📂 Diseases
Seckel syndrome 2 — Definition
Seckel sendromu 2 / Seckel syndrome 2
Seckel syndrome 2 is a rare genetic disease that is rare with intrauterine growth backrest, postpartum dwarfity, microcephalus and characteristic facial appearance. This syndrome, showing autozomal resesif, is often caused by mutations in SCKL2 gene. In patients, intelligence retardation is variable and can accompany neurological findings in some cases. Diagnosis, clinical findings and genetic tests.
Frequently Asked Questions
❓ What is Seckel sendromu 2?
Seckel sendromu 2; seckel syndrome 2 is a rare genetic disease that is rare with intrauterine growth backrest, postpartum dwarfity, microcephalus and characteristic facial appearance. This syndrome, showing autozomal resesif, is often caused by mutations in SCKL2 gene. In patients, intelligence retardation is variable and can accompany neurological findings in some cases. Diagnosis, clinical findings and genetic tests.
❓ What is Seckel syndrome 2 in Turkish?
The Turkish equivalent of "Seckel syndrome 2" is Seckel sendromu 2.
❓ Which medical field is Seckel sendromu 2 related to?
This term belongs to the Diseases category.