Dubowitz syndrome
1998-02-01 Jean-Loup Huret  , Claude Léonard   AffiliationGenetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers France
Identity
Name
Dubowitz syndrome
Note
Dubowitz syndrome may be confused with Bloom syndrome; , another differential diagnosis is fetal alcohol syndrome
Inheritance
autosomal recessive; heterogeneity cannot be excluded; less than 150 cases described
Omim
223370
Mesh
C535718
Orphanet
235 Dubowitz syndrome
Umls
C0175691
Clinics
Note
phenotypic spectrum variable
Phenotype and clinics
Neoplastic risk
haematological malignancies and pancytopenia in 10%, childhood myelodysplasia in particular; lymphomas
Cytogenetics
Inborn condition
appears to be normal or near to normal in most cases, although an increased rate of chromosomal breakage has also been descibed
To be noted
Associations
http:\/\/www.dubowitz.org Dubowitz syndrome
Article Bibliography
| Pubmed ID | Last Year | Title | Authors |
|---|---|---|---|
| 8723121 | 1996 | Dubowitz syndrome: review of 141 cases including 36 previously unreported patients. | Tsukahara M et al |
External Links
Citation
Jean-Loup Huret ; Claude Léonard
Dubowitz syndrome
Atlas Genet Cytogenet Oncol Haematol. 1998-02-01
Online version: http://atlasgeneticsoncology.org/cancer-prone-disease/10016/dubowitz-syndrome/
