Dario Sardella
Biographic Data
| ID | 8258581 |
|---|---|
| NAME | Dario Sardella |
| GIVEN NAMES | Dario |
| FAMILY NAME | Sardella |
| SIGNATURE | SARDELLA D |
| AFFILIATIONS | University of Bari Aldo Moro |
| ORCID | 0009-0004-7347-3199 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2025 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Q11.2 Deletion Syndrome, Oral-Maxillo-Facial Manifestations and Cognitive Functioning
Background: 22q11.2 deletion syndrome (22q11.2 DS) is a rare genetic syndrome characterized by high phenotypic variability, with an incidence of approximately 1:4000 live births. Most of the existing literature consists of case reports or case series, making it challenging to obtain large cohorts for data comparison and drawing generalizable conclusions. Aim: The aim of this article is to share the clinical experience of patients with 22q11.2 DS …
New Trigger for Stroke-like Episode in Sturge–Weber Syndrome
Background . Sturge-Weber syndrome (SWS) is a rare non-hereditary neurovascular disorder characterized by capillary-venous malformations on the face, ocular vascular anomalies, and leptomeningeal capillary-venous malformations. Patients with SWS often experience cerebral perfusion impairment, increasing their risk for stroke-like episodes, seizures, and motor and cognitive impairments. Methods . We report the case of a 2-year-old boy diagnosed wi…
No prominent works on this page.
New Trigger for Stroke-like Episode in Sturge–Weber Syndrome
Background . Sturge-Weber syndrome (SWS) is a rare non-hereditary neurovascular disorder characterized by capillary-venous malformations on the face, ocular vascular anomalies, and leptomeningeal capillary-venous malformations. Patients with SWS often experience cerebral perfusion impairment, increasing their risk for stroke-like episodes, seizures, and motor and cognitive impairments. Methods . We report the case of a 2-year-old boy diagnosed wi…
Q11.2 Deletion Syndrome, Oral-Maxillo-Facial Manifestations and Cognitive Functioning
Background: 22q11.2 deletion syndrome (22q11.2 DS) is a rare genetic syndrome characterized by high phenotypic variability, with an incidence of approximately 1:4000 live births. Most of the existing literature consists of case reports or case series, making it challenging to obtain large cohorts for data comparison and drawing generalizable conclusions. Aim: The aim of this article is to share the clinical experience of patients with 22q11.2 DS …
Anesthesia (1 work) · Bone and Dental Protein Studies (1 work) · Cognition (1 work) · Congenital heart defects research (1 work) · Enamel hypoplasia (1 work) · Hypoplasia (1 work) · Medicine (1 work) · Neuropsychiatry (1 work) · Neurovascular bundle (1 work) · Oral and Craniofacial Lesions (1 work)