| | References | Symptoms | Heredity | Number of patients |
| | Shaw et al. [5] | Hypoparathyroidism, renal failure, and developmental delay | Autosomal recessive | 2 girls and 2 boys | | Bilous et al. [1] | Deafness, hypoparathyroidism, and renal dysplasia | Autosomal dominant | 2 sisters and 2 brothers | | Hasegawa et al. [7] | Deafness, hypoparathyroidism, and renal dysplasia | Autosomal dominant | 1 girl | | Watanabe et al. [8] | Deafness, hypoparathyroidism, and without renal disease | Autosomal dominant | One-month-old infant and 5 members of family | | Fujimoto et al. [9] | Deafness, hypoparathyroidism, renal dysplasia, and recurrent infarcts in basal ganglia | — | 1 boy | | Muroya et al. [4] | Deafness, hypoparathyroidism, and renal dysplasia | Autosomal dominant | 9 patients | | Aksoylar et al. [10] | Deafness, hypoparathyroidism, renal dysplasia, and psoriasis | Autosomal dominant | An 18-year-old girl | | Kato et al. [11] | Deafness, hypoparathyroidism, renal dysplasia, nephrocalcinosis, and renal tubular acidosis | Autosomal dominant | A 34-year-old woman | | Taslipinar et al. [12] | Deafness, hypoparathyroidism, renal dysplasia, and renal tubular acidosis | Autosomal dominant | A 19-year-old man |
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