Osler-Weber-Rondu syndrome (Hereditary Hemorrhagic Telangiectasia): Difference between revisions
Ttenbergen (talk | contribs) m Text replacement - "Alternate ICD10s to consider coding instead" to "Alternate ICD10s to consider coding instead or in addition" |
Ttenbergen (talk | contribs) m Text replacement - "Gastritis, hemorragic" to "Gastritis, hemorrhagic" |
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== Additional Info == | == Additional Info == | ||
Osler-Weber-Rondu syndrome (Hereditary Hemorrhagic Telangiectasia / HHT) is a rare autosomal dominant genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membranes, and often in organs such as the lungs, liver, and brain. | |||
Telangiectasia (small vascular malformations) may occur in the skin and mucosal linings of the nose and gastrointestinal tract. | Telangiectasia (small vascular malformations) may occur in the skin and mucosal linings of the nose and gastrointestinal tract. | ||
[[Arteriovenous malformation (AVM)]] is an abnormal connection between arteries and veins, bypassing the capillary system. This vascular anomaly is widely known because of its occurrence in the central nervous system (usually [[Arteriovenous malformation (AVM)]]), but can appear in any location. Although many AVMs are asymptomatic, they can cause intense pain or bleeding or lead to other serious medical problems. | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||
*[[Disorder of nose and/or sinuses, infectious or noninfectious NOS]] | |||
*[[Gastritis, hemorrhagic]] | |||
*[[Gastritis, NOS]] | |||
*[[Cerebral aneurysm, nonruptured]] | |||
*[[Hemorrhage, subarachnoid or ruptured cerebral aneurysm]] | |||
== Candidate [[Combined ICD10 codes]] == | |||
== Related CCI Codes == | |||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
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