Thrombasthenia in Iraqi Jews

N. Reichert, U. Seligsohn, B. Ramot

Research output: Contribution to journalArticlepeer-review

Abstract

Glanzmann's thrombasthenia is an extremely rare hemostatic disorder characterized by a severe lifelong bleeding tendency, prolonged bleeding time, impaired clot retraction and failure of the platelets to aggregate with high concentrations of ADP. A recent survey on this disorder in the major Israeli medical centers revealed 19 cases in the Iraqi Jewish community (total population about 240,000). Pedigree analysis shows that thrombasthenia is an autosomal recessive disorder.

Original languageEnglish
Pages (from-to)1406
Number of pages1
JournalIsrael Journal of Medical Sciences
Volume9
Issue number9-10
StatePublished - 1973
Externally publishedYes

Fingerprint

Dive into the research topics of 'Thrombasthenia in Iraqi Jews'. Together they form a unique fingerprint.

Cite this