Article
Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities.
Genetics in medicine : official journal of the American College of Medical Genetics - 1 Jan 2023
Cali Elisa, Suri Mohnish, Scala Marcello, Ferla Matteo P, Alavi Shahryar, Faqeih Eissa Ali, Bijlsma Emilia K, Wigby Kristen M, Baralle Diana, Mehrjardi Mohammad Y V, Schwab Jennifer, Platzer Konrad, Steindl Katharina, Hashem Mais, Jones Marilyn, Niyazov Dmitriy M, Jacober Jennifer, Littlejohn Rebecca Okashah, Weis Denisa, Zadeh Neda, Rodan Lance, Goldenberg Alice, Lecoquierre François, Dutra-Clarke Marina, Horvath Gabriella, Young Dana, Orenstein Naama, Bawazeer Shahad, Vulto-van Silfhout Anneke T, Herenger Yvan, Dehghani Mohammadreza, Seyedhassani Seyed Mohammad, Bahreini Amir, Nasab Mahya E, Ercan-Sencicek A Gulhan, Firoozfar Zahra, Movahedinia Mojtaba, Efthymiou Stephanie, Striano Pasquale, Karimiani Ehsan Ghayoor, Salpietro Vincenzo, Taylor Jenny C, Redman Melody, Stegmann Alexander P A, Laner Andreas, Abdel-Salam Ghada, Li Megan, Bengala Mario, Müller Amelie Johanna, Digilio Maria C, Rauch Anita, Gunel Murat, Titheradge Hannah, Schweitzer Daniela N, Kraus Alison, Valenzuela Irene, McLean Scott D, Phornphutkul Chanika, Salih Mustafa, Begtrup Amber, Schnur Rhonda E, Torti Erin, Haack Tobias B, Prada Carlos E, Alkuraya Fowzan S, Houlden Henry, Maroofian Reza
Abstract excerpt
PURPOSE: Protein arginine methyltransferase 7 (PRMT7) is a member of a family of enzymes that catalyzes the methylation of arginine residues on several protein substrates. Biallelic pathogenic PRMT7 variants have previously been associated with a syndromic neurodevelopmental disorder characterized by short stature, brachydactyly, intellectual developmental disability, and seizures. To our knowledge, no...
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