Congenital thrombocytopenia and radio-ulnar synostosis: A new familial syndrome

Alexis A. Thompson*, Kelly Woodruff, Stephen A. Feig, Long T. Nguyen, N. Carolyn Schanen

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

71 Scopus citations

Abstract

The association of bone marrow failure and skeletal defects has been frequently noted, however, the genetic basis for most of these syndromes remains unclear. We describe a previously uncharacterized autosomal dominant syndrome of amegakaryocytic thrombocytopenia associated with radial-ulnar synostosis. The clinical features of this syndrome appear to be distinct from other similar conditions, including Fanconi's anaemia and thrombocytopenia-absent radii (TAR). The physical findings at diagnosis and clinical management of each case are detailed, as well as a discussion of this disorder in the context of other syndromes in which marrow failure and skeletal defects are prominent features. We also review recent developments in molecular genetics that may provide important clues to the underlying aetiology of this condition.

Original languageEnglish (US)
Pages (from-to)866-870
Number of pages5
JournalBritish Journal of Haematology
Volume113
Issue number4
DOIs
StatePublished - 2001

Keywords

  • Amegakaryocytic thrombocytopenia
  • Marrow failure
  • Radio-ulnar synostosis
  • Skeletal defects
  • Thrombocytopenia

ASJC Scopus subject areas

  • Hematology

Fingerprint

Dive into the research topics of 'Congenital thrombocytopenia and radio-ulnar synostosis: A new familial syndrome'. Together they form a unique fingerprint.

Cite this