Amegakaryocytic Thrombocytopenia with Radio-Ulnar Synostosis (ATRUS): A Case Report
Sachin Bansal, Pradeep Kumar, Ipsita Sahoo, Rajesh Kashyap, Pritish Chandra Patra
Asian Hematology Research Journal · pp. 113–116 · Published 12 Aug 2020
Abstract
The association of bone marrow failure and skeletal defects is well known. However, the genetic basis for most of these syndromes remains unclear. We describe here a syndrome of congenital amegakaryocytic thrombocytopenia (CAMT) with skeletal abnormality. This case report summarizes the clinical presentation of an infant with anemia and thrombocytopenia in which the basic work up has led to the diagnosis of ATRUS.
Cited by 0
No indexed citations yet.
Article metrics
Real usage data collected on this platform.
0
Page views
0
PDF downloads
0
Outbound clicks
0
Citations
Views by country
Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".
No views recorded yet.
Traffic sources
Referring site, by host.
No traffic recorded yet.
Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.