LRP4 site-specific variants in the third β-propeller domain causes congenital myasthenic syndrome type 17

• Published in: European journal of medical genetics Vol. 67; p. 104903
• Main Authors: Al Jabry, Tariq, Al-Hashmi, Nadia, Abdelhadi, Basem, Al-Maawali, Almundher
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Masson SAS 01.02.2024
• Subjects: Acetylcholine receptors; Agrin; CMS17; Congenital myasthenic syndromes; Female; Humans; Hyperostosis; Infant, Newborn; LDL-Receptor Related Proteins - genetics; LRP4; Male; Myasthenic Syndromes, Congenital - genetics; Neuromuscular Junction; Syndactyly - genetics; Congenital myasthenic syndromes; LRP4; CMS17; Agrin; Neuromuscular junction; Acetylcholine receptors
• ISSN: 1769-7212; 1878-0849
• DOI: 10.1016/j.ejmg.2023.104903

LRP4 is expressed in many organs. It mediates SOST-dependent inhibition of bone formation and acts as an inhibitor of WNT signaling. It is also a postsynaptic end plate cell surface receptor at the neuromuscular junction and is central to its development, maintenance, and function. Pathogenic variants of LRP4 that specifically affect the canonical WNT signaling pathway are known to be associated with Cenani-Lenz syndactyly syndrome or the overlapping condition sclerosteosis. However, site-specific pathogenic variants of LRP4 have been associated with the congenital myasthenic syndrome (CMS) type 17 with no abnormal bone phenotype. Only two studies reported biallelic variants of LRP4 associated with CMS17 that presented during childhood. All three reported variants (NM_002334.4: p.Glu1233Ala, p.Glu1233Lys, or p.Arg1277His) are located within the 3′-edge of the third β-propeller domain of LRP4. We report on a patient with a biallelic variant of the LRP4 gene presenting with a severe and neonatal lethal phenotype; we also provide a literature review of the previously reported patients. A female neonate, born to healthy consanguineous parents, presented with severe hypotonia, congenital diaphragmatic hernia, pulmonary hypertension, and progressive hypoxemia. Two of her siblings presented with a similar condition in the past, and all three died shortly after birth. Clinical exome sequencing revealed homozygosity for the pathogenic variant NM_002334.4:c.3698A > C (p.[Glu1233Ala]).