Article ID Journal Published Year Pages File Type
2202652 Seminars in Cell & Developmental Biology 2014 12 Pages PDF
Abstract

•Up-to-date summary of human genetic disorders associated with abnormalities in hair follicle morphogenesis, structure or regeneration.•Genetic basis of human hair disorders: atrichia, hypotrichosis, hypertrichosis and alterations in hair structure.•Spatial-temporal specificity of human hair defects.

Mouse models have greatly helped in elucidating the molecular mechanisms involved in hair formation and regeneration. Recent publications have reviewed the genes involved in mouse hair development based on the phenotype of transgenic, knockout and mutant animal models. While much of this information has been instrumental in determining molecular aspects of human hair development and cycling, mice exhibit a specific pattern of hair morphogenesis and hair distribution throughout the body that cannot be directly correlated to human hair. In this mini-review, we discuss specific aspects of human hair follicle development and present an up-to-date summary of human genetic disorders associated with abnormalities in hair follicle morphogenesis, structure or regeneration.

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Life Sciences Biochemistry, Genetics and Molecular Biology Cell Biology
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