📂 Diseases
facial paresis, hereditary congenital, 3 — Definition
Kalıtsal Konjenital Fasiyal Parezi, Tip 3 / facial paresis, hereditary congenital, 3
Kalıtsal congenital type 3 is a type of facial nerve felci, which is available from birth and develops due to genetic mutations. This condition is characterized by weakness or loss of movement of mimic muscles on one or both sides of the face. It usually shows autozomal dominant inheritance and can be seen with other congenital anomalies. Clinically, asymmetry in facial expressions in affected individuals can bring strong and nutrition problems in eyelid.
Frequently Asked Questions
❓ What is Kalıtsal Konjenital Fasiyal Parezi, Tip 3?
Kalıtsal Konjenital Fasiyal Parezi, Tip 3; kalıtsal congenital type 3 is a type of facial nerve felci, which is available from birth and develops due to genetic mutations. This condition is characterized by weakness or loss of movement of mimic muscles on one or both sides of the face. It usually shows autozomal dominant inheritance and can be seen with other congenital anomalies. Clinically, asymmetry in facial expressions in affected individuals can bring strong and nutrition problems in eyelid.
❓ What is facial paresis, hereditary congenital, 3 in Turkish?
The Turkish equivalent of "facial paresis, hereditary congenital, 3" is Kalıtsal Konjenital Fasiyal Parezi, Tip 3.
❓ Which medical field is Kalıtsal Konjenital Fasiyal Parezi, Tip 3 related to?
This term belongs to the Diseases category.