📂 Diseases
Konigsmark-Hollander-Berlin syndrome — Definition
Konigsmark-Hollander-Berlin sendromu / Konigsmark-Hollander-Berlin syndrome
It is a rare genetic disorder, characterized by hearing loss, retinal dystrophy and diabetes starting at early age. Otozomal indicates resessive inheritance and usually gives a symptom in childhood. In patients, progressive sensorine develops hearing loss, vision disorder and insulin-dependent diabetes. Diagnostic clinical findings and genetic tests.
Frequently Asked Questions
❓ What is Konigsmark-Hollander-Berlin sendromu?
Konigsmark-Hollander-Berlin sendromu; it is a rare genetic disorder, characterized by hearing loss, retinal dystrophy and diabetes starting at early age. Otozomal indicates resessive inheritance and usually gives a symptom in childhood. In patients, progressive sensorine develops hearing loss, vision disorder and insulin-dependent diabetes. Diagnostic clinical findings and genetic tests.
❓ What is Konigsmark-Hollander-Berlin syndrome in Turkish?
The Turkish equivalent of "Konigsmark-Hollander-Berlin syndrome" is Konigsmark-Hollander-Berlin sendromu.
❓ Which medical field is Konigsmark-Hollander-Berlin sendromu related to?
This term belongs to the Diseases category.