Search results
Results from the WOW.Com Content Network
Stephen Stone, past president of the American Academy of Dermatology, confirmed that this was Lewandowsky–Lutz. [citation needed] Toader underwent surgery in late 2013, and since then has been mostly symptom-free, with only small reappearances.
With Jadassohn, he described an ectodermal dysplasia now known as Jadassohn–Lewandowsky syndrome. Just prior to his death, he described epidermodysplasia verruciformis, a rare skin disorder sometimes known as "Lewandowsky–Lutz dysplasia" (named along with dermatologist Wilhelm Lutz 1888–1958). [2] He died on 31 October 1921 in Basel.
This is a list of diseases starting with the letter "L". ... Lutz–Richner–Landolt syndrome; Lutz–Lewandowsky epidermodysplasia verruciformis; Ly
An eponymous disease is a disease, disorder, condition, or syndrome named after a person, usually the physician or other health care professional who first identified the disease; less commonly, a patient who had the disease; rarely, a literary character who exhibited signs of the disease or an actor or subject of an allusion, as characteristics associated with them were suggestive of symptoms ...
Pachyonychia congenita type I (also known as "Jadassohn–Lewandowsky syndrome" [9]) is an autosomal dominant keratoderma that principally involves the plantar surfaces, but also with nails changes that may be evident at birth, but more commonly develop within the first few months of life. [8]: 510 [9] [10]: 569
Lutz-Splendore-de Almeida disease [3] is named for the physicians Adolfo Lutz, [27] Alfonso Splendore (1871–1953), an Italo-Brazilian parasitologist [28] and Floriano Paulo de Almeida (1898–1977), a Brazilian pathologist specializing in Pathologic Mycology (Study of Infectious Fungi), [29] [30] who first characterized the disease in Brazil ...
She reveals her name is Lydia, and that she is looking for a man named Lujon, who is supposed to be finding a second Philosopher's Stone to save the people of their village from the return of a plague. This illness looks similar to Epidermodysplasia verruciformis (also called Lewandowsky–Lutz dysplasia, colloquially known as tree man illness ...
Sézary disease, or Sézary syndrome, [1] is a type of cutaneous T-cell lymphoma that was first described by Albert Sézary. [2] The affected T cells, known as Sézary's cells or Lutzner cells, have pathological quantities of mucopolysaccharides. Sézary disease is sometimes considered a late stage of mycosis fungoides with lymphadenopathy. [3] [4]