Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Minerva Pediatr ; 44(11): 573-5, 1992 Nov.
Artigo em Italiano | MEDLINE | ID: mdl-1297925

RESUMO

The Authors describe a case of neonatal hemorrhagic syndrome associated with a large hemangioma on the left lower limb with an unfavourable prognosis. The clinical, biohumoral and anatomicopathological characteristics indicate a Kasabach-Merrit syndrome (SKM) with massive platelet sequestration in the large hemangioma. The pathogenetical mechanisms of SKM and the medical surgical and radiant therapy are mentioned. The Authors also discuss the various diagnostic problems imposed by the presence of serious hemorrhagic pathology at neonatal age.


Assuntos
Hemangioma/diagnóstico , Parada Cardíaca/etiologia , Hemangioma/sangue , Hemangioma/complicações , Humanos , Recém-Nascido , Masculino , Prognóstico , Trombocitopenia/complicações
2.
Minerva Pediatr ; 44(9): 451-4, 1992 Sep.
Artigo em Italiano | MEDLINE | ID: mdl-1474974

RESUMO

The Authors describe a case of CHARGE association (CA) with fibrocystic disease of the pancreas (FCP). The CA is characterized by seven mayor defects (colobomatous malformation, heart defect, atresia choanae, growth and mental deficiency, genital hypoplasia, ear anomalies and/or deafness). Four of this seven defects are necessary for the diagnosis. Other diseases and anomalies associated with CA are examined. The peculiarity of contemporaneous presence of FCP and the seriousness of the prognosis is pointed out.


Assuntos
Anormalidades Múltiplas , Fibrose Cística/complicações , Humanos , Recém-Nascido , Masculino , Síndrome
3.
Minerva Pediatr ; 44(7-8): 361-4, 1992.
Artigo em Italiano | MEDLINE | ID: mdl-1406510

RESUMO

The Authors describe an uncommon case of growth retardation; the clinical and radiological elements that the Authors to a diagnosis of spondyloepiphyseal dysplasia (SED) are noted; they compare this to other diagnosis of different types of growth retardation, they underline the necessity of taking these rare types into consideration before undergoing diagnostic procedures that would be costly both to the patient and society.


Assuntos
Osteocondrodisplasias , Criança , Diagnóstico Diferencial , Transtornos do Crescimento/diagnóstico , Humanos , Masculino , Osteocondrodisplasias/diagnóstico , Osteocondrodisplasias/diagnóstico por imagem , Radiografia
7.
Nat New Biol ; 246(153): 157-8, 1973 Dec 05.
Artigo em Inglês | MEDLINE | ID: mdl-4519147
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA