A Rare Case of Congenital Nephrogenic Diabetes Insipidus Associated with Aquaporin 2 Gene Mutation and Subsequent Acute Lymphoblastic Leukemia: Impact of Steroids on Kidney Function

Hanan Al-Thiabat; Abdullah Abu-Aqoulah; Dana Kanaan; Mohammad Ismail Matalka; Suleimman Al-Sweedan

doi:10.12659/AJCR.943597

21 May 2024 : Case report Jordan

A Rare Case of Congenital Nephrogenic Diabetes Insipidus Associated with Aquaporin 2 Gene Mutation and Subsequent Acute Lymphoblastic Leukemia: Impact of Steroids on Kidney Function

Rare disease, Educational Purpose (only if useful for a systematic review or synthesis), Rare coexistence of disease or pathology

Hanan Al-Thiabat

^1ABCDEF*, Abdullah Abu-Aqoulah^1BC, Dana Kanaan^1BC, Mohammad Ismail Matalka^2D, Suleimman Al-Sweedan^1ABDEF

DOI: 10.12659/AJCR.943597

Am J Case Rep 2024; 25:e943597

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Introduction Case Report Discussion Conclusions References:

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Figure 2. The patient’s sodium level tracking. Arrows indicate Na level at presentation (age of 9 months), while starting DDAVP, during HCT treatment, and after starting chemotherapy. DDAVP – desmopressin; HCT – hydrochlorothiazide; ALL – acute lymphoblastic leukemia.

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A Rare Case of Congenital Nephrogenic Diabetes Insipidus Associated with Aquaporin 2 Gene Mutation and Subsequent Acute Lymphoblastic Leukemia: Impact of Steroids on Kidney Function

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