G475(P) Cenani-lenz syndactyly in siblings with a novel homozygous LRP4 mutation and recurrent hypoglycaemia. (25th October 2020)

• Record Type: Journal Article
• Authors: Steel, E; Hurst, J; Cullup, T; Calder, A; Sivakumar, B; Shah, P; Wilson, L
• Is Part Of: Archives of disease in childhood. Volume 105(2020)Supplement 1
• Page Start: A170
• Page End: A170
• Publication Date: 2020-10-25
• Subjects: Children -- Diseases -- Periodicals; Infants -- Diseases -- Periodicals; 618.920005
• DOI: 10.1136/archdischild-2020-rcpch.407
• Languages: English
• ISSNs: 0003-9888

Abstract

Abstract : Cenani-Lenz Syndactyly (CLS) is a rare autosomal recessive syndrome characterized by disorganized oligosyndactyly of upper and lower limbs as well as radioulnar synostosis. Structural renal abnormalities are also common. We report two affected brothers, born to orthodox Jewish parents, in whom we found a novel homozygous missense variant c.4910G>A; p.(Cys1637Tyr) in LRP4 situated in an EGF-like domain between the 4th beta-propeller and transmembrane domains. Both brothers have had recurrent ketotic hypoglycaemia which has not been associated previously. We present 3D-CT imaging illustrating the limb abnormalities in detail.