Literature DB >> 21862914

Fanconi anemia with concurrent thumb polydactyly and dorsal dimelia: a case report with discussion of embryology.

M M Al-Qattan1.   

Abstract

Fanconi anemia is known to be associated with radial ray deficiency (thumb and radius hypoplasia), and its embryological basis remains to be poorly understood. We describe a rare case of Fanconi anemia with concurrent thumb polydactyly and dorsal dimelia. The embryological basis of limb abnormalities in Fanconi anemia patients is thought to be based on the complex interactions between the apical ectodermal ridge (where Fanconi anemia genes are expressed) and both the mesoderm (where Spalt-like 4 (SALL4) and Sonic hedgehog (SHH) are located and which are responsible for radial ray deficiency, thumb polydactyly, and triphalangism) and the dorsoventral axis (an error in that axis leads to dorsal dimelia).

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Year:  2013        PMID: 21862914     DOI: 10.1097/SAP.0b013e31822f9960

Source DB:  PubMed          Journal:  Ann Plast Surg        ISSN: 0148-7043            Impact factor:   1.539


  2 in total

1.  Fanconi Anemia Concurrent with an Unusual Thumb Polydactyly: A Case Report.

Authors:  Ahmadreza Afshar
Journal:  Arch Bone Jt Surg       Date:  2016-04

2.  Fanconi anaemia with bilateral diffuse pulmonary arterio venous fistulae: a case report.

Authors:  Lasitha Samarakoon; Nuwan Ranawaka; Chaturaka Rodrigo; Godwin R Constantine; Lalindra Goonarathne
Journal:  BMC Blood Disord       Date:  2012-03-17
  2 in total

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