📂 Diseases
fatal infantile hypertonic myofibrillar myopathy — Definition
Ölümcül infantil hipertonik miyofibriler miyopati / fatal infantile hypertonic myofibrillar myopathy
This disease is a rare genetic muscle disorder, characterized by excessive increase (hypertoni) in childhood and muscle tone. Miofibriler develops muscle weakness and respiratory failure as a result of disruption of structures. Usually, in the first year of life, there is a fatal watcher and autozomal resesif inheritance.
Frequently Asked Questions
❓ What is Ölümcül infantil hipertonik miyofibriler miyopati?
Ölümcül infantil hipertonik miyofibriler miyopati; this disease is a rare genetic muscle disorder, characterized by excessive increase (hypertoni) in childhood and muscle tone. Miofibriler develops muscle weakness and respiratory failure as a result of disruption of structures. Usually, in the first year of life, there is a fatal watcher and autozomal resesif inheritance.
❓ What is fatal infantile hypertonic myofibrillar myopathy in Turkish?
The Turkish equivalent of "fatal infantile hypertonic myofibrillar myopathy" is Ölümcül infantil hipertonik miyofibriler miyopati.
❓ Which medical field is Ölümcül infantil hipertonik miyofibriler miyopati related to?
This term belongs to the Diseases category.