| Autor: |
da Silva Lima, Victor Fernando, Tenório Pinto, Bruna Assis, Leite Nelson, Claudia Bem, Medeiros Campos, Eduarda, Pacheco Gonsioroski, Lucas, dos Santos Souza, Mariana Rodrigues, Chaves de Siqueira, Rayza Cecília, de Araújo Vilarim, José Nivaldo |
| Zdroj: |
Brazilian Journal of Mother & Child Health (BJMCH) / Revista Brasileira de Saude Materno Infantil (RBSMI); 2023, Vol. 23, p1-6, 6p |
| Abstrakt: |
Introduction: goldenhar syndrome is a rare congenital syndrome that affects the craniofacial morphogenesis. It is a complex syndrome, with heterogeneous presentation which the diagnosis can still be performed in the intrauterine through morphological ultrasound. Description: a case report of a 4-year-old male patient diagnosed with Goldenhar syndrome, along with its clinical presentation, diagnostic investigation and follow-up. Discussion: the follow-up on these patients remains a challenge, since it can affect different systems and with different presentations. The earlier the diagnosis is performed, the greater the patient's chances of having a favorable prognosis with multidisciplinary stimulation. The objective of this article is to contribute to the medical literature, in order to assist in the diagnosis and management of future cases. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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