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Qu'est-ce (qui) est hypoplasia$37023$ - définition
ADRENAL CORTICAL HYPOFUNCTION THAT IS CHARACTERIZED BY A REDUCTION IN ADRENAL GLAND FUNCTION RESULTING FROM INCOMPLETE DEVELOPMENT OF THE ADRENAL CORTEX AND HAS MATERIAL BASIS IN THE NUCLEAR RECEPTOR NR0B1 (DAX1) GENE
Adrenal hypoplasia congenita; Congenital adrenal hypoplasia; X-linked AHC; Adrenal hypoplasia; Adrenal hypoplasia congenital, X-linked
X-linked adrenal hypoplasia congenita
X-linked adrenal hypoplasia congenita is a genetic disorder that mainly affects males. It involves many endocrine tissues in the body, especially the adrenal glands.
Macular hypoplasia
MEDICAL CONDITION
Fovea hypoplasia; Foveal hypoplasia-presenile cataract syndrome; O Donnell Pappas syndrome; O'Donnell-Pappas syndrome
Macular hypoplasia (or foveal hypoplasia), is a rare medical condition involving the underdevelopment of the macula, a small area on the retina (the eye's internal surface) responsible for seeing in detail. Macular hypoplasia is often associated with albinism.
Enamel hypoplasia
![hdl = 10447/1671 }}</ref> The [[National Institutes of Health]] include a dental exam in the diagnostic protocol of [[celiac disease]].<ref name=NIHCDdiagnosis />](https://commons.wikimedia.org/wiki/Special:FilePath/Enamel celiac.jpg?width=200 "hdl = 10447/1671 }}</ref> The [[National Institutes of Health]] include a dental exam in the diagnostic protocol of [[celiac disease]].<ref name=NIHCDdiagnosis />")
HUMAN DISEASE
Turner's hypoplasia; Turner tooth; Turner's tooth
Enamel hypoplasia is a defect of the teeth in which the enamel is deficient in quantity, caused by defective enamel matrix formation during enamel development, as a result of inherited and acquired systemic condition(s). It can be identified as missing tooth structure and may manifest as pits or grooves in the crown of the affected teeth, and in extreme cases, some portions of the crown of the tooth may have no enamel, exposing the dentin.
Wikipédia
X-linked adrenal hypoplasia congenita
X-linked adrenal hypoplasia congenita is a genetic disorder that mainly affects males. It involves many endocrine tissues in the body, especially the adrenal glands.
