Anca Maria Panaitescu
Biographic Data
| ID | 8261032 |
|---|---|
| NAME | Anca Maria Panaitescu |
| GIVEN NAMES | Anca Maria |
| FAMILY NAME | Panaitescu |
| SIGNATURE | PANAITESCU A M |
| AFFILIATIONS | Carol Davila University of Medicine and Pharmacy |
| ORCID | 0000-0002-9213-6735 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2022 |
| LATEST PUBLICATION YEAR | 2024 |
| H-INDEX | 0 |
Prenatal Features of Mirage Syndrome—Case Report and Review of the Literature
MIRAGE syndrome is a recently described congenital condition characterized genetically by heterozygous gain-of-function missense mutations in the growth repressor sterile alpha domain containing 9 (SAMD9) located on the arm of chromosome 7 (7q21.2). The syndrome is rare and is usually diagnosed in newborns and children with myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, and enteropathy, hence the acronym…
Gestational Alloimune Liver Disease—Case Report
We describe the case of a newborn with the antenatal onset of hepatic failure, which has been investigated for all etiologies that can cause liver damage: infectious, metabolic, genetic, and immune. The lack of a clear answer regarding the etiology and the response to immunoglobulin therapy led us to the diagnosis of gestational alloimmune liver disease. Gestational alloimunne liver disease is an uncommon and very severe cause of neonatal acute l…
No prominent works on this page.
Gestational Alloimune Liver Disease—Case Report
We describe the case of a newborn with the antenatal onset of hepatic failure, which has been investigated for all etiologies that can cause liver damage: infectious, metabolic, genetic, and immune. The lack of a clear answer regarding the etiology and the response to immunoglobulin therapy led us to the diagnosis of gestational alloimmune liver disease. Gestational alloimunne liver disease is an uncommon and very severe cause of neonatal acute l…
Prenatal Features of Mirage Syndrome—Case Report and Review of the Literature
MIRAGE syndrome is a recently described congenital condition characterized genetically by heterozygous gain-of-function missense mutations in the growth repressor sterile alpha domain containing 9 (SAMD9) located on the arm of chromosome 7 (7q21.2). The syndrome is rare and is usually diagnosed in newborns and children with myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, and enteropathy, hence the acronym…
Medicine (2 works) · Pregnancy (2 works) · Amniocentesis (1 work) · Antibody (1 work) · Biology (1 work) · Cirrhosis (1 work) · Congenital gastrointestinal and neural anomalies (1 work) · Disease (1 work) · Electrolyte and hormonal disorders (1 work) · Erythrocyte Function and Pathophysiology (1 work)