📂 Diseases
autosomal dominant hypocalcemia 1 — Definition
Otozomal dominant hipokalsemi tip 1 / autosomal dominant hypocalcemia 1
Otozomal dominant hypocalcemia type 1 is a rare genetic disease that occurs due to mutations in calcium sensor receptor (CaSR). This condition is characterized by low levels of calcium in the blood (hychoalemia), usually light or symptomatic dilut. Symptoms such as muscle cramps, tingling sensation and rarely seizures can be seen in patients. Autozomal manifests a dominant inheritance, meaning the risk of passing from a affected parent is 50%.
Frequently Asked Questions
❓ What is Otozomal dominant hipokalsemi tip 1?
Otozomal dominant hipokalsemi tip 1; otozomal dominant hypocalcemia type 1 is a rare genetic disease that occurs due to mutations in calcium sensor receptor (CaSR). This condition is characterized by low levels of calcium in the blood (hychoalemia), usually light or symptomatic dilut. Symptoms such as muscle cramps, tingling sensation and rarely seizures can be seen in patients. Autozomal manifests a dominant inheritance, meaning the risk of passing from a affected parent is 50%.
❓ What is autosomal dominant hypocalcemia 1 in Turkish?
The Turkish equivalent of "autosomal dominant hypocalcemia 1" is Otozomal dominant hipokalsemi tip 1.
❓ Which medical field is Otozomal dominant hipokalsemi tip 1 related to?
This term belongs to the Diseases category.