Vertaling van "sotos syndrome " (Engels → Nederlands) :

cerebral gigantism | Sotos syndrome
cerebraal gigantisme | Sotos syndroom

Syndrome:Beckwith-Wiedemann | Sotos | Weaver
syndroom van | Beckwith-Wiedemann | syndroom van | Sotos | syndroom van | Weaver

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 symptoms, clinical signs and behaviour, and other evidence such as a drug being in the patient's possession or reports from informed third parties. Many drug users take more than one type of psychoactive substance. The main diagnosis should be classified, whenever possible, according to the substance or class of substances that has caused or contributed most to the presenting clinical syndrome. Other diagnoses should be coded when other psychoactive substances have been taken in intoxicating amounts (common fourth character .0) or to the extent of causing harm (common fourth character .1), dependence (common fourth character .2) or other disorders (common fourth character .3-.9). Only in cases in which patterns of psychoactive substance-taking are chaotic and indiscriminate, or in which the contributions of different psychoactive substances are inextricably mixed, should the diagnosis of disorders resulting from multiple drug use (F19.-) be used. | Modifiers The following fourth-character subdivisions are for use with categories F10-F19: Code Title .0 Acute intoxication A condition that follows the administration of a psychoactive substance resulting in disturbances in level of consciousness, cognition, perception, affect or behaviour, o ...
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

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

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

syndrome
syndroom | ziektebeeld