Pedro Henrique Ribeiro Moreira

CV Lattes ResearcherID ORCID

Universidade de São Paulo (USP). Hospital de Reabilitação de Anomalias Craniofaciais (HRAC) (Institutional affiliation from the last research proposal)
Birthplace: Brazil

Has experience in Medicine, focusing on Medicine (Source: Lattes Curriculum)

News published in Agência FAPESP Newsletter about the researcher

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TITULO

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VEICULO: TITULO (DATA)

Scholarships in Brazil

Completed (most recent)

Abstract
Introduction: The velocardiofacial spectrum syndrome, often caused by the 22q11.2 deletion, affects one in every 2,000 individuals, which makes it one of the most frequent syndromes in humans. Among more than 180 findings present in the spectrum of chromosome 22q11.2 alterations, congenital heart diseases and craniofacial anomalies stands out, in addition to sleep-disordered breathing, wh…
Analysis of the prevalence of sleep-disordered breathing in individuals with velocardiofacial spectrum syndrome and relationship with cardiorespiratory capacity, BP.IC

Virtual Library in numbers * Updated data on August 23, 2025

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1 / 1	Completed scholarships in Brazil

Associated processes

Most frequent collaborators in research granted by FAPESP

Sergio Henrique Kiemle Trindade

Keywords used by the researcher

Health Sciences Medicine

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Abstract