Diagnóstico tardio de síndrome de deleção 22q11.2 em criança com hipocalcemia sintomática: relato de caso
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...
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| Үндсэн зохиолчид: | , , , , , |
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| Формат: | Artigo |
| Хэл сонгох: | Inglês |
| Хэвлэсэн: |
Sociedade Brasileira Pediatria
2023-09-01
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| Цуврал: | Residência Pediátrica |
| Нөхцлүүд: | |
| Онлайн хандалт: | https://residenciapediatrica.com.br/detalhes/1412/diagnostico%20tardio%20de%20sindrome%20de%20delecao%2022q11-2%20em%20crianca%20com%20hipocalcemia%20sintomatica-%20relato%20de%20caso |
| Шошгууд: |
Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!
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