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Case Reports
. 2020 Jul 3;5(9):1603-1607.
doi: 10.1016/j.ekir.2020.06.028. eCollection 2020 Sep.

Identification of a New Complement Factor H Mutation in a Patient With Pregnancy-Related Acute Kidney Injury

Domenico Santoro  1 , Antonella La Russa  2 , Giuseppina Toteda  2 , Anna Perri  2 , Donatella Vizza  2 , Simona Lupinacci  2 , Danilo Lofaro  2 , Vincenzo Pellicanò  1 , Roberta Granese  3 , Antonio Versaci  4 , Rossella Siligato  1 , Giorgina Barbara Piccoli  5   6 , Renzo Bonofiglio  2
Affiliations
Case Reports

Identification of a New Complement Factor H Mutation in a Patient With Pregnancy-Related Acute Kidney Injury

Domenico Santoro et al. Kidney Int Rep. .
No abstract available

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Figures

Figure 1
Figure 1
Trend of biochemical parameters (creatinine [a], hemoglobin [b], platelets [c], and lactate dehydrogenase [LDH; d]) after delivery.
Figure 2
Figure 2
Analysis of the splice mutation IVS12+1G>A [NM_000186.3(CFH): c.1873+1G>A]. (a) Reverse transcriptase–polymerase chain reaction from the control (C) (line 1) generated a single band of 486 bp. Reverse transcriptase–polymerase chain reaction from the patient (P) carrying a heterozygous IVS12+1G>A mutation (line 2) generated a 320-bp band that was sequenced (b) and revealed a 166-bp deletion of the 3ʹ end of exon 12. IVS, intervening sequence; MW, molecular weight.
See this image and copyright information in PMC

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