TY - JOUR
T1 - PUS3-related disorder
T2 - Report of a novel patient and delineation of the phenotypic spectrum
AU - Borghesi, Alessandro
AU - Plumari, Massimo
AU - Rossi, Elena
AU - Viganò, Claudia
AU - Cerbo, Rosa Maria
AU - Codazzi, Alessia Claudia
AU - Valente, Enza Maria
AU - Gana, Simone
N1 - © 2021 Wiley Periodicals LLC.
PY - 2022/10/29
Y1 - 2022/10/29
N2 - PUS3 encodes the pseudouridylate synthase 3, an enzyme catalyzing the formation of tRNA pseudouridine, which plays a critical role in tRNA structure, function, and stability. Biallelic pathogenic variants of PUS3 have been previously associated with severe intellectual disability, microcephaly, epilepsy, and short stature. We identified a novel homozygous PUS3 frameshift variant in a child with facial dysmorphisms, growth failure, microcephaly, retinal dystrophy, cerebellar hypoplasia, congenital heart defect, and right kidney hypoplasia. This patient further expands the phenotypic spectrum of PUS3-related disorders to include a more severe syndromic presentation.
AB - PUS3 encodes the pseudouridylate synthase 3, an enzyme catalyzing the formation of tRNA pseudouridine, which plays a critical role in tRNA structure, function, and stability. Biallelic pathogenic variants of PUS3 have been previously associated with severe intellectual disability, microcephaly, epilepsy, and short stature. We identified a novel homozygous PUS3 frameshift variant in a child with facial dysmorphisms, growth failure, microcephaly, retinal dystrophy, cerebellar hypoplasia, congenital heart defect, and right kidney hypoplasia. This patient further expands the phenotypic spectrum of PUS3-related disorders to include a more severe syndromic presentation.
U2 - 10.1002/ajmg.a.62547
DO - 10.1002/ajmg.a.62547
M3 - Article
C2 - 34713961
SN - 1552-4825
JO - Am. J. Med. Genet. Part A
JF - Am. J. Med. Genet. Part A
ER -