Entrez un mot ou une phrase dans n'importe quelle langue 👆
Langue:
Traduction et analyse de mots par intelligence artificielle ChatGPT
Sur cette page, vous pouvez obtenir une analyse détaillée d'un mot ou d'une phrase, réalisée à l'aide de la meilleure technologie d'intelligence artificielle à ce jour:
- comment le mot est utilisé
- fréquence d'utilisation
- il est utilisé plus souvent dans le discours oral ou écrit
- options de traduction de mots
- exemples d'utilisation (plusieurs phrases avec traduction)
- étymologie
Qu'est-ce (qui) est Xanthochromia - définition
Xanthochromia
MEDICAL CONDITION
Xanthochromic; Xanthochromasia
Xanthochromia, from the Greek xanthos (ξανθός) "yellow" and chroma (χρώμα) "colour", is the yellowish appearance of cerebrospinal fluid that occurs several hours after bleeding into the subarachnoid space caused by certain medical conditions, most commonly subarachnoid hemorrhage. Its presence can be determined by either spectrophotometry (measuring the absorption of particular wavelengths of light) or simple visual examination.
Palmoplantar keratoderma
KERATOSIS CHARACTERIZED BY ABNORMAL THICKENING OF THE PALMS AND THE SOLES
Palmo-plantar keratoderma; Palmoplantar Keratoderma; Keratoderma, palmoplantar; Sclerotylosis; Scleroatrophy; Acquired keratosis (keratoderma) palmaris et plantaris; Inherited keratosis palmaris et plantaris; Punctate palmoplantar keratoderma; Focal palmoplantar keratoderma; Diffuse palmoplantar keratoderma; Diffuse epidermolytic palmoplantar keratoderma; Diffuse epidermolytic PPK; Palmoplantar keratoderma cum degeneratione granulosa Vörner; PKK cum degeneratione granulosa Vörner; Vörner's epidermolytic palmoplantar keratoderma; Vörner's epidermolytic PPK; Diffuse nonepidermolytic palmoplantar keratoderma; Diffuse nonepidermolytic PPK; Diffuse orthohyperkeratotic keratoderma; Keratosis palmoplantaris diffusa circumscripta; Unna-Thost disease; Unna Thost disease; Striate palmoplantar keratoderma; Striate PPK; Brünauer-Fuhs-Siemens type of palmoplantar keratoderma; Keratosis palmoplantaris varians; Wachters palmoplantar keratoderma; Wachters PPK; Keratosis punctata palmaris et plantaris; Buschke-Fischer-Brauer disease; Davis Colley disease; Keratosis papulosa; Keratoderma punctatum; Maculosa disseminata; Porokeratosis punctata palmaris et plantaris; Punctate porokeratosis of the palms and soles; Focal acral hyperkeratosis; Acrokeratoelastoidosis lichenoides; Degenerative collagenous plaques of the hand; Autosomal-dominant hereditary punctate keratoderma associated with malignancy; Hereditary palmoplantar keratoderma; Palmoplantar keratoderma of Sybert; PPK of Sybert; Greither palmoplantar keratoderma; Keratosis extremitatum hereditaria progrediens; Olmsted syndrome; Mutilating palmoplantar keratoderma with periorificial keratotic plaques; Polykeratosis of Touraine; Focal palmoplantar keratoderma with oral mucosal hyperkeratosis; Hereditary painful callosity syndrome; Keratosis palmoplantaris nummularis; Vohwinkel syndrome; Keratoma hereditaria mutilans; Vohwinkel syndome; Scleroatrophic syndrome of Huriez; Huriez syndrome; Palmoplantar keratoderma with sclerodactyly; Scleroatrophic and keratotic dermatosis of the limbs; Striate palmoplantar keratoderma, woolly hair, and left ventricular dilated cardiomyopathy; Palmoplantar keratoderma and spastic paraplegia; Charcot-Marie-Tooth disease with palmoplantar keratoderma and nail dystrophy; Keratoderma disseminatum palmaris et plantaris; Keratoma hereditarium dissipatum palmare et plantare; Palmar and plantar seed dermatoses; Palmar keratoses; Punctate keratoses of the palms and soles; Aquagenic keratoderma; Acquired aquagenic syringeal acrokeratoderma; Non-epidermolytic palmoplantar keratoderma; Wachter keratoderma; Carvajal syndrome; Unna–Thost keratoderma; Unna–Thost disease; Unna-Thost keratoderma; Striate palmoplantar keratoderma, wooly hair, and left ventricular dilated cardiomyopathy; Keratoderma hereditaria mutilans; Vörner keratoderma; Aquagenic wrinkling of the palms; Acquired aquagenic palmoplantar keratoderma; Transient reactive papulotranslucent acrokeratoderma; Aquagenic syringeal acrokeratoderma; Aquagenic Keratoderma; Focal non-epidermolytic PPK; Nummular epidermolytic PPK; Focal epidermolytic PPK; Brünauer–Fuhs–Siemens PPK; Focal non-epidermolytic palmoplantar keratoderma; Palmoplantar keratoderma areata; Palmoplantar keratoderma striata; Hereditary painful callosities; Nummular epidermolytic palmoplantar keratoderma; Focal epidermolytic palmoplantar keratoderma; Mutilating palmoplantar keratoderma; Palmoplantar keratoderma with scleroatrophy; Greither syndrome; Transgrediens and progrediens palmoplantar keratoderma; Striate palmoplantar keratoderma with woolly hair and cardiomyopathy; Striate palmoplantar keratoderma with woolly hair and left ventricular dilated cardiomyopathy; Sybert keratoderma; Palmoplantar keratodermas; Sybert type; Unna-Thost type; Unna–Thost type; Greither type; Mutilating keratoderma of Vohwinkel; Brünauer–Fuhs–Siemens type of palmoplantar keratoderma; Palmoplantar keratoderma with scleroatrophy,; Charcot–Marie–Tooth disease with palmoplantar keratoderma and nail dystrophy; Buschke–Fischer–Brauer disease; Mutilating PPK with periorificial plaques; Xanthochromia striata palmaris; Spiny keratoderma; Vohwinkel's syndrome; Brünauer-Fuhs-Siemens PPK; Progressive palmoplantar keratoderma; Greither keratoderma; Mutilating palmoplantar keratoderma with periorificial plaques; Palmoplantar keratoderma with anogenital leukokeratosis; Unna-Thost syndrome; Unna's disease
Palmoplantar keratodermas are a heterogeneous group of disorders characterized by abnormal thickening of the stratum corneum of the palms and soles.
