Hereditary coproporphyria with acute intermittent manifestations.
Rattachement africain : dk, fi, gb, us. Niveau de preuve : code pays fourni par la source.
Le résumé fourni par la source
Cytomegalovirus-Klemnola and Kaariaiinen *ME JRsH established during the disease in four previously healthy adults and one child with a mononucleosis-like disease without a positive heterophil agglutination test.No antibodies were demonstrable in the first sample from three patients.The disease was characterized by protracted fever and absence of tonsillitis.Enlargement of the lymph nodes was seen in only one patient.The tests for liver function gave abnormal results in all the cases.Leucocytosis, relative and absolute lymphocytosis, and the appearance of abundant atypical lymphocytes were features of the haernatological pattern.No significant rise of the C.F. antibody titre to the cyto- megalovirus was demonstrable in a single case among 19 patients suffering from infectious mononucleosis with a positive heterophil agglutination test or among 130 patients with various acute infectious diseases.A high titre, however, was found in two patients with infectious mononucleosis, there being a significant decrease of the titre later, after the disease was over, and in two patients of the control material, both of whom had a chronic debilitating disease in addition to their acute infection.We are indebted to Dr.
Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.
Le contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.
- Titre Crossref
- Hereditary coproporphyria with acute intermittent manifestations.
- Date Crossref
- 06/11/1965
- Éditeur
- BMJ
- Type
- journal-article
Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.
Les institutions déclarées
Une affiliation ne permet pas de déduire la nationalité d’un auteur.