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. 2017 Apr 12;6(5):487–494. doi: 10.3892/br.2017.892

Table I.

Renal disease in syndromic MIDs and nsMIDs.

MID RF NL NS RC RTA BLS THFS FSGS TIN NC
MELAS Yes N N N N N N Yes N N
KSS Yes N N N Yes Yes Yes N N Yes
MDS N N N N Yes N N N N Yes
LS N N N Yes Yes N N N Yes N
CPEO Yes N N N N N N N N N
PS N N N Yes Yes N N N N N
LHON N N N N N N N N Yes N
PCQD N N Yes N N N N Yes N N
XLSA Yes N N N N N N N N N
GRACILE N N N N N N Yes N N N
MEGDEL Yes N N N N N N N N N
HUPRA Yes N N N N N N N N N
MLASA N N N N Yes N N N N N
MSL N N N N Yes N N N N N
PDHD N N N N Yes N N N N N
nsMIMODS Yes Yes Yes Yes Yes N N Yes Yes Yes

RF, renal failure; NL, nephrolithiasis; NS, nephrotic syndrome; RC, renal cysts; RTA, renal tubular acidosis; BLS, Bartter-like syndrome; TDFS, Toni-Debré-Fanconi syndrome; FSGS, focal segmental glomerulosclerosis; TIN, tubulo-interstitial nephritis (nephrophthisis); NC, nephrocalcinosis; LS, Leigh syndrome; PCQD, primary coenzyme-Q deficiency; XLSA, X-linked sideroblastic anemia; nsMIMODS, non-specific MIMODS; N, not reported.