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Valeria Capra

Biographic Data

ID7875927
NAMEValeria Capra
GIVEN NAMESValeria
FAMILY NAMECapra
SIGNATURECAPRA V
AFFILIATIONSIstituto Giannina Gaslini
ORCID0000-0002-3097-0388
VERIFIEDYes
TOTAL WORKS1
TOTAL CITATIONS0
WORKS AS AUTHOR1
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2021
LATEST PUBLICATION YEAR2021
H-INDEX0
  • Oro-Dental Manifestations in a Pediatric Patient Affected by Helsmoortel-Van der Aa Syndrome

    Open Access•Massimo Petruzzi, Alessandro Stella et al.•ARTICLE•International Journal of…•2021

    Aim : Aim of this case report is to describe oro-facial abnormalities in a patient affected by Helsmoortel-Van der Aa syndrome, a rare autism syndrome, with not well described dental and cranial malformations. Case Report : Helsmoortel-Van der Aa Syndrome is a rare autosomal genetic syndrome causing mental impairment and autism, craniofacial dysmorphism, chest deformity and multiple organs dysfunction. Oro-facial involvement in Helsmoortel-Van de…

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  • Oro-Dental Manifestations in a Pediatric Patient Affected by Helsmoortel-Van der Aa Syndrome

    Open Access•Massimo Petruzzi, Alessandro Stella et al.•ARTICLE•International Journal of…•2021

    Aim : Aim of this case report is to describe oro-facial abnormalities in a patient affected by Helsmoortel-Van der Aa syndrome, a rare autism syndrome, with not well described dental and cranial malformations. Case Report : Helsmoortel-Van der Aa Syndrome is a rare autosomal genetic syndrome causing mental impairment and autism, craniofacial dysmorphism, chest deformity and multiple organs dysfunction. Oro-facial involvement in Helsmoortel-Van de…

Medicine (1 work) · Neurogenetic and Muscular Disorders Research (1 work) · RNA modifications and cancer (1 work) · RNA regulation and disease (1 work)

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