Diagnóstico tardio de síndrome de deleção 22q11.2 em criança com hipocalcemia sintomática: relato de caso

• Main Authors: Camila Dalle Rocha (Author), Maisa Andressa Sohn (Author), Felipe Augusto Moreschi (Author), Daniel Almeida do Valle (Author), Mara Lúcia Schmitz Ferreira Santos (Author), Vitor Costa Palazzo (Author)
• Format: Book
• Published: Sociedade Brasileira de Pediatria, 2023-09-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

22q11.2 Deletion Syndrome is the commonest microdeletion syndrome in humans and has a wide spec-trum of clinical manifestations, such as craniofacial dysmorphism, airway malformations, heart disease, renal malformations, hypoparathyroidism, neurological and behavioral disorders, immunodeficiencies a...