A Review of the Genetics and Pathogenesis of Syndactyly in Humans and Experimental Animals: A 3-Step Pathway of Pathogenesis

Author

al-Qattan, Mohammad M.

Source

BioMed Research International

Issue

Vol. 2019, Issue 2019 (31 Dec. 2019), pp.1-10, 10 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2019-09-15

Country of Publication

Egypt

No. of Pages

10

Main Subjects

Medicine

Abstract EN

Embryology of normal web space creation and the genetics of syndactyly in humans and experimental animals are well described in the literature.

In this review, the author offers a 3-step pathway of pathogenesis for syndactyly.

The first step is initiated either by the overactivation of the WNT canonical pathway or the suppression of the Bone Morphogenetic Protein (BMP) canonical pathway.

This leads to an overexpression of Fibroblast Growth Factor 8 (FGF8).

The final step is the suppression of retinoic acid in the interdigital mesenchyme leading to suppression of both apoptosis and extracellular matrix (ECM) degradation, resulting in syndactyly.

American Psychological Association (APA)

al-Qattan, Mohammad M.. 2019. A Review of the Genetics and Pathogenesis of Syndactyly in Humans and Experimental Animals: A 3-Step Pathway of Pathogenesis. BioMed Research International،Vol. 2019, no. 2019, pp.1-10.
https://search.emarefa.net/detail/BIM-1128732

Modern Language Association (MLA)

al-Qattan, Mohammad M.. A Review of the Genetics and Pathogenesis of Syndactyly in Humans and Experimental Animals: A 3-Step Pathway of Pathogenesis. BioMed Research International No. 2019 (2019), pp.1-10.
https://search.emarefa.net/detail/BIM-1128732

American Medical Association (AMA)

al-Qattan, Mohammad M.. A Review of the Genetics and Pathogenesis of Syndactyly in Humans and Experimental Animals: A 3-Step Pathway of Pathogenesis. BioMed Research International. 2019. Vol. 2019, no. 2019, pp.1-10.
https://search.emarefa.net/detail/BIM-1128732

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1128732