A rare case of unilateral adrenal hyperplasia accompanied by hypokalaemic periodic paralysis caused by a novel dominant mutation in CACNA1S: features and prognosis after adrenalectomy

[1] Jiang SB(2014)A retrospective study of laparoscopic unilateral adrenalectomy for primary hyperaldosteronism caused by unilateral adrenal hyperplasia Int Urol Nephrol 46 1283-1288

[2] Guo XD(2012)Unilateral adrenal hyperplasia is a usual cause of primary hyperaldosteronism. Results from a Swedish screening study BMC Endocr Disord 12 17-1255

[3] Wang HB(2012)Unilateral adrenal hyperplasia: a novel cause of surgically correctable primary hyperaldosteronism Surgery 152 1248-4041

[4] Gong RZ(1996)Paralytic myopathy-a leading clinical presentation for primary aldosteronism in Taiwan J Clin Endocrinol Metab 81 4038-380

[5] Xiong H(1995)Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder Am J Hum Genet 56 374-1099

[6] Wang Z(2001)Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A Brain 124 1091-272

[7] Zhang HY(1994)Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families Nat Genet 6 267-1936

[8] Jin XB(1999)A novel sodium channel mutation in a family with hypokalemic periodic paralysis Neurology 53 1932-1188

[9] Sigurjonsdottir HA(1997)Hypokalemia-consequences, causes, and correction J Am Soc Nephrol 8 1179-217

[10] Gronowitz M(2013)Clinical and biochemical spectrum of hypokalemic paralysis in North: East India Ann Indian Acad Neurol 16 211-336

[1] Jiang SB(2014)A retrospective study of laparoscopic unilateral adrenalectomy for primary hyperaldosteronism caused by unilateral adrenal hyperplasia Int Urol Nephrol 46 1283-1288

[2] Guo XD(2012)Unilateral adrenal hyperplasia is a usual cause of primary hyperaldosteronism. Results from a Swedish screening study BMC Endocr Disord 12 17-1255

[3] Wang HB(2012)Unilateral adrenal hyperplasia: a novel cause of surgically correctable primary hyperaldosteronism Surgery 152 1248-4041

[4] Gong RZ(1996)Paralytic myopathy-a leading clinical presentation for primary aldosteronism in Taiwan J Clin Endocrinol Metab 81 4038-380

[5] Xiong H(1995)Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder Am J Hum Genet 56 374-1099

[6] Wang Z(2001)Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A Brain 124 1091-272

[7] Zhang HY(1994)Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families Nat Genet 6 267-1936

[8] Jin XB(1999)A novel sodium channel mutation in a family with hypokalemic periodic paralysis Neurology 53 1932-1188

[9] Sigurjonsdottir HA(1997)Hypokalemia-consequences, causes, and correction J Am Soc Nephrol 8 1179-217

[10] Gronowitz M(2013)Clinical and biochemical spectrum of hypokalemic paralysis in North: East India Ann Indian Acad Neurol 16 211-336