Súlyos kombinált immundeficiencia korai felismerése és eredményes kezelése.

Translated title of the contribution: Early recognition and successful treatment of an infant with severe combined immune deficiency

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Abstract

A male infant of three month presented with recurrent mucosal and fungal infections, diarrhoea and failure to thrive from the age of three weeks. Laboratory test revealed T-B-NK + severe combined immunodeficiency (SCID). Family history and immunolaboratory findings suggested autosomal recessive form of the disease. Haploidentical maternal bone marrow transplantation (BMT) was carried out at five and half months of age. Over the two years after BMT, the patient's somatomotoric and mental development is normal. Cellular immune responses and the substantial immunoglobulin production suggest immunoreconstruction in the child born with complete lack of adaptive immunity. According to the author's knowledge, this is the first T-B-NK + patient in Hungary, whose disease was diagnosed and adequately treated in infancy.

Translated title of the contributionEarly recognition and successful treatment of an infant with severe combined immune deficiency
Original languageHungarian
Pages (from-to)2081-2083
Number of pages3
JournalOrvosi hetilap
Volume143
Issue number36
Publication statusPublished - Sep 8 2002

ASJC Scopus subject areas

  • Medicine(all)

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