Late-Onset Mirror Syndrome
نویسندگان
چکیده
منابع مشابه
Late-onset Bartter syndrome type II
Mutations in the ROMK1 potassium channel gene (KCNJ1) cause antenatal/neonatal Bartter syndrome type II (aBS II), a renal disorder that begins in utero, accounting for the polyhydramnios and premature delivery that is typical in affected infants, who develop massive renal salt wasting, hypokalaemic metabolic alkalosis, secondary hyperreninaemic hyperaldosteronism, hypercalciuria and nephrocalci...
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ژورنال
عنوان ژورنال: Malaysian Family Physician
سال: 2021
ISSN: 1985-207X,1985-2274
DOI: 10.51866/cr1099