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Ehlers-Danlos Syndrome (EDS) is a group of connective tissue disorders that affect the skin, joints, and blood vessel walls.

Giorni lavorativi10

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Specifiche

Razza

Gene

Cromosoma

D4

Mutation

c.112_118+15del

Tipo di Ereditarietà

Autosomica Dominante

Organo

Campione

Tampone, Sangue in EDTA, Sangue in Eparina, Seme, Tessuto

Also known as

cEDS

Informazioni generali

Ehlers-Danlos Syndrome (EDS) is a group of connective tissue disorders that affect the skin, joints, and blood vessel walls. The condition results from defects in the synthesis and structure of collagen, which is a crucial protein for the strength and elasticity of connective tissue. An autosomal dominant mutation in the collagen, type V, alpha 1 (COL5A1) gene lead to Type 1 EDS. This is also known as Classical EDS (cEDS) or Feline cutaneous asthenia and is one of the most common forms which is characterized by hyper-elastic skin and joint hypermobility. This variant tested for is specific for the Bengal breed.

Caratteristiche cliniche

The collagen fibers in cats with EDS Type 1 have an abnormal structure which means the skin is friable and fragile and prone to damage. The skin is weaker, and its structural properties are reduced leading to laxity of joints, poor wound healing and abnormal scarring. The collagen deficiency also affects other tissues in the body, including the heart, blood vessels, and eyes. The combination of fragile skin and weaker blood vessels can lead to bruises or hematomas under the skin or swelling around joints.

Symptoms can develop within a few hours to a maximum of several months after birth. Cats with mild EDS have a normal live expectancy, although they are at high risk of skin injuries and constant management of wounds is required.

Informazioni aggiuntive

Riferimenti

Pubmed ID: 35627182

Year published: 2022

Omia ID: 2165

Omia variant ID: 1464

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