Table 6 Clinical details of children with no genetic variant
From: Clinical utility of genetic testing in Indian children with kidney diseases
Case | Age in mo | Sex | Family History | Disease Category | Clinical Diagnosis |
|---|---|---|---|---|---|
9 | 60 | M | Nil | 1 | Tubulopathy |
37 | 108 | M | Nil | 1 | Proximal RTA |
61 | 84 | M | Nil | 1 | Dent Disease |
18 | 84 | M | Nil | 2 | SRNS/FSGS |
8 | 60 | F | Nil | 2 | SRNS/FSGS |
23 | 60 | F | Nil | 2 | SRNS/FSGS |
33 | 48 | M | Nil | 2 | SRNS/FSGS |
39 | 84 | M | Nil | 2 | SRNS/FSGS |
45 | 48 | M | Nil | 2 | SRNS/FSGS |
50 | 24 | M | Nil | 2 | SRNS/FSGS |
58 | 24 | M | Nil | 2 | SRNS/FSGS |
74 | 12 | M | Nil | 2 | SRNS/FSGS |
20 | 192 | M | Nil | 4 | Syndromic CAKUT |
10 | 132 | M | Yes, younger brother had similar complain of CKD and retinitis pigmentosa | 5 | Senior Loken Syndrome |
55 | 168 | F | Nil | 6 | CKD |
54 | 132 | F | Nil | 6 | CKD |
41 | 48 | M | Nil | 8 | Idiopathic infantile calcinosis |