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1.
J Child Neurol ; 16(10): 751-8, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11669349

RESUMO

Key features of Joubert syndrome include developmental delay, hypotonia, hyperpnea and apnea, oculomotor apraxia, and the presence of the molar tooth sign on axial imaging through the brainstem isthmus--the junction of the pons and mesencephalon. Interestingly, 1 in 10 patients with Joubert syndrome has abnormal cerebrospinal fluid collections misdiagnosed as Dandy-Walker variants. Because of important differences in patient management, genetic counseling, and prognosis between these conditions, we undertook a study to determine if the brainstem isthmus is normal in Dandy-Walker syndrome. Using standard landmarks, we evaluated development of the isthmus in normal subjects and in subjects with Joubert syndrome and Dandy-Walker syndrome. Four of five brainstem measures increased with age in normal subjects. In subjects with Joubert syndrome, the depth and length of the interpeduncular fossa were increased, and the width of the isthmus was decreased. In subjects with Dandy-Walker syndrome, the width of the brainstem isthmus was normal, and the molar tooth sign was absent. Although the pons can be hypoplastic in Dandy-Walker syndrome, we conclude that the pontomesencephalic junction is normal. Thus, the molar tooth sign can effectively distinguish between Joubert and Dandy-Walker syndromes. Genetic heterogeneity or epigenetic factors may account for abnormal cerebrospinal fluid collections in some cases of Joubert syndrome.


Assuntos
Tronco Encefálico/anormalidades , Síndrome de Dandy-Walker/diagnóstico , Deficiências do Desenvolvimento/diagnóstico , Imageamento por Ressonância Magnética , Hipotonia Muscular/diagnóstico , Malformações do Sistema Nervoso/diagnóstico , Adolescente , Apraxias/diagnóstico , Apraxias/genética , Tronco Encefálico/patologia , Criança , Pré-Escolar , Síndrome de Dandy-Walker/genética , Deficiências do Desenvolvimento/genética , Diagnóstico Diferencial , Feminino , Aconselhamento Genético , Humanos , Lactente , Masculino , Mesencéfalo/anormalidades , Mesencéfalo/patologia , Hipotonia Muscular/genética , Malformações do Sistema Nervoso/genética , Ponte/anormalidades , Ponte/patologia , Valores de Referência
2.
J Child Neurol ; 14(10): 642-8; discussion 669-72, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10511336

RESUMO

Children with Joubert syndrome have physical and intellectual disabilities. The purpose of this study was to assess the impact of Joubert syndrome on parental burden, coping, and family functioning. Forty-nine primary caregivers were surveyed. Forty-three primary caregivers were mothers and six were fathers; their mean age was 34 years. The following measures were used: Beck Depression Inventory, Child Development Inventory, Caregiver Strain Index, Family Assessment Device, and Ways of Coping Checklist-Revised. The data show that caregiver burden is not related to the severity of the child's illness, but that caregivers report significant burden. Higher burden was associated with the use of palliative coping methods, and family functioning was problematic. The results of this study suggest that for parents of children with Joubert syndrome, degree of parental burden depends more on the parents' coping skills and the level of family functioning rather than on the degree of the child's impairment. These findings highlight the importance of assessing caregiver burden, as well as decreased family functioning or coping abilities, since these problems often can be managed with psychologic intervention.


Assuntos
Adaptação Psicológica , Cuidadores/psicologia , Cerebelo/anormalidades , Efeitos Psicossociais da Doença , Deficiências do Desenvolvimento/psicologia , Relações Familiares , Ataxias Espinocerebelares/psicologia , Atividades Cotidianas/psicologia , Adolescente , Criança , Pré-Escolar , Deficiências do Desenvolvimento/genética , Feminino , Humanos , Lactente , Masculino , Ataxias Espinocerebelares/genética , Síndrome
3.
J Fla Med Assoc ; 84(8): 510-4, 1997 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-9401348

RESUMO

Academic medical centers have been restructuring faculty compensation plans because decreasing clinical revenues have created budgetary problems. We propose an overall compensation strategy designed to reward high performance of university physicians. The approach incorporates Management by Objectives to improve communication of expectations within the organization and provide college of medicine leadership with much needed mechanisms to align faculty compensation with productivity.


Assuntos
Médicos/economia , Salários e Benefícios , Faculdades de Medicina/economia , Centros Médicos Acadêmicos/economia , Centros Médicos Acadêmicos/organização & administração , Orçamentos , Comunicação , Eficiência , Eficiência Organizacional , Docentes de Medicina/organização & administração , Objetivos , Humanos , Renda , Liderança , Objetivos Organizacionais , Faculdades de Medicina/organização & administração , Gestão da Qualidade Total
4.
J Neurooncol ; 30(3): 199-211, 1996 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-8943095

RESUMO

Cell motility within central nervous system (CNS) neuropil may be largely restricted yet infiltration by glioma cells is commonly observed. Glioma cells remodel nervous tissue and may assemble extracellular matrix in order to migrate. We examined the rat C6 glioma cell line for laminin expression and response in vitro and following engraftment into rat spinal cord. C6 cell cultures expressed laminin-2. C6 cells attached equally well to substrates of purified laminin-1 and laminin-2 and laminin-2-enriched C6 conditioned medium. In contrast, C6 cell migration was substantially greater on laminin-2 and C6-derived substrata than on laminin-1. Glioma cell attachment to laminin-1 and -2 was largely inhibited by antibody to the laminin receptor LBP110 and by an IKVAV peptide but not by YIGSR or control peptides. IKVAV peptide and anti-LBP110 antibodies also inhibited glioma cell invasion through synthetic basement membrane. Anti-beta 1 integrin antibody selectively inhibited cell migration and invasion on laminin-2 substrata without affecting percent cell attachment. These findings suggest C6 cell migration and invasion are promoted by autocrine release of laminin-2 and involve LPB110 and beta 1 integrin laminin receptors. A possible role for laminin-2 in CNS infiltration in vivo was examined following glioma engraftment into rat spinal cord. Engrafted C6 tumors share many histologic features of invasive human glioma. Engrafted glioma cells expressed laminin, LBP110 and beta 1 integrin antigens, indicating the molecular mechanisms of C6 motility observed in culture may contribute to glioma invasion in vivo. NMR and corroborative immunocytochemistry provided precise means to monitor tumor progression following glioma engraftment into rat spinal cord. Advantages of this glioma model are discussed regarding the assessment of anti-adhesive therapies in vivo.


Assuntos
Glioma/patologia , Laminina/farmacologia , Neoplasias da Medula Espinal/patologia , Animais , Western Blotting , Bromodesoxiuridina , Proteínas de Transporte/análise , Proteínas de Transporte/biossíntese , Adesão Celular/fisiologia , Movimento Celular/fisiologia , Modelos Animais de Doenças , Imuno-Histoquímica , Integrina beta1/análise , Integrina beta1/biossíntese , Laminina/análise , Laminina/metabolismo , Espectroscopia de Ressonância Magnética , Camundongos , Microinjeções , Invasividade Neoplásica , Transplante de Neoplasias , Fibras Nervosas/química , Fibras Nervosas/metabolismo , Fibras Nervosas/patologia , Proteínas do Tecido Nervoso/análise , Proteínas do Tecido Nervoso/biossíntese , Neuroglia/química , Neuroglia/metabolismo , Neuroglia/patologia , Ratos , Neoplasias da Medula Espinal/metabolismo , Células Tumorais Cultivadas/citologia , Células Tumorais Cultivadas/efeitos dos fármacos , Células Tumorais Cultivadas/transplante
5.
Artigo em Inglês | MEDLINE | ID: mdl-7950012

RESUMO

The treatment of brain tumors requires a large team of medical experts. However, the process of medical decision-making for these patients is hampered by the frequent inaccessibility of the experts because of conflicting scheduling, inconsistencies in the management of different patients, and the fact that multiple experts often yield multiple opinions. The goals of this work were (1) to develop and validate an expert system to assist the medical team deliver efficient, quality care to children with recurrent medulloblastoma, a common type of pediatric brain tumor, and (2) to determine if the expert system can be used as an educational tool. The results of our study indicate that residents enjoy learning by using XNEOr, the brain tumor expert system. XNEOr enabled residents to order appropriate ancillary tests for patients and to make fewer incorrect treatment decisions. The potential net effect of residents using XNEOr may be increased patient and family satisfaction and decreased probability of medical liability. At a time of important changes in our health care system, novel expert systems hold promise as tools to reduce medical costs, improve the quality of multi-expert medical care, and advance health care education.


Assuntos
Neoplasias Encefálicas , Instrução por Computador , Tomada de Decisões Assistida por Computador , Sistemas Inteligentes , Oncologia , Meduloblastoma , Neoplasias Encefálicas/diagnóstico , Neoplasias Encefálicas/terapia , Criança , Sistemas Computacionais , Estudos de Avaliação como Assunto , Humanos , Internato e Residência , Oncologia/economia , Oncologia/educação , Meduloblastoma/diagnóstico , Meduloblastoma/terapia , Equipe de Assistência ao Paciente , Qualidade da Assistência à Saúde , Radioterapia Assistida por Computador
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