📂 Diseases
intellectual disability, autosomal recessive 59; MRT59 — Definition
Otozomal Resesif 59 Zihinsel Yetersizlik; MRT59 / intellectual disability, autosomal recessive 59; MRT59
Otozomal resesif is a rare genetic disease, showing transition. The disease is characterized by additional neurological findings such as mental insufficiency, development backrest and some cases of seizures, motion disorders or facial anomalies. MRT59 occurs as a result of a specific gene mutation and is often pronounced in childhood. The diagnosis, clinical evaluation and genetic tests are performed; treatment involves supporting care for symptoms.
Frequently Asked Questions
❓ What is Otozomal Resesif 59 Zihinsel Yetersizlik; MRT59?
Otozomal Resesif 59 Zihinsel Yetersizlik; MRT59; otozomal resesif is a rare genetic disease, showing transition. The disease is characterized by additional neurological findings such as mental insufficiency, development backrest and some cases of seizures, motion disorders or facial anomalies. MRT59 occurs as a result of a specific gene mutation and is often pronounced in childhood. The diagnosis, clinical evaluation and genetic tests are performed; treatment involves supporting care for symptoms.
❓ What is intellectual disability, autosomal recessive 59; MRT59 in Turkish?
The Turkish equivalent of "intellectual disability, autosomal recessive 59; MRT59" is Otozomal Resesif 59 Zihinsel Yetersizlik; MRT59.
❓ Which medical field is Otozomal Resesif 59 Zihinsel Yetersizlik; MRT59 related to?
This term belongs to the Diseases category.