📂 Diseases
non-syndromic X-linked intellectual disability — Definition
Sendromik Olmayan X'e Bağlı Zihinsel Yetersizlik / non-syndromic X-linked intellectual disability
Due to genetic mutations, genes in X chromosome appear as a result of dysfunction, but a pronounced type of mental insufficiency associated with a syndromeic phenotype (for example, dysmorphic facial properties or anomaly organs). Often mild to moderate cognitive feedback is observed in patients and other systemic findings are minimal. The diagnosis is subject to family history and genetic tests; the treatment is symptomatic and supporting.
Frequently Asked Questions
❓ What is Sendromik Olmayan X'e Bağlı Zihinsel Yetersizlik?
Sendromik Olmayan X'e Bağlı Zihinsel Yetersizlik; due to genetic mutations, genes in X chromosome appear as a result of dysfunction, but a pronounced type of mental insufficiency associated with a syndromeic phenotype (for example, dysmorphic facial properties or anomaly organs). Often mild to moderate cognitive feedback is observed in patients and other systemic findings are minimal. The diagnosis is subject to family history and genetic tests; the treatment is symptomatic and supporting.
❓ What is non-syndromic X-linked intellectual disability in Turkish?
The Turkish equivalent of "non-syndromic X-linked intellectual disability" is Sendromik Olmayan X'e Bağlı Zihinsel Yetersizlik.
❓ Which medical field is Sendromik Olmayan X'e Bağlı Zihinsel Yetersizlik related to?
This term belongs to the Diseases category.