📂 Diseases
syndromic X-linked intellectual disability Claes-Jensen type — Definition
Claes-Jensen tipi sendromik X'e bağlı zihinsel yetersizlik / syndromic X-linked intellectual disability Claes-Jensen type
X is a genetic disorder caused by mutations in KDM5C gene, showing resessive transition to chromosome. In patients, moderate to severely mental insufficiency, speech delay, microcephalus and pronounced facial properties (wide forehead, flat nose bridge). It can also be accompanied by epilepsy, spastisite and behavioral problems (co-like features). This syndrome can appear light learning difficulties in carrier women while more severely watching in men.
Frequently Asked Questions
❓ What is Claes-Jensen tipi sendromik X'e bağlı zihinsel yetersizlik?
Claes-Jensen tipi sendromik X'e bağlı zihinsel yetersizlik; x is a genetic disorder caused by mutations in KDM5C gene, showing resessive transition to chromosome. In patients, moderate to severely mental insufficiency, speech delay, microcephalus and pronounced facial properties (wide forehead, flat nose bridge). It can also be accompanied by epilepsy, spastisite and behavioral problems (co-like features). This syndrome can appear light learning difficulties in carrier women while more severely watching in men.
❓ What is syndromic X-linked intellectual disability Claes-Jensen type in Turkish?
The Turkish equivalent of "syndromic X-linked intellectual disability Claes-Jensen type" is Claes-Jensen tipi sendromik X'e bağlı zihinsel yetersizlik.
❓ Which medical field is Claes-Jensen tipi sendromik X'e bağlı zihinsel yetersizlik related to?
This term belongs to the Diseases category.