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Alcoholic hallucinosis
Autism
Autistic disorder
Autistic disorder Infantile autism
Basal cell naevus syndrome
Basal cell nevus syndrome
Building safety
Child autism
Chronic alcoholism Dipsomania Drug addiction
Delirium tremens
Disorder of personality and behaviour
FRAX
FRAXA syndrome
FXS
Fra-X syndrome
Fragile X syndrome
Fragile x chromosome syndrome
Gorlin syndrome
Gorlin-Goltz syndrome
Growth hormone
Infantile autism
Insufficiency NOS
Jealousy
Kanner syndrome
Kanner's syndrome
Martin-Bell syndrome
Paranoia
Pituitary hormone
Psychoactive substance abuse
Psychosis
Psychosis NOS
SBS
Sheehan's syndrome Simmonds' disease
Short stature
Sick building syndrome

Vertaling van "Kanner's syndrome " (Engels → Nederlands) :

Definition: A type of pervasive developmental disorder that is defined by: (a) the presence of abnormal or impaired development that is manifest before the age of three years, and (b) the characteristic type of abnormal functioning in all the three areas of psychopathology: reciprocal social interaction, communication, and restricted, stereotyped, repetitive behaviour. In addition to these specific diagnostic features, a range of other nonspecific problems are common, such as phobias, sleeping and eating disturbances, temper tantrums, and (self-directed) aggression. | Autistic disorder Infantile:autism | psychosis | Kanner's syndrome

Omschrijving: Een pervasieve ontwikkelingsstoornis die is gedefinieerd door: a) de aanwezigheid van een afwijkende of beperkte ontwikkeling die aan het licht treedt voor het derde levensjaar en b) kenmerkend afwijkend-functioneren op alle drie psychopathologische terreinen: sociale interactie; communicatie; en beperkt, stereotiep zich herhalend gedrag. Naast deze specifieke diagnostische-kenmerken komt vaak een reeks andere niet-specifieke problemen voor, zoals fobieën, slaap- en eetstoornissen, temper tantrums en (tegen zichzelf gerichte) agressie. | Neventerm: | autistische stoornis | infantiel autisme | infantiele psychose | syndroom van Kanner


autism | autistic disorder | child autism | infantile autism | Kanner syndrome

autisme | autismus infantum | autistische stoornis | syndroom van Kanner


fragile x chromosome syndrome | fragile X syndrome | Fra-X syndrome | FRAXA syndrome | Martin-Bell syndrome | FRAX [Abbr.] | FXS [Abbr.]

fragiel-X-syndroom | FXS [Abbr.]


basal cell naevus syndrome | basal cell nevus syndrome | Gorlin syndrome | Gorlin-Goltz syndrome

basocellulair naevussyndroom


Definition: This block contains a wide variety of disorders that differ in severity and clinical form but that are all attributable to the use of one or more psychoactive substances, which may or may not have been medically prescribed. The third character of the code identifies the substance involved, and the fourth character specifies the clinical state. The codes should be used, as required, for each substance specified, but it should be noted that not all fourth character codes are applicable to all substances. Identification of the psychoactive substance should be based on as many sources of information as possible. These include self-report data, analysis of blood and other body fluids, characteristic physical and psychological symptom ...[+++]

Omschrijving: Dit blok omvat een grote verscheidenheid van stoornissen van verschillende ernst en klinische vorm, die evenwel alle aan het gebruik van een of meer psychoactieve middelen, al dan niet op medisch voorschrift, zijn toe te schrijven. De betrokken stof wordt aangegeven door middel van het derde teken van de code en het vierde teken specificeert de klinische toestand; deze codering dient, waar nodig, gebruikt te worden voor elk gespecificeerd middel, met dien verstande dat niet elk vierde teken van toepassing is op elke stof.


A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c

overgeërfde acute myeloïde leukemie


A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib

syndroom van Möbius


Fertile eunuch syndrome Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of:gonadotropin | growth hormone | pituitary hormone | Kallmann's syndrome Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary:cachexia | insufficiency NOS | short stature | Sheehan's syndrome Simmonds' disease

dwerggroei van Lorain-Levi | fertiel eunuchoïdisme | geïsoleerde deficiëntie van | ACTH | geïsoleerde deficiëntie van | gonadotropine | geïsoleerde deficiëntie van | groeihormoon | geïsoleerde deficiëntie van | hypofysair hormoon | hypofysaire | cachexie | hypofysaire | insufficiëntie NNO | hypofysaire | kleine gestalte | hypogonadotroop hypogonadisme | idiopathische groeihormoondeficiëntie | necrose van hypofyse (post partum) | panhypopituïtarisme | syndroom van Kallmann | syndroom van Sheehan | ziekte van Simmonds


Rare syndrome with the association of congenital nephrotic syndrome, ocular anomalies and microcoria. The disorder results in proteinuria with nephrotic syndrome and histological lesions marked by diffuse mesangial sclerosis. Ocular anomalies are pre

syndroom van Pierson


building safety [ SBS | sick building syndrome ]

veiligheid van gebouwen [ hygiënevoorschriften voor gebouwen ]


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