KCNK9 imprinting syndrome-further delineation of a possible treatable disorder

• Published in: American journal of medical genetics. Part A Vol. 170A; no. 10; pp. 2632 - 2637
• Main Authors: Graham Jr, John M., Zadeh, Neda, Kelley, Melissa, Tan, Ee Shien, Liew, Wendy, Tan, Victoria, Deardorff, Matthew A., Wilson, Golder N., Sagi-Dain, Lena, Shalev, Stavit A.
• Format: Journal Article
• Language: English
• Published: United States Blackwell Publishing Ltd 01-10-2016; Wiley Subscription Services, Inc
• Subjects: Birk-Barel syndrome; cleft palate; Facies; Female; flufenamic acid; Genetic Diseases, Inborn - diagnosis; Genetic Diseases, Inborn - genetics; Genetic Diseases, Inborn - therapy; Genomic Imprinting; Humans; hypotonia; imprinting disorder; Infant; intellectual disability; K2P subfamily; K2P9.1; KCNK9; Male; mefenamic acid; Mutation; personalized medicine; Phenotype; potassium channel disorder; Potassium Channels, Tandem Pore Domain - genetics; TASK3; KCNK9; cleft palate; Birk-Barel syndrome; hypotonia; mefenamic acid; personalized medicine; K2P subfamily; TASK3; K2P9.1; imprinting disorder; flufenamic acid; potassium channel disorder; intellectual disability
• ISSN: 1552-4825; 1552-4833
• DOI: 10.1002/ajmg.a.37740

Patients with KCNK9 imprinting syndrome demonstrate congenital hypotonia, variable cleft palate, normal MRIs and EEGs, delayed development, and feeding problems. Associated facial dysmorphic features include dolichocephaly with bitemporal narrowing, short philtrum, tented upper lip, palatal abnormalities, and small mandible. This disorder maps to chromosomal region 8q24, and it is caused by a specific missense mutation 770G>A in exon 2, replacing glycine at position 236 by arginine (G236R) in the maternal copy of KCNK9 within this locus. KCNK9 (also called TASK3) encodes a member of the two pore‐ domain potassium channel (K2P) subfamily. This gene is normally imprinted with paternal silencing, thus a mutation in the maternal copy of the gene will result in disease, whereas a mutation in the paternal copy will have no effect. Exome sequencing in four new patients with developmental delay and central hypotonia revealed de novo G236R mutations. Older members of a previously reported Arab–Israeli family have intellectual disability of variable severity, persistent feeding difficulties in infancy with dysphagia of liquids and dysphonia with a muffled voice in early adulthood, generalized hypotonia, weakness of proximal muscles, elongated face with narrow bitemporal diameter, and reduced facial movements. We describe the clinical features in four recently recognized younger patients and compare them with those found in members of the originally reported Arab–Israeli family and suggest this may be a treatable disorder. © 2016 Wiley Periodicals, Inc.