Lowe Syndrome - Case Report with a Novel Mutation in the Oculocerebrorenal Gene

Sethi, S; Sethi, N; Mehta, S; Kaur, S; Makkar, V; Sohal, PM

Mehta, S (corresponding author), Dayanand Med Coll & Hosp, Dept Nephrol, Ludhiana, Punjab, India.

SAUDI JOURNAL OF KIDNEY DISEASES AND TRANSPLANTATION, 2020; 31 (1): 285

Abstract

The oculocerebrorenal (OCRL) syndrome, also known as Lowe syndrome (LS), is an X-linked recessive disorder that predominantly affects males and is cha......

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