Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans

Title:Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans

Volume: 16 Issue: 4

Author(s): Amira Elmakky, Ilaria Stanghellini, Antonio Landi and Antonio Percesepe

Affiliation:

Keywords: Radial deficiency, Congenital upper limb anomalies, Thumb hypoplasia.

Abstract: Radial deficiencies (RDs), defined as under/abnormal development or absence of any of the structures of the forearm, radial carpal bones and thumb, occur with a live birth incidence ranging from 1 out of 30,000 to 1 out 6,000 newborns and represent about one third/one fourth of all the congenital upper limb anomalies. About half of radial disorders have a mendelian cause and pattern of inheritance, whereas the remaining half appears sporadic with no known gene involved. In sporadic forms certain anomalies, such as thumb or radial hypoplasia, may occur either alone or in association with systemic conditions, like vertebral abnormalities or renal defects. All the cases with a mendelian inheritance are syndromic forms, which include cardiac defects (in Holt-Oram syndrome), bone marrow failure (in Fanconi anemia), platelet deficiency (in thrombocytopenia-absent-radius syndrome), ocular motility impairment (in Okihiro syndrome). The genetics of radial deficiencies is complex, characterized by genetic heterogeneity and high inter- and intra-familial clinical variability: this review will analyze the etiopathogenesis and the genotype/phenotype correlations of the main radial deficiency disorders in humans.

Cite this article as:

Elmakky Amira, Stanghellini Ilaria, Landi Antonio and Percesepe Antonio, Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans, Current Genomics 2015; 16 (4) . https://dx.doi.org/10.2174/1389202916666150528000412