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Ehlers Danlos Syndrome Symptoms In Children

Child S Life With Eds

Child S Life With Eds

Ehlers danlos syndrome symptoms in children. Spondylodysplastic EDS spEDS characterized by short stature progressive in childhood muscle hypotonia ranging from severe congenital to mild later-onset and bowing of limbs. There are 14 types of EDS and all except one have a known specific genetic cause. Symptoms and signs of Ehlers-Danlos syndrome vary widely.

Joint dislocates or separates called subluxation with mild trauma. Typical symptoms include flexible joints a humpback flat feet and elastic skin. Common symptoms include.

Desmopressin has been described in case reports to decrease bleeding times in these patients. Patients with Ehlers-Danlos will have a variety of symptoms including but not limited to joint pain cardiac symptoms GI problems dysautonomia and autoimmune symptoms. It is generally considered the least severe form of Ehlers-Danlos syndrome EDS although significant complications can occur.

Some of the more common symptoms children with EDS complain of include. Their skin is stretchy and fragile. Pediatric EDS symptoms can appear at birth or soon afterward and can include abnormal scarring autonomic nervous system issues cardiovascular problems early-onset osteoarthritis elastic or stretchy skin that bruises easily extra folds of skin gastrointestinal issues internal bleeding joint hypermobility organ rupture osteoporosis bleeding and sometimes velvety skin.

This syndrome is caused by a defect in one of the genes that control the production of connective tissue. They cause the skin to become elastic or stretchy. Pain that first appears as growing pains in young children but can become more widespread and chronic in teens and older people.

It is not uncommon for a genetic condition to first become apparent during puberty alternatively symptoms can be triggered by a trauma such as a virus many years down the line. People with Ehlers-Danlos syndrome or EDS have very loose hypermobile joints. The signs and symptoms of Ehlers-Danlos syndrome vary depending on the type of disorder and can range from mild to life threatening.

Predominant symptoms include hypermobile joints abnormal scar formation and wound healing fragile vessels and velvety hyperextensible skin. Ehlers-Danlos syndrome EDS is not a single syndrome but rather a group of conditions that affect connective tissue such as the skin bones cartilage tendons blood vessels and more.

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Pediatric EDS symptoms can appear at birth or soon afterward and can include abnormal scarring autonomic nervous system issues cardiovascular problems early-onset osteoarthritis elastic or stretchy skin that bruises easily extra folds of skin gastrointestinal issues internal bleeding joint hypermobility organ rupture osteoporosis bleeding and sometimes velvety skin.

The signs and symptoms of Ehlers-Danlos syndrome vary depending on the type of disorder and can range from mild to life threatening. The signs and symptoms of Ehlers-Danlos syndrome vary depending on the type of disorder and can range from mild to life threatening. However Ehlers-Danlos syndrome is a complex illness and can cause many serious physical issues beyond simply being flexible In order to better understand the different ways in which EDS can affect people we asked our Mighty community to share some of the physical symptoms of Ehlers-Danlos syndrome that surprised them. A lot of children with EDS are mild and their symptoms might go unnoticed. Typical symptoms include flexible joints a humpback flat feet and elastic skin. Patients with Ehlers-Danlos will have a variety of symptoms including but not limited to joint pain cardiac symptoms GI problems dysautonomia and autoimmune symptoms. Pain is caused by the overall joint instability. Desmopressin has been described in case reports to decrease bleeding times in these patients. Their skin is stretchy and fragile.


Hypermobility in the hands fingers and toes. Ehlers-Danlos Syndrome EDS is caused by heritable collagen defects and may be associated with bleeding symptoms. EDS is most commonly autosomal dominant and associated with joint laxity skin hyperelasticity delayed wound healing and fragility of tissues and blood vessels with easy bruisability in 90 of patients Nuss MancoJohnson 1995. Ehlers-Danlos syndrome is a group of disorders that affect the connective tissues that comprise a childs skin bones blood vessels and other areas of the body. Common symptoms include. It is not uncommon for a genetic condition to first become apparent during puberty alternatively symptoms can be triggered by a trauma such as a virus many years down the line. Sometimes children are severely affected.

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