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Andersenov syndróm
Č. záznamu d050030 Dátum 06.06.2025 Typ M Tematický termín Andersenov syndróm Pozri tiež (Novšie záhlavie) Pierre Robinov syndróm
(Skutočné meno) Pierre Robinov syndróm
MDT C14.280.067.565.070C14.280.123.625.070C16.131.240.400.715.070C23.550.073.547.070 Poznámka A form of inherited long QT syndrome (or LQT7) that is characterized by a triad of potassium-sensitive periodic paralysis, VENTRICULAR ECTOPIC BEATS, and abnormal features such as short stature, low-set ears, and SCOLIOSIS. It results from mutations of KCNJ2 gene which encodes a channel protein (INWARD RECTIFIER POTASSIUM CHANNELS) that regulates resting membrane potential. predmetové heslo
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