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Lyell's disease
Lyell's syndrome
Lyell's syndrome scalded skin syndrome
Ritter disease
Ritter's disease
Ritter's syndrome
Scalded skin syndrome
Staphylococcal scalded skin syndrome
Staphylococcal scalded-skin syndrome
Toxic bullous epidermolysis
Toxic epidermal necrolysis
Toxic epidermal necrosis

Translation of "lyell's syndrome scalded skin syndrome " (English → French) :

toxic epidermal necrolysis | Lyell's disease | Lyell's syndrome scalded skin syndrome | toxic bullous epidermolysis | toxic epidermal necrosis

épidermolyse bulleuse toxique | dermatose bulleuse allergique | épidermolyse nécrosante suraiguë | érythrodermie bulleuse avec épidermolyse | maladie de Lyell | nécrolyse épidermique toxique | nécrose épidermique toxique | syndrome de Lyell
médecine > allergologie
médecine > allergologie


Lyell's syndrome | scalded skin syndrome | toxic epidermal necrolysis

syndrome de Lyell
IATE - Health
IATE - Health


staphylococcal scalded skin syndrome [ Ritter disease | Ritter's disease | Ritter's syndrome | staphylococcal scalded-skin syndrome | Lyell's syndrome ]

maladie de Ritter [ syndrome de Lyell ]
The Skin | Symptoms (Medicine)
Appareil cutané | Symptômes (Médecine)


Staphylococcal scalded skin syndrome

Syndrome d'épidermolyse staphylococcique du nourrisson
WORLD HEALTH ORGANIZATION ICD-10: L00
WORLD HEALTH ORGANIZATION ICD-10: L00


A Noonan-related syndrome with characteristics of facial anomalies suggestive of Noonan syndrome, a distinctive hair anomaly described as loose anagen hair syndrome, frequent congenital heart defects, distinctive skin features with darkly pigmented s

syndrome Noonan-like avec cheveux anagènes caducs
SNOMEDCT-BE (disorder) / 723444009
SNOMEDCT-BE (disorder) / 723444009


Syndrome that is characterized by silvery to leaden hair, bronze skin color in sun-exposed areas and severe neurological impairment. The syndrome was first described in 1979 in three consanguineous families. It is either congenital or develops during

maladie d'Elejalde
SNOMEDCT-BE (disorder) / 724091002
SNOMEDCT-BE (disorder) / 724091002


This syndrome has characteristics of hyperlaxity of the skin involving the entire body. It has been described in six patients. The phenotype is linked to a deficiency in vitamin K-dependent clotting factors and the syndrome has been associated with m

hyperlaxité de la peau par déficit en facteur de coagulation dépendant de la vitamine K
SNOMEDCT-BE (disorder) / 717941005
SNOMEDCT-BE (disorder) / 717941005




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lyell's syndrome scalded skin syndrome

Date index:2023-01-14 -

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