Apert's syndrome skull abnormalities, brain malformations, neuropsychological evaluation and timing for surgery (2001)
- Authors:
- USP affiliated authors: LAURIS, JOSÉ ROBERTO PEREIRA - FOB ; ABRAMIDES, DAGMA VENTURINI MARQUES - HRAC ; ZANINI, SILVIO ANTONIO - HRAC ; FERNANDES, ADRIANO YACUBIAN - FM
- Unidades: FOB; HRAC; FM
- Subjects: MALFORMAÇÕES; ANORMALIDADES CRANIOFACIAIS; CRANIOSSINOSTOSE
- Language: Inglês
- Abstract: Background: Apert syndrome is charactenzed by severe craniosynostosis, midface hypoplasia and symmetric syndactyly of the hands and sometimes of the feet The factors involved in the mental development of these patients are still in discussion. Methods: In the present study, 34 patients had diagnosis of Apert syndrome and 18 were completely studied with 3D-tomography and magnetic resonance of the brain, neuropsycological and social evaluation and had an interdisciplinary treattment. Results: Ventriculomegaly (5), hypoplasia of corpus callosun (5), hypoplasia of septum pellucidum (5), cavum vergae of septum pellucidum (2) and arachnoid Cyst of the posterior fossa (2) was observed. Morphologic measurements of the corpus callosum was established and associated wilh the type of the surgery (p=0,012). the intelligence quotient (IQ) was obtained (average = 74 (45 to 108)). IQ was greater than 69 in 66% of patients and the factors associated with mental development were quality of the family environment (p=O,O 19) and brain malformation (p=0,068). Age at operation was not correlated to the lQ. Conclusion: Morphologic measurements of the corpus callosum is an evidence of the changes in the disposal of the brain struclures after surgery Quality of the family environment was the most significant factor involved in the final lQ of the patients with Apert syndrome.
- Imprenta:
- Publisher: World Federation of Neurosurgical Societies
- Publisher place: Sydney
- Date published: 2001
- Source:
- Título: Proceeedings
- Conference titles: World Congress of Neurosugery
-
ABNT
FERNANDES, Adriano Yacubian et al. Apert's syndrome skull abnormalities, brain malformations, neuropsychological evaluation and timing for surgery. 2001, Anais.. Sydney: World Federation of Neurosurgical Societies, 2001. Disponível em: https://repositorio.usp.br/directbitstream/0b71bbe5-6f1d-473f-82ef-04c6904c73b4/1229413.PDF. Acesso em: 14 mar. 2026. -
APA
Fernandes, A. Y., Palhares, A., Giglio, A., Gabarra, R. C., Perosa, G. B., Abramides, D. V. M., et al. (2001). Apert's syndrome skull abnormalities, brain malformations, neuropsychological evaluation and timing for surgery. In Proceeedings. Sydney: World Federation of Neurosurgical Societies. Recuperado de https://repositorio.usp.br/directbitstream/0b71bbe5-6f1d-473f-82ef-04c6904c73b4/1229413.PDF -
NLM
Fernandes AY, Palhares A, Giglio A, Gabarra RC, Perosa GB, Abramides DVM, Zanini SA, Portela L, Lauris JRP, Plese JPP. Apert's syndrome skull abnormalities, brain malformations, neuropsychological evaluation and timing for surgery [Internet]. Proceeedings. 2001 ;[citado 2026 mar. 14 ] Available from: https://repositorio.usp.br/directbitstream/0b71bbe5-6f1d-473f-82ef-04c6904c73b4/1229413.PDF -
Vancouver
Fernandes AY, Palhares A, Giglio A, Gabarra RC, Perosa GB, Abramides DVM, Zanini SA, Portela L, Lauris JRP, Plese JPP. Apert's syndrome skull abnormalities, brain malformations, neuropsychological evaluation and timing for surgery [Internet]. Proceeedings. 2001 ;[citado 2026 mar. 14 ] Available from: https://repositorio.usp.br/directbitstream/0b71bbe5-6f1d-473f-82ef-04c6904c73b4/1229413.PDF - Síndrome de Crouzon: fatores envolvidos no desenvolvimento neuropsicologico e na qualidade de vida
- Syndromic craniosynostosis: neuropsycholinguistic abilities and imaging analysis of the central nervous system
- Histological and radioisotopical analysis of the skull graft: an experimental study in rabbits
- Reconstruction of the anterior cranial floor with bone grafts
- Cirurgia craniofacial: malformações
- Coloboma treatment in treacher collins syndrome
- Bone graft of the zygoma in a patient with Treacher-Collins syndrome
- A craniofacial classification of the meningoceles
- Facial bone lengthening apparatus with expander and miniplates
- Condições e benefícios das cirurgias craniofacias no HRAC/USP
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
1229413.PDF |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
