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Craniosynostosis - Recognition, clinical characteristics, and treatment.
Kajdic, Nina; Spazzapan, Peter; Velnar, Tomaz.
Afiliação
  • Kajdic N; Chair of Surgery, Medical Faculty, University of Ljubljana, Ljubljana, Slovenia. nkajdic@gmail.si.
Bosn J Basic Med Sci ; 18(2): 110-116, 2018 May 20.
Article em En | MEDLINE | ID: mdl-28623672
Craniosynostosis is a developmental craniofacial anomaly, resulting in impairment of brain development and abnormally shaped skull. The main cause of craniosynostosis is premature closure of one or more cranial sutures. It usually occurs as an isolated condition, but may also be associated with other malformations as part of complex syndromes. When left untreated, craniosynostosis can cause serious complications, such as developmental delay, facial abnormality, sensory, respiratory and neurological dysfunction, anomalies affecting the eye, and psychological disturbances. Thus, early diagnosis, expert surgical techniques, postoperative care, and adequate follow-up are of vital importance in treating craniosynostosis.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Encéfalo / Craniossinostoses Tipo de estudo: Prevalence_studies / Risk_factors_studies / Screening_studies Limite: Humans / Infant / Newborn Idioma: En Revista: Bosn J Basic Med Sci Assunto da revista: MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Eslovênia

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Encéfalo / Craniossinostoses Tipo de estudo: Prevalence_studies / Risk_factors_studies / Screening_studies Limite: Humans / Infant / Newborn Idioma: En Revista: Bosn J Basic Med Sci Assunto da revista: MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Eslovênia