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Autoimmune diabetes
Diabetes
Diabetes mellitus type 1
Growth-onset diabetes
IDDM
Insulin-dependent diabetes
Insulin-dependent diabetes mellitus
Juvenile arthritis with systemic onset
Juvenile diabetes
Juvenile-onset
Juvenile-onset diabetes
Juvenile-onset diabetes mellitus
Ketosis-prone
Ketosis-prone diabetes
Polyarticular onset juvenile idiopathic arthritis
Polyarticular onset juvenile rheumatoid arthritis
Still's disease
Systemic juvenile idiopathic arthritis
Systemic-onset juvenile chronic arthritis
Systemic-onset juvenile rheumatoid arthritis
Type 1 diabetes
Type I
Type I diabetes
Type I diabetes mellitus

Traduction de « juvenile-onset optic » (Anglais → Français) :

A rare endocrine disease with characteristics of the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy

syndrome de Wolfram-like


insulin-dependent diabetes mellitus [ IDDM | type I diabetes mellitus | diabetes mellitus type 1 | juvenile-onset diabetes | growth-onset diabetes | type 1 diabetes | juvenile diabetes | juvenile-onset diabetes mellitus | ketosis-prone diabetes | autoimmune diabetes ]

diabète insulino-dépendant [ DID | diabète insulinodépendant | diabète type 1 | diabète maigre | diabète de l'enfant | diabète juvénile ]


Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s

ataxie spinocérébelleuse type 28


insulin-dependent diabetes | juvenile-onset diabetes | type I diabetes

diabète de type I | diabète insulino-dépendant | diabète juvénile | diabète maigre | DT1 | DID [Abbr.]


A genetic neurodegenerative disease with normal early development followed by childhood onset optic atrophy with progressive vision loss and eventually blindness, followed by progressive neurological decline that typically includes cerebellar ataxia,

syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité


diabetes (mellitus):brittle | juvenile-onset | ketosis-prone | type I

diabète (sucré):instable | juvénile | sujet à cétose | type I


Still's disease | systemic juvenile idiopathic arthritis | systemic-onset juvenile chronic arthritis | systemic-onset juvenile rheumatoid arthritis

arthrite rhumatoïde de l'enfant | maladie de Still


polyarticular onset juvenile idiopathic arthritis | polyarticular onset juvenile rheumatoid arthritis

arthrite juvénile idiopathique polyarticulaire active


Juvenile arthritis with systemic onset

Arthrite juvénile avec début systémique


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