIPLE LENTIGINES CAUSED BY COMMON VARIANT IN THE PTPN11 GENE
The article presents an analysis of literature data concerning the clinical manifestations and molecular diagnosis of Noonan syndrome with multiple lentigines, as well as clinical case of this syndrome.
Authors
- А.А. Гусина (ORCID: https://orcid.org/0000-0003-2670-5634)
- O.L. ZOBIKOVA
- A.S. STALYBKA
- I.V. KOLODKO
- J.Z. NICOLAYEVA
Publication Details
- Journal
- MODERN PERINATAL MEDICAL TECHNOLOGIES IN SOLVING THE PROBLEM OF DEMOGRAPHIC SECURITY
- Published
- 2024-12-01
- DOI
- https://doi.org/10.63030/2307-4795/2024.17.g.14
- Primary Topic
- Protein Tyrosine Phosphatases
- Type
- article
- Field-Weighted Citation Impact
- 0.00