Sack-Barabas syndrome, abbreviated SBS, is an older name for vascular Ehlers-Danlos syndrome, abbreviated vEDS. It is a medical condition and a subset of the wider Ehlers-Danlos group of connective tissue disorders, distinguished by the way it especially affects the vascular system of the body. Blood vessels and organs are involved, and the tissues concerned are prone to rupture, which is the feature that sets this form apart from other kinds of Ehlers-Danlos syndrome. As an older name, it is the label found in earlier writing, while the vascular Ehlers-Danlos label is the name now given as its equivalent. This entry records the condition as a named clinical entity and is not medical advice; diagnosis and care belong to a qualified clinician.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2 Communicable or Non-communicable Prevalence Band Sources
1. Sack-Barabas syndrome (Wikipedia)
Wikipedia leadQuote, Wikipedia lead
especially affects the body's vascular system, including blood vessels and organs
View the Source 2. World Health Organization: ICD-10 Version:2019 - Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
World Health OrganizationCategory Q79.6Quote, Category Q79.6
Q79.6 Ehlers-Danlos syndrome
View the Source 3. Monarch Initiative: Ehlers-Danlos syndrome, vascular type - Monarch Initiative MONDO:0017314
Monarch InitiativeDisease descriptionQuote, Disease description
Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS.
View the Source 4. Orphadata (Orphanet): Orphadata epidemiology for ORPHA:286 Vascular Ehlers-Danlos syndrome
Orphadata (Orphanet)Prevalence, WorldwideQuote, Prevalence, Worldwide
"PrevalenceClass": "1-9 / 100 000", "PrevalenceGeographic": "Worldwide"
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