Category:Rett syndrome

From Wikimedia Commons, the free media repository
Jump to navigation Jump to search
<nowiki>síndrome de Rett; síndrome de Rett; Rett-Syndrom; سندروم رت; 蕾特氏症; Rett syndrom; რეტის სინდრომი; レット症候群; Retts syndrom; תסמונת רט; 蕾特氏症; 雷特综合征; Rettin oireyhtymä; ৰেট চিণ্ড্ৰোম; sindromo de Rett; Rettův syndrom; இரெட் நோய்த்தொகை; sindrome di Rett; syndrome de Rett; Retti sündroom; 레트 증후군; Σύνδρομο Ρετ; Ретов синдром; Retov sindrom; Rett sendromu; Ретов синдром; Hội chứng Rett; síndrome de Rett; Reta sindroms; синдром Ретта; Ретов синдром; Syndroom van Rett; Синдром Ретта; Rettov sindrom; กลุ่มอาการเรตต์; Sindrom Rett; zespół Retta; Retts syndrom; 蕾特氏症; Ռետտի համախտանիշ; ରେଟ ସିଣ୍ଡ୍ରୋମ; Rettov sindrom; Syndrom Rett; Rett syndrome; متلازمة ريت; 雷特综合征; Rett sindromi; malattia rara; 神経疾患の一つ; une maladie génétique rare se développant chez le très jeune enfant, principalement la fille, et provoquant un handicap mental et des atteintes motrices sévères; Penyakit genetik yang menyebabkan gen MECP2 bermutasi yang hanya menyerang perempuan; genetycznie uwarunkowane zaburzenie neurologiczne; arvelig utviklingsforstyrrelse i hjernen; Neurologische ziekte; психоневрологическое наследственное заболевание; genetika neŭrologia malsano; neurologische Erkrankung; erittäin harvinainen neurologinen sairaus; genetic brain disorder; مرض يصيب الإنسان; вродено пореметување на мозокот; תסמונת המאופיינת בניוון התפתחותי פרוגרסיבי; Disturbo di Rett; Sindrome CDKL5; Sindrome di Rett atipica; レット障害; Syndrome de Reth; Rett syndrom; Ретта синдром; Rett syndrom; RS; cerebroatrofisk hyperammonemi; Stoornis van Rett; Rettsyndroom; Ретта синдром; Σύνδρομο Rett; Sindrome de Rett; trastorno de Rett; Rett-oireyhtymä; Rettin syndrooma; Rett-syndrooma; Rett's disorder; cerebroatrophic hyperammonemia; atypical Rett syndrome; Rett's syndrome; trastorn de Rett; 瑞特氏症候群; 雷特氏症; 雷特氏症候群; Rett综合征; 雷特综合征; Rettov sindrom; Syndroma Rett</nowiki>
Rett syndrome 
genetic brain disorder
A 15-year-old female with Rett syndrome and severe scoliosis.
Upload media
Instance of
  • designated intractable/rare disease
  • rare disease
  • class of disease
Subclass of
Named after
Discoverer or inventor
Time of discovery or invention
  • 1966
Authority file
Wikidata Q917357
GND ID: 4260313-4
Library of Congress authority ID: sh86003783
NDL Authority ID: 001137110
BNCF Thesaurus ID: 5040
NL CR AUT ID: ph330263
BabelNet ID: 03372045n
National Library of Israel J9U ID: 987007553776705171
Edit infobox data on Wikidata

Rett syndrome is a pervasive developmental disorder.

Media in category "Rett syndrome"

The following 6 files are in this category, out of 6 total.