📂 Diseases
Smith–Fineman–Myers syndrome — Definition
Smith-Fineman-Myers sendromu / Smith–Fineman–Myers syndrome
Smith-Fineman-Myers syndrome is a rare genetic disorder and manifests itself with mental insufficiency, characteristic facial appearance (hypertelorism, low ears, micrognati). In patients, growth backrest, hypotonia (low muscle tone) and seizures are often reported. Genetic crossing paterni has not been fully understood, and it is thought to stay resesif connected to X. The diagnosis, clinical findings and molecular genetic tests are subject; symptomatic support therapy is applied.
Frequently Asked Questions
❓ What is Smith-Fineman-Myers sendromu?
Smith-Fineman-Myers sendromu; smith-Fineman-Myers syndrome is a rare genetic disorder and manifests itself with mental insufficiency, characteristic facial appearance (hypertelorism, low ears, micrognati). In patients, growth backrest, hypotonia (low muscle tone) and seizures are often reported. Genetic crossing paterni has not been fully understood, and it is thought to stay resesif connected to X. The diagnosis, clinical findings and molecular genetic tests are subject; symptomatic support therapy is applied.
❓ What is Smith–Fineman–Myers syndrome in Turkish?
The Turkish equivalent of "Smith–Fineman–Myers syndrome" is Smith-Fineman-Myers sendromu.
❓ Which medical field is Smith-Fineman-Myers sendromu related to?
This term belongs to the Diseases category.