UNILATERAL KIDNEY AGENESIS IN A CHILD WITH FRASER SYNDROME: A CASE REPORT

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METANAT ZAHRA; TABATABAEI SEYED MEHDI; ZENKER MARTIN; SHAFEGHATI YOUSEF

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Paper Information

Journal: Gene, Cell and Tissue Year:2017 | Volume:4 | Issue:4 Page(s): 0-0

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Information Journal Paper

Title

UNILATERAL KIDNEY AGENESIS IN A CHILD WITH FRASER SYNDROME: A CASE REPORT

Author(s)

METANAT ZAHRA | TABATABAEI SEYED MEHDI | ZENKER MARTIN | SHAFEGHATI YOUSEF | Issue Writer Certificate

Keywords

FRASER SYNDROME

RENAL AGENESIS

UROGENITAL ABNORMALITIES

Abstract

We report a 6-year-old girl with multiple congenital anomalies compatible with FRASER SYNDROME (cryptophthalmos, syndactyly, and craniofacial abnormalities) and multiple UROGENITAL ABNORMALITIES including unilateral RENAL AGENESIS resulting from mutations in the FRAS1 gene Exon58: C.8698G-T (homozygous). The parents were heterozygous for the same mutation.

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APA: Copy

METANAT, ZAHRA, TABATABAEI, SEYED MEHDI, ZENKER, MARTIN, & SHAFEGHATI, YOUSEF. (2017). UNILATERAL KIDNEY AGENESIS IN A CHILD WITH FRASER SYNDROME: A CASE REPORT. GENE, CELL AND TISSUE, 4(4), 0-0. SID. https://sid.ir/paper/345138/en

Vancouver: Copy

METANAT ZAHRA, TABATABAEI SEYED MEHDI, ZENKER MARTIN, SHAFEGHATI YOUSEF. UNILATERAL KIDNEY AGENESIS IN A CHILD WITH FRASER SYNDROME: A CASE REPORT. GENE, CELL AND TISSUE[Internet]. 2017;4(4):0-0. Available from: https://sid.ir/paper/345138/en

IEEE: Copy

ZAHRA METANAT, SEYED MEHDI TABATABAEI, MARTIN ZENKER, and YOUSEF SHAFEGHATI, “UNILATERAL KIDNEY AGENESIS IN A CHILD WITH FRASER SYNDROME: A CASE REPORT,” GENE, CELL AND TISSUE, vol. 4, no. 4, pp. 0–0, 2017, [Online]. Available: https://sid.ir/paper/345138/en

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