A case report on pseudohypoaldosteronism with a pathogenic mutation of CA12 causes autosomal recessive isolated hyperchlorhidrosis disorder by Yousef A. Alanazi

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Case Report: Autoimmune hepatitis in a patient with pseudohypoaldosteronism type 1—insights into a rare co-occurrence by Hanan Al Thiabat, Jafar Alsheyyab, Israa Waleed Khalid, Rafeef Abdel Razzaq, Kamleh Barham, Hanaa M. Algharaibeh, Eyad Altamimi

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Difficulties in the diagnosis and management of eight infants with secondary pseudohypoaldosteronism by Fatih Günay, Zeynep Şıklar, Merih Berberoğlu

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A novel mutation in exon 9 of Cullin 3 gene contributes to aberrant splicing in pseudohypoaldosteronism type II by Leping Shao, Li Cui, Jingru Lu, Yanhua Lang, Irene Bottillo, Xiangzhong Zhao

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Case Report: Type II Bartter syndrome with a novel KCNJ1 variant in a premature neonate presenting with features of salt-wasting congenital adrenal crisis and pseudo-hypoaldosteron... by Heung-Ching Tsui, Hua Tse-Timothy Cheng, Kai-Yee Lam, Lai-Ting Leung, Ka-Nam Au, Wai-Yu Wong, Luen Yee-Sylvia Siu, Lap-Ming Wong

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