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In questa pagina puoi ottenere un'analisi dettagliata di una parola o frase, prodotta utilizzando la migliore tecnologia di intelligenza artificiale fino ad oggi:
- come viene usata la parola
- frequenza di utilizzo
- è usato più spesso nel discorso orale o scritto
- opzioni di traduzione delle parole
- esempi di utilizzo (varie frasi con traduzione)
- etimologia
Cosa (chi) è lipoid - definizione
lipoid
WIKIMEDIA DISAMBIGUATION PAGE
Lipoid (disambiguation)
['l?p??d]
¦ adjective Biochemistry relating to or resembling fat.
Origin
C19: from Gk lipos 'fat' + -oid.
Minimal change disease
![[[Periorbital edema]] that can be seen in minimal change disease](https://commons.wikimedia.org/wiki/Special:FilePath/Nephrotic eyes.JPG?width=200 "[[Periorbital edema]] that can be seen in minimal change disease")
HUMAN DISEASE
Lipoid nephrosis; Nephrosis, lipoid; Minimal Change Disease; Minimal change nephropathy; Minimal change lesion; Minimal change glomerulonephritis; Minimal-change disease; Nil lesion; Nil disease
Minimal change disease (also known as MCD, minimal change glomerulopathy, and nil disease, among others) is a disease affecting the kidneys which causes a nephrotic syndrome. Nephrotic syndrome leads to the loss of significant amounts of protein in the urine, which causes the widespread edema (soft tissue swelling) and impaired kidney function commonly experienced by those affected by the disease.
Urbach–Wiethe disease
![q]]21](https://commons.wikimedia.org/wiki/Special:FilePath/Chromosome 1.svg?width=200 "q]]21")
RARE RECESSIVE GENETIC DISORDER
Lipoid proteinosis; Lipoid proteinosis of Urbach and Wiethe; Urbach-Wiethe Disease; Hyalinosis cutis et mucosae; Urbach-Wiethe; Urbach-Wiethe disease; Urbach Wiethe disease; Bilateral intracranial sickle-shaped calcification of the temporal lobes; Bilateral intracranial sickle-shaped calcifications of the temporal lobes; Urbach-wiethe syndrome; Urbach-Wieth disease
Urbach–Wiethe disease is a very rare recessive genetic disorder, with approximately 400 reported cases since its discovery. It was first officially reported in 1929 by Erich Urbach and Camillo Wiethe, although cases may be recognized dating back as early as 1908.
