A csontvelöelégtelenség ritka, veleszületett formái.

Translated title of the contribution: Rare congenital forms of bone marrow deficiency

T. Révész, G. Kardos, D. Schuler

Research output: Contribution to journalArticle

Abstract

Cases of rare congenital forms of aplastic anaemia are presented. Fanconi anaemia is most frequently diagnosed, while reticular dysgenesis, amegakaryocytic thrombocytopenia and dyskeratosis congenita occur exceptionally rarely. A presumably new entity of congenital aplastic anaemia called "RAC" syndrome (retinopathy--aplastic anaemia--central nervous system abnormalities) is presented too. A short summary of the pathomechanism of congenital aplastic anaemias and present therapeutic attempts, including the possible therapeutic use of the newly discovered stem cell factor are described.

Original languageHungarian
Pages (from-to)1147-1150
Number of pages4
JournalOrvosi Hetilap
Volume134
Issue number21
Publication statusPublished - May 23 1993

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Aplastic Anemia
Bone Marrow
Dyskeratosis Congenita
Nervous System Malformations
Fanconi Anemia
Stem Cell Factor
Therapeutic Uses
Thrombocytopenia
Central Nervous System
Therapeutics

ASJC Scopus subject areas

  • Medicine(all)

Cite this

A csontvelöelégtelenség ritka, veleszületett formái. / Révész, T.; Kardos, G.; Schuler, D.

In: Orvosi Hetilap, Vol. 134, No. 21, 23.05.1993, p. 1147-1150.

Research output: Contribution to journalArticle

Révész, T, Kardos, G & Schuler, D 1993, 'A csontvelöelégtelenség ritka, veleszületett formái.', Orvosi Hetilap, vol. 134, no. 21, pp. 1147-1150.
Révész T, Kardos G, Schuler D. A csontvelöelégtelenség ritka, veleszületett formái. Orvosi Hetilap. 1993 May 23;134(21):1147-1150.
Révész, T. ; Kardos, G. ; Schuler, D. / A csontvelöelégtelenség ritka, veleszületett formái. In: Orvosi Hetilap. 1993 ; Vol. 134, No. 21. pp. 1147-1150.
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