Ewelina Perdas
Dados Biográficos
| ID | 8261498 |
|---|---|
| NOME | Ewelina Perdas |
| PRENOMES | Ewelina |
| SOBRENOME | Perdas |
| ASSINATURA | PERDAS E |
| AFILIAÇÕES | Medical University of Lodz |
| ORCID | 0000-0002-2321-2976 |
| VERIFICADO | Sim |
| TOTAL DE OBRAS | 1 |
| TOTAL DE CITAÇÕES | 0 |
| OBRAS COMO AUTOR | 1 |
| OBRAS COMO EDITOR | 0 |
| PRIMEIRO ANO DE PUBLICAÇÃO | 2025 |
| ANO MAIS RECENTE DE PUBLICAÇÃO | 2025 |
| ÍNDICE H | 0 |
Analysis of the Occurrence of PIK3CA Gene Mutation in Children with Lymphatic Malformation—Single Center Study
Background : Lymphatic malformations (LM) are rare congenital vascular anomalies caused by abnormal development and growth of lymphatic vessels. These malformations can lead to a wide range of symptoms, from mild swelling to more severe complications. Treatment options remain limited, especially for complex cases. Recent research has suggested that PIK3CA mutations play a key role in the pathogenesis of LM, potentially offering new possibilities …
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Analysis of the Occurrence of PIK3CA Gene Mutation in Children with Lymphatic Malformation—Single Center Study
Background : Lymphatic malformations (LM) are rare congenital vascular anomalies caused by abnormal development and growth of lymphatic vessels. These malformations can lead to a wide range of symptoms, from mild swelling to more severe complications. Treatment options remain limited, especially for complex cases. Recent research has suggested that PIK3CA mutations play a key role in the pathogenesis of LM, potentially offering new possibilities …
Digital polymerase chain reaction (1 obra) · Gene (1 obra) · Germline mutation (1 obra) · Lymphatic Disorders and Treatments (1 obra) · Lymphatic system (1 obra) · Mutation (1 obra) · Mutation testing (1 obra) · Pathogenesis (1 obra) · Proteus syndrome (1 obra) · Vascular Anomalies and Treatments (1 obra)