A5092995670- Vascular Anomalies and Treatments
- Vascular Malformations and Hemangiomas
- Tracheal and airway disorders
- Williams Syndrome Research
- Sharing Economy and Platforms
- Viral Infections and Immunology Research
- Osteomyelitis and Bone Disorders Research
- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Orthopedic Infections and Treatments
- Genetics and Neurodevelopmental Disorders
- Congenital heart defects research
Hospital Italiano de Buenos Aires
2023-2025
Trastuzumab emtansine (T-DM1) is a targeted therapy combining trastuzumab and for human epidermal growth factor receptor 2(HER2)-positive breast cancer, with common side effects including fatigue, nausea, pain, headache, low platelet count, elevated liver enzymes. Hereditary Hemorrhagic Telangiectasia (HHT) an autosomal dominant vascular dysplasia characterized by malformations telangiectasias in various organs. We present case of female patient advanced cancer who developed HHT-like...
Se presenta un niño de 6 años con antecedente retraso del lenguaje que llevó a sus padres realizar múltiples consultas. En primer momento, su cuadro fue interpretado como parte global desarrollo. Posteriormente, el paciente presentó convulsiones y episodios descompensación metabólica, comenzando desde entonces seguimiento por los Servicios neurología, genética metabolismo. Finalmente, tras varios estudios complementarios, medio exoma trío se arribó al diagnóstico síndrome microduplicación...
Here we describe the case of a 2-month-old infant who consulted several times due to excessive crying, initially interpreted as having gastrointestinal cause. Since symptom persisted, fracture was suspected its association with mobilization limbs and palpation mass on anterior aspect right tibia. X-rays showed diaphyseal polyostotic involvement lesions compatible cortical long bones. Caffey-De Toni-Silverman syndrome diagnosed treatment nonsteroidal anti-inflammatory drugs initiated,...