Atypical tuberous myxedema: Difference between revisions
From WikiMD's Medical Encyclopedia
CSV import |
CSV import |
||
| Line 40: | Line 40: | ||
{{Cutaneous-condition-stub}} | {{Cutaneous-condition-stub}} | ||
{{dictionary-stub1}} | {{dictionary-stub1}} | ||
{{No image}} | |||
Revision as of 07:46, 10 February 2025
| [[File:|250px|alt=|]] | |
| Synonyms | N/A |
| Pronounce | |
| Field | N/A |
| Symptoms | |
| Complications | |
| Onset | |
| Duration | |
| Types | |
| Causes | |
| Risks | |
| Diagnosis | |
| Differential diagnosis | |
| Prevention | |
| Treatment | |
| Medication | |
| Prognosis | |
| Frequency | |
| Deaths | |
Atypical tuberous myxedema, also known as Jadassohn–Dosseker syndrome, is thought to represent a pure nodular variant of lichen myxedematosus.<ref name="Bolognia">{{{last}}},
Rapini, Ronald P., Dermatology: 2-Volume Set, St. Louis:Mosby, 2007, ISBN 978-1-4160-2999-1, Pages: 619,</ref>
See also
References
| Mucinosis/Lichen myxedematosus | ||||||
|---|---|---|---|---|---|---|
|
